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Can PCR fragments be normalized for the SeqTarget System without a previous purification step?
FAQ ID -2246
表示
Can I use a 384 well plate for the KRAS and EGFR PCR kits?
FAQ ID -2296
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Can the miScript Precursor Assay differentiate between pri- and pre-miRNA?
FAQ ID -2211
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Does ethanol from the PCR product purification influence the normalization procedure for the SeqTarget System?
FAQ ID -2244
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What are EasyXtal 15-well Tools used for?
FAQ ID -2217
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What are Principal Components analyzed in Rotor-Gene ScreenClust HRM Software?
FAQ ID -2200
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What are the amplicon lengths of the KRAS and EGFR PCR kits?
FAQ ID -2289
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What are clusters analyzed in the Rotor-Gene ScreenClust HRM Software?
FAQ ID -2201
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Is the SeqTarget System compatible with standard-size PCRs?
FAQ ID -2241
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What controls are used in the KRAS and EGFR PCR kits to ensure reliable results?
FAQ ID -2291
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What does QIAGEN use for a positive control in precursor detection experiments?
FAQ ID -2212
表示
What do I do if I cannot see amplification in the FAM channel in my KRAS and EGFR PCR kits?
FAQ ID -2297
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What are the corresponding QIAGEN names for former Biotage instruments?
FAQ ID -2285
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What can be the reason for low DNA yields after normalization with the SeqTarget System?
FAQ ID -2239
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How much buffer should be used for agarose gel electrophoresis?
FAQ ID -2257
表示
How long does it take to generate results using the KRAS and EGFR PCR kits?
FAQ ID -2299
表示
How should gels be cast with the GelPilot Agarose so that optimal resolution is achieved?
FAQ ID -2258
表示
How long should PCR fragments be for the SeqTarget System?
FAQ ID -2236
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Is it possible to use lower siRNA concentrations with FlexiTube siRNA Premix?
FAQ ID -2264
表示
How many miScript Precursor Assays do you offer?
FAQ ID -2213
表示
Is one able to use FlexiTube siRNA Premix for transfection of primary adherent cell types?
FAQ ID -2268
表示
If I am working with a difficult-to-transfect cell type or if I obtain only weak silencing effects what can I do?
FAQ ID -2265
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Is one able to use FlexiTube siRNA Premix for transfection of primary suspension cell types?
FAQ ID -2269
表示
Is it possible to normalize to more or less than 500 ng with the SeqTarget System if needed?
FAQ ID -2235
表示
How many samples can be processed with the QIAsymphony DNA Mini Kit and the Virus Blood 200 protocol?
FAQ ID -2159
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How often can the Strep-Tactin Superflow Plus resin be reused?
FAQ ID -2169
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Is it possible to purify and normalize long range PCRs produced with PCR kits from other vendors for the SeqTarget System?
FAQ ID -2243
表示
If housekeeping and target genes differ significantly in abundance, will they both be amplified with equal efficiency using the Rotor-Gene Multiplex PCR Kit?
FAQ ID -2129
表示
If Vapor-Lock is used to overlay PCR reactions, which volume should be entered as reaction volume in the Rotor-Gene Q Software?
FAQ ID -2150
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Is it possible to purify a GST-tagged protein under denaturing conditions using Glutathione Superflow?
FAQ ID -2172
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Is it normal that the binding capacity of GST-resins decreases with flow rate?
FAQ ID -2174
表示
Why is the initial activation step different for Rotor-Gene Probe, SYBR Green and Multiplex Kits?
FAQ ID -2118
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Will Rotor-Gene Kits also work on the Rotor-Gene 6000 and 3000 cyclers?
FAQ ID -2121
表示
Why is there an asterisk for my miScript Primer Assays?
FAQ ID -2176
表示
Will Uracil-N-Glycosylase (UNG) completely remove contaminating amplicons when using QuantiTect +UNG Kits?
FAQ ID -2139
表示
Will QuantiTect Primer Assays work with Rotor-Gene SYBR Green Kits using an annealing step at 60ºC?
FAQ ID -2124
表示
What is miRNA*? Do I need to consider this in my profiling experiment?
FAQ ID -2179
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What are the main differences between Rotor-Gene and QuantiTect or QuantiFast PCR Kits?
FAQ ID -2119
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What are possible reasons for reduced DNA yields with REPLI-g Kits?
FAQ ID -2148
表示
What is the residuals plot in the Rotor-Gene ScreenClust HRM Software?
FAQ ID -2199
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What is the target nucleic acid for the Virus Blood 200 Protocol on the QIAsymphony?
FAQ ID -2158
表示
What is the detection limit of the Rotor-Gene and QuantiFast Multiplex RT-PCR Kits?
FAQ ID -2144
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What is the minimum number of assays that can be ordered on QuantiTect Primer Assay Plates?
FAQ ID -2109
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What is the maximum number of targets that can be amplified per reaction with the QuantiFast Multiplex RT-PCR Kit?
FAQ ID -2145
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How should DNA isolated on the QIAsymphony be stored?
FAQ ID -2165
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How should samples be stored before purification using the Virus Blood 200 Protocol on the QIAsymphony?
FAQ ID -2157
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How pure should the chloroform used with the RNeasy Microarray Tissue Mini Kit be?
FAQ ID -2193
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Why should I use the RNeasy Microarray Tissue Mini Kit when purifying RNA for microarray analysis?
FAQ ID -2188
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Which elution volumes can be selected using the QIAsymphony Virus Blood 200 protocol?
FAQ ID -2160
表示
What sample volumes can be used with the Virus Blood 200 Protocol on the QIAsymphony?
FAQ ID -2156
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Which is the best condition for eluting GST-tagged proteins from Glutathione Superflow?
FAQ ID -2173
表示
What species are QuantiTect Primer Assay Plates offered for?
FAQ ID -2110
表示
Which plate formats are offered for QuantiTect Primer Assay Plates?
FAQ ID -2106
表示
Why are the denaturation and annealing/extension times for QuantiFast Multiplex RT-PCR Kits much shorter than those for QuantiFast Multiplex PCR Kits?
FAQ ID -2147
表示
Which sample types can be processed using the QIAsymphony Virus Blood 200 protocol?
FAQ ID -2154
表示
How many reactions can be performed per well of the QuantiTect Primer Assay Plates?
FAQ ID -2107
表示
Can assays for 20 and 100 reactions be ordered on the same QuantiTect Primer Assay Plate?
FAQ ID -2108
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Can QuantiTect Primer Assay Plates be ordered offline via e-mail or fax?
FAQ ID -2112
表示
Can Glutathione Superflow resin be reused?
FAQ ID -2171
表示
Can Uracil-N-Glycosylase (UNG) be added to the QuantiTect PCR Master Mix and be stored for later use?
FAQ ID -2138
表示
Can Uracil-N-Glycosylase (UNG) be purchased separately, independent of QuantiTect PCR Kits?
FAQ ID -2134
表示
Are there any changes in the procedure using the Strep-Tactin Superflow Plus resin with the higher capacity over the standard matrix?
FAQ ID -2168
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Can Uracil-N-Glycosylase (UNG) be used with a one-step RT-PCR kit, such as the QuantiTect Probe RT-PCR Kit?
FAQ ID -2135
表示
Can the Rotor-Gene Multiplex RT-PCR Kit be used on other cyclers?
FAQ ID -2142
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Can RNA isolated with the RNeasy Microarray Tissue Mini Kit also be used in downstream applications other than microarray analysis?
FAQ ID -2191
表示
Are QuantiTect PCR +UNG Kits available in bulk format (e.g., 25 ml master mix)?
FAQ ID -2136
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Are Rotor-Gene Kits compatible with reaction setup using the QIAgility instrument?
FAQ ID -2116
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How does template quality influence the results with the Type-it HRM PCR Kit?
FAQ ID -2197
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Are the layouts for both 96- and 384-well QuantiTect Primer Assay Plates visible when ordering online?
FAQ ID -2111
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Do you have protocols for software setup on various PCR platforms using QuantiFast Probe RT-PCR Kits?
FAQ ID -2105
表示
How does magnetic-particle carry-over in QIAsymphony eluates need to be handled?
FAQ ID -2166
表示
How does the RNeasy Microarray Tissue Mini Kit prevent traces of phenol from negatively affecting the reverse-transcription step in microarray experiments?
FAQ ID -2189
表示
How do Rotor-Gene Probe Kits compare with QuantiFast Probe Kits?
FAQ ID -2125
表示
How many elution steps are recommended when using Glutathione Superflow resin?
FAQ ID -2175
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Do you have a protocol for Rotor-Gene software setup for the Rotor-Gene SYBR Green PCR and RT-PCR Kits?
FAQ ID -2104
表示
Does an internal control have to be used with the QIAsymphony Virus Blood 200 Protocol?
FAQ ID -2162
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Can Vapor-Lock be used with samples processed on the QIAgility?
FAQ ID -2153
表示
Do the master mixes in Rotor-Gene Kits contain dUTP to allow UNG pretreatment?
FAQ ID -2117
表示
Do QuantiTect Primer Assays also work with Rotor-Gene SYBR Green PCR Kits?
FAQ ID -2123
表示
Do limiting primer concentrations need to be determined when using the Rotor-Gene Multiplex PCR Kit?
FAQ ID -2128
表示
What buffer should be used to dilute cDNA made using the miScript Reverse Transcription Kit?
FAQ ID -1601
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Is FlexiTube GeneSolution available for other scales than the 1 nmol scale?
FAQ ID -1666
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Is it necessary to clean up cDNA prepared with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1610
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Is the master mix of QuantiFast Kits for real-time PCR aliquoted into several tubes to prevent cross-contamination?
FAQ ID -1697
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Is the QuantiTect Whole Transcriptome Kit suitable for miRNA amplification?
FAQ ID -1609
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Is it necessary to include a genomic DNA removal step with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1614
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Is sequence information for HP Validated siRNAs provided in the FlexiTube format?
FAQ ID -1665
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Where can I find background information and literature on Whole Genome Amplification with REPLI-g Kits?
FAQ ID -1690
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Why is there DNA in the no-template (negative) control when using the QuantiTect Whole Transcriptome Kit?
FAQ ID -1620
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What is the maximum volume of RNA in solution that can be used with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1616
表示
Can the Ni-NTA and Strep-Tactin Superflow Cartridges be reused?
FAQ ID -1607
表示
Can the Ni-NTA Superflow Cartridges and/or Strep-Tactin Cartridges be connected in series?
FAQ ID -1606
表示
Can the QuantiTect Whole Transcriptome Kit be used for amplification of RNA from LCM samples?
FAQ ID -1612
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Can I store cDNA generated by the miScript System?
FAQ ID -1602
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Does the QuantiTect Whole Transcriptome Kit work with RNA purified from bacteria, yeast, or plants?
FAQ ID -1615
表示
Can T-Script® enzyme of the QuantiTect Whole Transcriptome Kit be substituted by Quantiscript Reverse Transcriptase?
FAQ ID -1617
表示
Can the QuantiTect Whole Transcriptome reaction be stopped after the reverse transcription step to proceed with the ligation and amplification steps at a later time?
FAQ ID -1618
表示
Can I still reorder siRNA that has been removed from the GeneGlobe data base?
FAQ ID -1668
表示
Can amplification with the QuantiTect Whole Transcriptome Kit be extended to more than 8 hours to improve cDNA yields?
FAQ ID -1608
表示
Can I select HP Validated and HP GenomeWide siRNAs for FlexiTube?
FAQ ID -1658
表示
Can cDNA prepared with the QuantiTect Whole Transcriptome Kit be reampliied using REPLI-g Kits?
FAQ ID -1611
表示
Can FlexiTube siRNA or FlexiTube GeneSolution products be ordered in solution?
FAQ ID -1667
表示
How fast is the 6xHis-tagged protein purification process using Ni-NTA Superflow Cartridges?
FAQ ID -1605
表示
How long is cDNA generated with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1613
表示
How long can I archive cDNA generated with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1623
表示
Do I need to use the miScript Universal Primer for detection of mRNA?
FAQ ID -1600
表示
Have you observed co-amplification of genomic DNA from RNA templates used in the QuantiTect Whole Transcriptome Procedure?
FAQ ID -1619
表示
Do you offer a QuantiFast Kit for one-step RT-PCR?
FAQ ID -1695
表示
Do you have a protocol for purification of total RNA from plant latex?
FAQ ID -1694
表示
Do you have a protocol for purification of total RNA from plant tissue with the RNeasy Lipid Tissue Mini Kit?
FAQ ID -1693
表示
What effect does homogenization have on DNA yield and integrity when using AllPrep DNA/RNA Kits?
FAQ ID -1751
表示
Is TopTaq DNA Polymerase a hot-start polymerase?
FAQ ID -1748
表示
What is the fidelity of TopTaq DNA Polymerase?
FAQ ID -1739
表示
Which nucleotide analogs can be used with TopTaq DNA Polymerase?
FAQ ID -1741
表示
Why might Affymetrix GeneChip Mapping assays interfere with the REPLI-g FFPE kit?
FAQ ID -1755
表示
What is the shelf-life of TopTaq DNA Polymerase and Master Mix?
FAQ ID -1743
表示
What is the principle of the REPLI-g FFPE Kit?
FAQ ID -1753
表示
What is the largest plasmid size that can be purified using the QuickLyse Miniprep Kit?
FAQ ID -1752
表示
What is the minimum amount of starting material that can be used with the RNeasy Plus Micro and AllPrep DNA/RNA Micro Kit?
FAQ ID -1750
表示
What is the recommended sample size for use with the REPLI-g FFPE Kit?
FAQ ID -1756
表示
Can small miRNA-containing RNA fractions be separated from large RNAs using the miRNeasy FFPE Kit?
FAQ ID -1737
表示
Can miRNA and other RNAs smaller than 200 nucleotides be isolated with the AllPrep DNA/RNA Micro Kit or RNeasy Plus Micro Kit?
FAQ ID -1749
表示
Can TA/UA cloning be done with PCR products amplified with TopTaq DNA Polmyerase and TopTaq Master Mix Kits?
FAQ ID -1740
表示
Are there problems with the default threshold setting on the Applied Biosystems 7500 when using QuantiFast Probe PCR Kits?
FAQ ID -1702
表示
At which step in the REPLI-g FFPE protocol should PicoGreen quantification be done?
FAQ ID -1758
表示
How can foaming of Buffer RLT Plus lysates be avoided when using RNeasy Plus Micro and Mini Kits, or the Allprep DNA/RNA Mini Kit?
FAQ ID -1734
表示
Do you have protocols for sample processing on the Autopure LS instrument?
FAQ ID -1759
表示
Have QuantiTect Primer Assays been tested with QuantiFast SYBR Green PCR Kits on the Mastercycler ep realplex?
FAQ ID -1714
表示
Can the REPLI-g FFPE procedure restore DNA derived from FFPE tissue samples in the original order?
FAQ ID -1754
表示
Can the REPLI-g FFPE Kit also be used for formalin-fixed, ethanol preserved samples?
FAQ ID -1760
表示
Do you have a protocol for the isolation of total RNA from paraffin-embedded sections on the Biorobot M48?
FAQ ID -1733
表示
Does TopTaq Stabilizer of the TopTaq DNA Polymerase and Master Mix Kits interfere with downstream applications?
FAQ ID -1744
表示
Do you have a forensic post-PCR purification protocol to purify double-stranded DNA fragments from PCR reactions?
FAQ ID -1761
表示
Is sample pretreatment required for purifying RNA on the QIAsymphony SP?
FAQ ID -1938
表示
Is the QIAsymphony RNA Kit compatible with stabilized samples?
FAQ ID -1944
表示
Is RNA co-purified with DNA using QIAsymphony DNA Tissue protocols?
FAQ ID -1920
表示
Is there a charge for user training on the QIAsymphony SP System?
FAQ ID -1900
表示
What are the expected DNA yields from tissue processed on the QIAsymphony SP?
FAQ ID -1919
表示
QuantiTect Primer Assays are bioinformatically validated, genomewide primer sets. What does “bioinformatically validated” mean?
FAQ ID -1982
表示
What is the range of elution volumes on the QIAsymphony SP?
FAQ ID -1908
表示
How many samples can be processed per kit or per reagent cartridge for RNA purification on the QIAsymphony SP?
FAQ ID -1940
表示
How does QIAsymphony SP keep cellular samples in suspension prior to pipetting so that samples do not settle?
FAQ ID -1905
表示
How many PCR reactions can be performed for different scales of miScript Primer Assays?
FAQ ID -1990
表示
How efficient is DNA removal by a gDNA Eliminator 96 plate compared with DNase digestion on an RNeasy 96 plate?
FAQ ID -1994
表示
How long can homogenates remain on the QIAsymphony SP without risk of RNA degradation?
FAQ ID -1941
表示
How much sample can be used with the Allprep DNA/RNA 96 Kit?
FAQ ID -1997
表示
Which types and amounts of sample material can be processed for RNA extraction on the QIAsymphony SP?
FAQ ID -1937
表示
How much starting material can be used with the QIAsymphony DNA Mini Kit on the QIAsymphony SP?
FAQ ID -1917
表示
What sample types can be used with the AllPrep DNA/RNA 96 Kit?
FAQ ID -1996
表示
What sample types should be processed with the High Content (HC) protocol for DNA extraction on the QIAsymphony SP?
FAQ ID -1918
表示
What sample types can be used with the RNeasy Plus 96 Kit?
FAQ ID -1991
表示
Will mitochondrial DNA also be isolated using the DNA Tissue protocols on the QIAsymphony SP?
FAQ ID -1921
表示
Why does the Allprep DNA/RNA 96 Kit use Buffer RLT, whereas the AllPrep DNA/RNA Mini Kit uses Buffer RLT Plus?
FAQ ID -1999
表示
Why is there no vacuum-only protocol for the RNeasy Plus 96 Kit?
FAQ ID -1993
表示
What is the turn around time for custom miScript miRNA mimics, inhibitors and primer assays?
FAQ ID -1985
表示
What kind of molecules are miScript miRNA Inhibitors?
FAQ ID -1983
表示
Is it possible to modify QIAsymphony protocols?
FAQ ID -1903
表示
What are the expected yields of total RNA isolated with the QIAsymphony SP?
FAQ ID -1942
表示
What are the starting volumes of homogenate for RNA extraction on the QIAsymphony SP?
FAQ ID -1939
表示
What sample input volumes can be used on the QIAsymphony SP?
FAQ ID -1907
表示
What sample types can be processed using the tissue protocols for DNA extraction on the QIAsymphony SP?
FAQ ID -1915
表示
What kind of molecules are miScript miRNA Mimics?
FAQ ID -1986
表示
What RNA elution volumes are available with the QIAsymphony RNA Kit?
FAQ ID -1943
表示
Do limiting primer concentrations need to be determined when using QuantiFast Multiplex PCR Kits?
FAQ ID -1976
表示
Do samples require pretreatment before loading onto the QIAsymphony SP for DNA extraction?
FAQ ID -1916
表示
Can uneven sample numbers be processed on the QIAsymphony SP module?
FAQ ID -1906
表示
Does HiPerFect work for the transfection of miScript miRNA mimics and inhibitors?
FAQ ID -1984
表示
Does the QIAsymphony SP system generate run reports and/or log files?
FAQ ID -1911
表示
Do you have a protocol for the purification of archive-quality DNA from 100 to 5 x 10e8 cultured cells using Gentra Puregene Kits?
FAQ ID -1960
表示
Do you have a protocol for the purification of archive-quality DNA from 0.5–20 mg paraffin-embedded tissue using Gentra Puregene Kits?
FAQ ID -1964
表示
Do you have a protocol for the purification of archive-quality DNA from 1 ml of whole blood with the Gentra Puregene Tissue Kit?
FAQ ID -1953
表示
Do you have a protocol for rapid purification of archive-quality DNA from up to 9 x 10e6 cells using Gentra Puregene Kits?
FAQ ID -1969
表示
Can I program my own protocols for the QIAsymphony SP?
FAQ ID -1904
表示
Are QuantiFast Multiplex PCR Kits available in trial sizes?
FAQ ID -1981
表示
Can 4-plex, real-time PCR be performed on the ABI PRISM 7000, 7700, or 7900 using the QuantiFast Multiplex PCR Kit?
FAQ ID -1978
表示
Can the QIAsymphony RNA Kit be used to purify RNA from blood?
FAQ ID -1945
表示
Can the QIAsymphony SP Module be connected to a laboratory information management system (LIMS)?
FAQ ID -1909
表示
Can protocol runs on the QIAsymphony SP be interrupted and resumed?
FAQ ID -1912
表示
Can the protocols for purification of small RNAs from cells in the appendices of the RNeasy Plus 96 Handbook also be used with tissue samples?
FAQ ID -1995
表示
Do you have a protocol for the purification of archive-quality DNA from marine invertebrate tissue using Gentra Puregene Kits?
FAQ ID -1950
表示
Do you have a protocol for the purification of archive-quality DNA from nematodes using Gentra Puregene Kits?
FAQ ID -1951
表示
Do you have a protocol for the purification of archive-quality DNA from human dried blood using Gentra Puregene Kits?
FAQ ID -1959
表示
Do you have a protocol for the purification of archive-quality DNA from Gram-negative bacteria using Gentra Puregene Kits?
FAQ ID -1975
表示
Do you have a protocol for the purification of archive-quality DNA from Gram-positive bacteria using Gentra Puregene Kits?
FAQ ID -1946
表示
Do you have a protocol for the purification of archive-quality DNA from hair roots using Gentra Puregene Kits?
FAQ ID -1947
表示
Do you have a protocol for the purification of DNA from fruit flies?
FAQ ID -1970
表示
How can the QIAsymphony SP system be decontaminated?
FAQ ID -1914
表示
Do you have a protocol for the purification of archive-quality DNA from tissue fixed in ethanol or formalin using Gentra Puregene Kits?
FAQ ID -1974
表示
Do you have a protocol for the purification of archive-quality DNA from umbilical cord blood using Gentra Puregene Kits?
FAQ ID -1958
表示
Do you have a protocol for the purification of archive-quality DNA from whole blood using Gentra Puregene Kits?
FAQ ID -1954
表示
Do you have a protocol for the purification of archive-quality DNA from buffy coat using Gentra Puregene Kits?
FAQ ID -1955
表示
Do you have a protocol for the purification of archive-quality DNA from cerebrospinal fluid (CSF) using Gentra Puregene Kits?
FAQ ID -1967
表示
Do you have a protocol for the purification of archive-quality DNA from Chlamydomonas using Gentra Puregene Kits?
FAQ ID -1968
表示
Do you have a protocol for the purification of archive-quality DNA from blood smears using Gentra Puregene Kits?
FAQ ID -1948
表示
Do you have a protocol for the purification of archive-quality DNA from fecal cells using Gentra Puregene Kits?
FAQ ID -1972
表示
Do you have a protocol for the purification of archive-quality DNA from buccal brushes using Gentra Puregene Kits?
FAQ ID -1965
表示
Do you have a protocol for the purification of archive-quality DNA from fish using Gentra Puregene Kits?
FAQ ID -1973
表示
Do you have a protocol for the purification of archive-quality DNA from Eimeria oocysts using Gentra Puregene Kits?
FAQ ID -1952
表示
Do you have a protocol for the purification of archive-quality DNA from fungus using Gentra Puregene Kits?
FAQ ID -1971
表示
Do you have a protocol for cleanup of REPLI-g amplified DNA?
FAQ ID -1545
表示
What are the Tms of PCR products obtained using the miScript System?
FAQ ID -1599
表示
What is Q-Bond used in the QIAGEN Fast Cycling PCR and QuantiFast Kits?
FAQ ID -1554
表示
What controls should be used for normalizing miRNA real-time PCR data obtained with the miScript System?
FAQ ID -1596
表示
Will QuantiTect Primer Assays work at an annealing temperature of 60ºC with QuantiFast SYBR Green PCR and RT-PCR Kits?
FAQ ID -1553
表示
Which homogenization method do you recommend for tissues stored in Allprotect Tissue Reagent?
FAQ ID -1572
表示
Can different incubation times be used for the 2 hour amplification step in the QuantiTect Whole Transcriptome protocol?
-8
表示
Does residual Allprotect Tissue Reagent left behind on tissue samples interfere with DNA, RNA, and protein purification?
FAQ ID -1573
表示
Is cDNA generated with the QuantiTect Whole Transcriptome Kit suitable for use in microarray analysis?
FAQ ID -1587
表示
Do you have a protocol for purification of genomic DNA from cultured cells using the QIAamp DNA Micro Kit?
FAQ ID -1547
表示
Do you have a protocol for concentration of RNA in 96-well plates?
FAQ ID -1546
表示
Do you have a protocol for purification of total RNA from fatty tissues using QIAzol Lysis Reagent and MaXtract High Density?
FAQ ID -1550
表示
Which real-time PCR kits are recommended downstream of the QuantiTect Whole Transcriptome Kit?
FAQ ID -1592
表示
What primers are used in the reverse-transcription step of the QuantiTect Whole Transcriptome procedure?
FAQ ID -1584
表示
Can the AllPrep DNA/RNA/Protein Mini Kit be used with fibrous or lipid tissues?
FAQ ID -1579
表示
What is the maximum amount of RNA that can be used for amplification with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1591
表示
What starting amount of RNA purified using an miRNeasy Kit should be used with the miScript System?
FAQ ID -1597
表示
Can RNA purified from formalin-fixed, paraffin-embedded (FFPE) tissue be used with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1583
表示
Can samples in Allprotect Tissue Reagent undergo repeated freeze-thaws without degradation of DNA, RNA, and protein?
FAQ ID -1575
表示
Can the QuantiFast Probe PCR +ROX Vial Kit be used on the ABI PRISM 7900 and Applied Biosystems 7500 cyclers?
FAQ ID -1555
表示
Does Buffer APP in the AllPrep DNA/RNA/Protein Mini Kit contain acetone?
FAQ ID -1576
表示
Does cDNA amplified with the QuantiTect Whole Transcriptome Kit correspond to full-length RNA transcripts?
FAQ ID -1585
表示
Can tissue incubated in Allprotect Tissue Reagent be used for morphological studies?
FAQ ID -1571
表示
Can less than 10 ng RNA be used with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1590
表示
Can cDNA prepared by any method be used as starting material in the ligation reaction of the QuantiTect Whole Transcriptome Kit?
FAQ ID -1589
表示
Can Allprotect Tissue Reagent be used to stabilize RNA, DNA and proteins in cells, bacteria, yeast, and plants?
FAQ ID -1574
表示
Can degraded RNA be used with the QuantiTect Whole Transcriptome Kit?
FAQ ID -1586
表示
How much cDNA is sufficient for real-time PCR detection of miRNA transcripts generated with the miScript System?
FAQ ID -1598
表示
How many samples can be run in parallel with the Rotor-Gene Q real-time PCR instrument?
FAQ ID -1519
表示
What main input voltage is required for the QIAxcel Analyzer?
FAQ ID -1821
表示
Is there a quality difference between CompactPrep Plasmid Mega and Giga and the CompactPrep Plasmid Midi and Maxi Kits?
FAQ ID -1882
表示
The Gel Cartridge is installed and all status indicators for the QIAxcel System are good but when clicking the "RUN" button, nothing happens. The green highlight goes down the Sequence?
FAQ ID -1850
表示
Why does the copy function not apply relative to migration time and normalized area values after loading the DNA size marker table and adding the alignment marker peaks on the QIAxcel System?
FAQ ID -1832
表示
Can customers use their own DNA size marker with the QIAxcel System and if yes, what concentration should be used?
FAQ ID -1841
表示
Can data be saved at once with the QIAxcel System after analysis of all samples in a 96-well PCR plate?
FAQ ID -1861
表示
How can a positive threshold be set when running the QIAxcel System?
FAQ ID -1843
表示
How long will the intensity calibration procedure on the QIAxcel System take?
FAQ ID -1826
表示
Will the QIAxcel System run using a green Data Review Software Key?
FAQ ID -1853
表示
When should an intensity calibration be re-performed on the QIAxcel System?
FAQ ID -1825
表示
Can the QIAxcel System or QIAxcel Advanced be connected to a network?
FAQ ID -1862
表示
How can a clogged capillary channel be identified when running samples on the QIAxcel System or QIAxcel Advanced?
FAQ ID -1836
表示
Can the QIAxcel software be loaded to another PC to view the data generated with the QIAxcel System?
FAQ ID -1855
表示
Can multiple QIAxcel Systems be run from one computer?
FAQ ID -1860
表示
How often should the solutions in the Buffer Tray for the QIAxcel System or QIAxcel Advanced be replaced?
FAQ ID -1840
表示
How often should the alignment marker for the QIAxcel System be changed?
FAQ ID -1839
表示
If the M500 method is used with the QIAxcel System, does a new DNA reference marker table have to be created?
FAQ ID -1856
表示
In the results table generated with the QIAxcel System, what does "normalized area" mean?
FAQ ID -1854
表示
What is the composition of buffer OCD?
FAQ ID -423
表示
What is the composition of buffer QN?
FAQ ID -414
表示
What is the composition of buffer OCL?
FAQ ID -422
表示
What is the composition of buffer OL2?
FAQ ID -424
表示
Can the QIAamp MinElute Virus Kits be used to extract viral nucleic acid from cell culture supernatant?
FAQ ID -472
表示
Can RNAi experiments be performed in Drosophila?
FAQ ID -436
表示
How is the RNeasy Lipid Tissue Mini Kit different from the RNeasy Mini Kit?
FAQ ID -468
表示
Has RNAi been successful using siRNA in Zebrafish and Xenopus?
FAQ ID -400
表示
Are Northern Blots sensitive enough to detect siRNA-induced gene silencing?
FAQ ID -403
表示
Can I use the RNeasy MinElute Cleanup Kit to clean up my in vitro transcription reaction?
FAQ ID -429
表示
What is the composition of buffer OEB?
FAQ ID -420
表示
Why is the pQE DNA provided in QIAexpress Kits blue in color?
FAQ ID -487
表示
What is the minimum elution volume when using the RNeasy Micro Kit?
FAQ ID -428
表示
What is the maximum amount of starting material that can be processed with the RNeasy Micro Kit?
FAQ ID -426
表示
What is the minimum elution volume when using the RNeasy MinElute Cleanup Kit?
FAQ ID -432
表示
What is the smallest sample size that can be used with RNeasy Mini Kits?
FAQ ID -485
表示
What is a homogeneous LiquiChip assay?
FAQ ID -476
表示
What detection reagents (reporter fluorophores) do you recommend for the LiquiChip System?
FAQ ID -480
表示
What are the excitation and emission wavelengths of the reporter and classification lasers of the LiquiChip Instrument?
FAQ ID -479
表示
What is the binding capacity of the RNeasy MinElute Cleanup Kit column?
FAQ ID -430
表示
What is the composition and size of the LiquiChip Beads?
FAQ ID -475
表示
What is the binding capacity of the RNeasy Micro Kit column?
FAQ ID -427
表示
Is dihydrofolate reductase (DHFR) immunogenic?
FAQ ID -471
表示
What are some of the assays that are adaptable to the LiquiChip System?
FAQ ID -477
表示
My QuantiTect Master Mix did not freeze at degrees. Is it still ok to use?
-20
表示
I want to start with gene silencing (RNAi) experiments. Do you have informational literature?
FAQ ID -580
表示
Is it possible to use less than 1 mg of protein with the PhosphoProtein Purification Kit?
FAQ ID -599
表示
Is it possible to use a QIAzol lysate for the isolation of RNA from tissue on the BioRobot EZ1?
FAQ ID -573
表示
What is a quenched FRET assay?
FAQ ID -542
表示
What do you recommend for isolating RNA from more than 100 mg of plant tissue?
FAQ ID -570
表示
What happens if I spin my lysate on the RNeasy Spin Columns at maximum speed?
FAQ ID -514
表示
How should I dissolve the lyophilized Anti-His and Tag Antibodies?
-100
表示
Is it possible to perform a UNG treatment when using QuantiTect kits?
FAQ ID -564
表示
Is it possible to clean up a methylation reaction containing bisulfite with QIAquick Cleanup Kits?
FAQ ID -519
表示
Is it possible to isolate both RNA and recombinant 6xHis-tagged protein from the same sample?
FAQ ID -532
表示
Why are my realtime PCR amplification plots hook-shaped?
FAQ ID -587
表示
Why are samples centrifuged at 4°C after the addition of chloroform when using RNeasy Lipid Tissue Kits?
FAQ ID -533
表示
How was it determined that the PhosphoSerine Antibody will bind phosphoserines only?
FAQ ID -579
表示
If pQE40 is used to express a fusion protein with DHFR, can the DHFR be cleaved afterwards?
FAQ ID -513
表示
Which chloroform should I use for the RNeasy Lipid Tissue Kit?
FAQ ID -516
表示
Will pancreas tissue swim on top of RNAprotect Tissue Reagent?
FAQ ID -536
表示
Will the 2x QIAGEN Multiplex PCR Master Mix freeze at -20°C?
FAQ ID - 525
表示
Why does my realtime PCR assay quality decrease over time?
FAQ ID -589
表示
What is the longest fragment that was cloned with the pQE UA Cloning Vector?
-30
表示
What is the difference between BSA-free and BSA-containing RGS-His Antibody?
FAQ ID -569
表示
When using QIAzol Lysis Reagent for RNA extraction, I see a pinkish colored aqueous phase! Is it OK?
FAQ ID -534
表示
Where can I find the public Smith-Waterman homology search tool that you refer to on your siRNA online design page?
FAQ ID -562
表示
What reaction volume should I use with QuantiTect Kits?
FAQ ID -551
表示
What makes QIAGEN's 10x Taq and HotStarTaq DNA Polymerase PCR buffer superior?
FAQ ID -566
表示
How many template copies can I detect using QuantiTect Kits in real-time PCR?
FAQ ID -543
表示
Can I use RNAiFect for co-transfection of plasmid DNA and siRNA?
FAQ ID -515
表示
Does DEPC harm RNA?
FAQ ID -529
表示
Does endogenously expressed DAPase in human cells degrade proteins that are expressed in cell culture?
FAQ ID -527
表示
Can the MAPK1 control siRNA be used for rat cells?
FAQ ID -547
表示
Are the columns of the MinElute Reaction Cleanup-, Gel Extraction-, and PCR Purification Kit identical?
FAQ ID -581
表示
After using your U/A PCR Cloning Kit I can detect colonies, which are light blue, and not really white. Why is that?
FAQ ID -512
表示
Can I make a master mix with QuantiProbes, primers, and all other reaction components and store it for later use?
FAQ ID -584
表示
Can I homogenize samples in QIAzol using the QIAshredder?
FAQ ID -501
表示
Can I shorten the activation time for the HotStarTaq DNA Polymerase?
FAQ ID -565
表示
Does QIAGEN sell 6xHis-tagged proteins besides the 6xHis Protein Ladder?
FAQ ID -594
表示
Do you offer QIAshredder spin columns for the RNeasy Midi/Maxi Kit format? If not, what is the alternative?
FAQ ID -560
表示
Do you provide control proteins for use with the PhosphoProtein Purification Kit?
FAQ ID -596
表示
How long should the amplicon be if I am using QuantiTect SYBR Green detection?
FAQ ID -553
表示
How is an antibody epitope determined?
FAQ ID -593
表示
Do I need to calibrate my real-time cycler if I want to use Yakima Yellow?
FAQ ID -540
表示
Do we recommend pooling siRNA sequences?
FAQ ID -517
表示
Does the His-tag interfere with the purification procedure of the QIAGEN PhosphoProtein Purification Kit?
FAQ ID -598
表示
Does the use of MAPK1 as a control in siRNA transfection experiments have secondary effects on the cell culture?
FAQ ID -548
表示
Do you have a protocol to isolate RNA from blood and bone marrow using the BioRobot EZ1?
FAQ ID -567
表示
Do you have any recommendations for using the PosphoProtein Kit with starting material other than cells?
FAQ ID -597
表示
Do you have a protocol for isolating RNA from yeast using RNeasy?
FAQ ID -535
表示
What is the run time for the BioSprint 96 DNA Blood protocol on the BioSprint 96 instrument?
FAQ ID -622
表示
Will REPLI-g work at high temperatures?
FAQ ID -656
表示
The Multiflow Dispense Head on my BioRobot is not dispensing the correct amount of liquid. What can I do?
FAQ ID -652
表示
What is the smallest amount of DNA I can put into a 50 ul REPLI-g reaction?
FAQ ID -663
表示
What is the recommended incubation time to stabilize tissue RNA in RNAprotect Tissue Reagent?
FAQ ID -647
表示
What do you mean by “Quantification of locus representation” in REPLI-g WGA product?
FAQ ID -698
表示
What is REPLI-g whole genome amplification?
FAQ ID -654
表示
What is the average amount of DNA and RNA present in 1 ml normal serum?
FAQ ID -635
表示
What is the biggest protein that can be synthesized with the EasyXpress Protein Synthesis System?
FAQ ID -601
表示
What is the length of the MDA whole genome amplification product?
FAQ ID -690
表示
What is the expected yield of genomic DNA isolated from bacteria with the DNeasy Blood & Tissue or QIAamp DNA Mini Kit?
FAQ ID -632
表示
Is it possible to perform laser microdissection with tissues stabilized with RNAprotect Tissue reagent?
FAQ ID -608
表示
Is it possible to synthesize membrane proteins using the EasyXpress Protein Synthesis Kit?
FAQ ID -602
表示
What are Elution Microtube adapters and Microplate adapters used in the DirectPrep 96 Miniprep Kit, and how can I order them?
FAQ ID -646
表示
What are the advantages of REPLI-g over conventional DNA sample processing and amplification methods?
FAQ ID -686
表示
Why do I get amplification in a negative control DNA tube using the REPLI-g Kit for WGA?
FAQ ID -675
表示
Why did you choose MAPK1 as a positive control in the QIAGEN RNAi Human/Mouse Control Kit?
FAQ ID -604
表示
Will the PhosphoSerine antibody recognize Serine residues if the neighboring residues are Leucine or Isoleucine?
FAQ ID -644
表示
Will TA cloning work with REPLI-g WGA product?
FAQ ID -672
表示
Will DNA from chromosomes collected in TE with a drop of mineral oil work with REPLI-g amplification?
FAQ ID -664
表示
What is the stability of the REPLI-g MDA product?
FAQ ID -693
表示
When delivering liquid to a 96-well plate using the MultiFlow Dispenser Head on my BioRobot , one or more rows in the plate contains less liquid per well than specified by the protocol. What is going wrong?
FAQ ID -653
表示
Where should I add a dye-label modification on the siRNA?
FAQ ID -648
表示
What types of materials from environmental samples could interfere with WGA?
FAQ ID -666
表示
Can I stabilize RNA in bacteria grown on solid media or substrate using the RNAprotect Bacteria Reagent?
FAQ ID -615
表示
Can I re-amplify whole genome amplification product?
FAQ ID -670
表示
Can I use another lysis buffer than the one supplied in the PhophoProtein Purification Kit?
FAQ ID -645
表示
Can I run less than 15 samples on the BioSprint 15 instrument?
FAQ ID -621
表示
Can the QIAshredder Maxi Spin Columns from the DNeasy Plant Maxi Kit be used for RNeasy samples?
FAQ ID -616
表示
Do you have an off-the shelf diagnostics kit for WGA?
FAQ ID -678
表示
Are there components in biological samples that can inhibit the REPLI-g reaction?
FAQ ID -667
表示
Are the BioSprint 15/96 instruments stand-alone workstations?
FAQ ID -620
表示
Can the computer for the LiquiChip Workstation be networked?
FAQ ID -629
表示
Are QIAGEN EZ Competent Cells of the QIAGEN PCR Cloning Kit dam+ or dam-?
FAQ ID -638
表示
Are samples that are contaminated with high molecular weight DNA (e.g. from a paramedic or police officer) a problem with REPLI-g amplification?
FAQ ID -683
表示
Can BAC DNA prepared with the R.E.A.L. Prep 96 Plasmid Kit be used for high-throughput sequencing?
FAQ ID -643
表示
Can I do whole genome amplification from brain tissue using REPLI-g?
FAQ ID -669
表示
Can I do whole genome amplification from mitochondrial DNA using REPLI-g?
FAQ ID -668
表示
Can FTA paper for dried blood spots be used with REPLI-g?
FAQ ID -685
表示
How can I quantify the amount of REPLI-g DNA I have amplified?
FAQ ID -694
表示
Can I amplify from plasma or serum samples using the REPLI-g Mini/Midi kits?
FAQ ID -671
表示
How should I store the REPLI-g amplification product?
FAQ ID -692
表示
Is 2 kb the minimal gDNA fragment size for REPLI-g Whole Genome Amplification?
FAQ ID -682
表示
How long can I store bacterial culture stabilized in RNAprotect Bacteria Reagent?
FAQ ID -614
表示
Do I need to clean up the REPLI-g amplification product for downstream analysis?
FAQ ID -691
表示
Do you have a kit for RNA isolation from any kind of sample type?
FAQ ID -627
表示
Does REPLI-g technology for whole genome amplification work with paraffin embedded samples?
FAQ ID -673
表示
How can I determine the quality of my REPLI-g amplified products?
FAQ ID -695
表示
How can I decrease ribosomal RNA (rRNA) contamination using Oligotex?
FAQ ID -642
表示
Do you know of anything in the buffers/DNA sample that can cause bias in REPLI-g WGA?
FAQ ID -684
表示
Do you have a protocol for the purification of DNA from rodent tail using the BioSprint System?
FAQ ID -979
表示
Do you have a protocol for the isolation of DNA from epithelial cells mixed with sperm cells?
FAQ ID -926
表示
Do you have a protocol for isolation of genomic DNA from saliva using the DNeasy Blood & Tissue Kit?
FAQ ID -931
表示
Do you have a protocol for purification of DNA from clotted blood using the FlexiGene DNA Kit?
FAQ ID -973
表示
Do you have a protocol for Streptokinase treatment of clotted blood?
FAQ ID -912
表示
Do you have a protocol for the isolation of total nucleic acids from animal and human cells on the BioRobot EZ1?
FAQ ID -974
表示
Do you have a protocol for the isolation of total RNA from plant tissue using QIAGEN-tips?
FAQ ID -949
表示
Do you have a protocol for the isolation of total RNA from buccal swabs?
FAQ ID -956
表示
Do you have a protocol for the isolation of viral DNA from stool?
FAQ ID -929
表示
Do you have a protocol for the isolation of total RNA from plants using the RNeasy 96 Kit?
FAQ ID -951
表示
Do you have a protocol for the isolation of DNA from formalin-preserved stool samples?
FAQ ID -922
表示
Do you have a protocol for the isolation of genomic DNA from fungi?
FAQ ID -911
表示
Do you have a protocol for the isolation of genomic DNA and/or proteins from fatty tissue treated with QIAzol?
FAQ ID -955
表示
Do you have a protocol for the purification of DNA from cells using the BioSprint System?
FAQ ID -977
表示
Do you have a protocol for the purification of DNA from dried blood spots using the BioSprint System?
FAQ ID -982
表示
Do you have a protocol for the preparation of tissues preserved in RNAprotect Tissue Reagent for pathological studies?
FAQ ID -950
表示
Do you have a protocol for the purification of DNA from buccal swabs using the BioSprint System?
FAQ ID -983
表示
Do you have a protocol for isolation of genomic and viral DNA from lymphocytes using QIAGEN Genomic-tips?
FAQ ID -901
表示
Do you have a protocol for isolation of genomic and plasmid DNA from cell cultures using QIAGEN Genomic-tips?
FAQ ID -902
表示
Do you have a protocol for transfection of adherent cells with low concentrations of siRNA using RNAiFect Transfection Reagent?
FAQ ID -970
表示
Do you have a protocol for GMO testing of food samples?
FAQ ID -921
表示
Do you have a protocol for isolation of bacterial DNA from soil?
FAQ ID -923
表示
Do you have a protocol for isolation of genomic DNA from dried blood spots using the QIAamp 96 DNA Blood Kit?
FAQ ID -919
表示
Do you have a protocol for isolation of genomic DNA from insects?
FAQ ID -904
表示
Do you have a protocol for detection of HBV DNA by PCR?
FAQ ID -915
表示
Does QIAGEN sell a vector with a T7 promotor for use with the EasyXpress Protein Synthesis Insect Kit?
FAQ ID -937
表示
Can the BioSprint instruments be placed in a cool room?
FAQ ID -938
表示
Do you have a protocol for Acetyl Cysteine (NALC) treatment of viscous samples?
FAQ ID -913
表示
Do you have a protocol for co-transfection of adherent cells with siRNA and plasmid DNA?
FAQ ID -969
表示
Do you have a protocol for adding new reporter dyes to the ABI PRISM 7900 Sequence Detection System?
FAQ ID -965
表示
Do you have a protocol for cleanup of non-radioactive DNA samples?
FAQ ID -945
表示
Do you have a protocol for radioactive labelling of cDNA?
FAQ ID -960
表示
Do you have protocols for multiple extractions of DNA fragments from agarose gels?
FAQ ID -944
表示
Why is it not recommended to stabilize cells with RNAprotect Tissue Reagent?
FAQ ID -941
表示
Do you have a protocol for the detection of Bordetella pertussis DNA by PCR?
FAQ ID -914
表示
Do you have a protocol for the isolation of DNA from cultured cells using the BioRobot EZ1?
FAQ ID -990
表示
Do you have a protocol for performing quantitative multiplex PCR on the LightCycler 2.0 system?
FAQ ID -966
表示
Do you have a protocol for long-term, siRNA-mediated gene silencing using HiPerFect Transfection Reagent?
FAQ ID -972
表示
Do you have a protocol for manual purification of 6xHis-tagged proteins expressed in E. coli using Ni-NTA Superflow?
FAQ ID -967
表示
Do you have a protocol for purification of DNA from cultured animal cells using the DNeasy 96 Blood & Tissue Kit?
FAQ ID -934
表示
Do you have a protocol for purifying 2x96 PCR samples simultaneously with the QIAquick 96 PCR Purification Kit?
FAQ ID -935
表示
Do you have a protocol for purification of DNA fragments from Cy3/Cy5 dye-label reactions?
FAQ ID -947
表示
Do you have a protocol for polyacrylamide gel analysis of oligonucleotides?
FAQ ID -961
表示
Do you have a protocol for isolation of genomic DNA from plants and filamentous fungi using QIAGEN Genomic-tips?
FAQ ID -905
表示
Do you have a protocol for isolation of genomic DNA from flies using QIAGEN Genomic-tips?
FAQ ID -903
表示
What are exo-resistant random hexamers used in the REPLI-g reaction?
FAQ ID -710
表示
The Sigma Centrifuge makes a loud noise at low speeds which disappears at higher speeds, when using the 2x96-well plate rotor. What is the problem?
FAQ ID -776
表示
Is RNAprotect Bacteria Reagent compatible with the RNeasy Mini Kit?
FAQ ID -797
表示
What is the basic technology behind the Strep-tag Protein Purification System?
FAQ ID -740
表示
What are the expected average DNA yields from plant extractions on the BioSprint 96?
FAQ ID -771
表示
If template abundance differs significantly between housekeeping and target gene, are both amplified equally efficient with the QuantiTect Multiplex Kits?
FAQ ID -718
表示
How to quantitate DNA purified using the BioSprint 96?
FAQ ID -773
表示
How to store DNA from forensic samples eluted into water on the EZ1 biorobot in TE buffer instead?
FAQ ID -734
表示
Is it possible to use LiquiChip beads for FACS applications?
FAQ ID -733
表示
Is it possible to buy the EZ Competent Cells of the QIAGEN PCR Cloning Plus Kit separately?
FAQ ID -763
表示
Is GFP excited and detected by the green laser of the LiquiChip System?
FAQ ID -737
表示
Which Qproteome or Protein Fractionation Kits from QIAGEN are compatible with tissue samples?
FAQ ID -755
表示
Why are some of my RNAprotect-stabilized samples frozen at 0ºC while others are not?
FAQ ID -758
表示
Why are the QuantiTect and QuantiFast Multiplex PCR Kits limited to triplex real-time PCR on some cyclers?
FAQ ID -715
表示
Why should DNA or cDNA targets be less than 250 bp long for real-time PCR?
FAQ ID-751
表示
Where can I find info on compatible reporter dyes for use in real-time multiplex PCR using the QuantiTect Multiplex PCR Kits?
FAQ ID -719
表示
Why might my gene of interest drop out during WGA if it is not near a telomere or centromere?
FAQ ID -703
表示
Will the random hexamers in the REPLI-g reaction interfere with downstream analysis?
FAQ ID -713
表示
Why is there no detection of free reporter fluorescence in the LiquiChip System?
FAQ ID -732
表示
What is the cell number range one can use with the FastLane Cell cDNA Kit for real-time RT-PCR?
FAQ ID -782
表示
What negative (unphosphorylated) and positive (phosphorylated) control proteins do you recommend for use with the PhosphoProtein Purification Kit?
FAQ ID -779
表示
What is the enzyme used in the REPLI-g reaction?
FAQ ID -704
表示
What type of Sequencing Services does QIAGEN offer?
FAQ ID -781
表示
Where can I find a copy of the report files generated by running accessory protocols "Dilutor Delivery (monthly)" and "High-Speed Pipetting Sytem (monthly)" on my BioRobot 9604?
FAQ ID -766
表示
What is the general sensitivity level of the LiquiChip System?
FAQ ID -731
表示
Can QIAGEN's Taq- and HotstarTaq DNA Polymerases be used for cycle sequencing?
FAQ ID -741
表示
Can I use the PhosphoProtein Purification Kit to purify phosphorylated peptides of around 1 kD size?
FAQ ID -778
表示
Can RNAprotect Tissue Reagent be used to stabilize tissue which has already been flash-frozen?
FAQ ID -757
表示
Can lyophilized plant material be used for DNA extraction on the BioSprint 96?
FAQ ID -772
表示
Can the REPLI-g WGA enzyme work with labeled dNTPs?
FAQ ID -706
表示
Does the QIAamp DSP Virus Kit require the QIAvac 24 Plus, or can I use it with my own laboratory vacuum system?
FAQ ID -789
表示
Can the MAPK1 siRNA of the RNAi Human/Mouse Starter Kit be purchased separately?
FAQ ID -744
表示
Can the QIAvac 96 vacuum manifold be used with DirectPrep 96 plates?
FAQ ID -722
表示
Are the buffers in the Ni-NTA Fast Start Kit the same as the ones for use with Ni-NTA purchased separately?
FAQ ID -791
表示
Any data on the fidelity of the REPLI-g MDA technique?
FAQ ID -707
表示
Are Centromeres and Telomeres amplified using REPLI-g WGA?
FAQ ID -702
表示
Can I use my own primers for REPLI-g WGA to amplify a specific chromosomal region?
FAQ ID -712
表示
Can I do 4-plex real-time PCR, on the ABI PRISM 7000, 7700, or 7900 using the QuantiTect Multiplex PCR Kit?
FAQ ID -716
表示
How can one perform multiplex real-time PCR analysis using the LightCycler 2.0?
FAQ ID -780
表示
How can I be sure that I am harvesting my induced bacterial culture at the best time point for protein expression?
FAQ ID -788
表示
How do the FastLane Cell cDNA Kit and QuantiTect Reverse Transcription Kit eliminate genomic DNA contamination?
FAQ ID -783
表示
How many cells can be used with the FastLane Cell cDNA Kit?
FAQ ID -796
表示
Do you have an antibody for Western Blot Analysis of MAPK1 gene knockdown using your MAPK1 control siRNA?
FAQ ID -746
表示
Can frozen blood be used for whole genome amplification with REPLI-g?
FAQ ID -794
表示
Do I have to switch off the laser of the LiquiChip Workstation overnight?
FAQ ID -736
表示
How many reporter dyes can be used in the same analysis using the LiquiChip Workstation?
FAQ ID -738
表示
Do I need to determine limiting primer concentrations with the QuantiTect Multiplex PCR Kits?
FAQ ID -714
表示
Do you synthesize thiophosphate modified random hexamers?
FAQ ID -711
表示
Has anyone verified whole genome amplification accuracy with Sequencing?
FAQ ID -701
表示
Do you have a protocol for the fixation of cells transfected with fluorescently labeled siRNA?
FAQ ID -793
表示
How best to handle the light sensitive LiquiChip reagents?
FAQ ID -735
表示
Do you have information on the use of recombinant DNA and RNA as absolute standards for realtime RT-PCR?
FAQ ID -729
表示
Is it possible to transfect DNA into insect cell lines such as Drosophila melanogaster S2?
FAQ ID -397
表示
Is it possible to isolate free genomic DNA using the QIAamp UltraSens Virus Kit?
FAQ ID -358
表示
Is it possible to store TAGzyme enzymes at°C?
-80
表示
I accidentally added RNAprotect Tissue Reagent to my cells, and now the cells are difficult to pellet. What can I do?
FAQ ID -364
表示
What are the calculated molecular weights of the TAGZyme enzymes?
FAQ ID -329
表示
How complete is the removal of DAPase in the TAGZyme process?
FAQ ID -319
表示
How long is fluorescence detectable in cells after transfection with fluorescently labeled siRNAs?
FAQ ID -392
表示
How do I submit a siRNA order by telephone or online?
FAQ ID -399
表示
How many transfections can I perform with 20 nmol of HPP grade siRNA?
FAQ ID -367
表示
Which primers can I use for sequencing pQE-expression vector constructs?
FAQ ID -343
表示
What is the standard assay volume recommended for LiquiChip assays?
FAQ ID -330
表示
What is the acceptable maximum g force for centrifugation of Xa Removal Resin?
FAQ ID -320
表示
What is the lowest elution volume that can be used with QIAprecipitator Midi and Maxi Modules?
FAQ ID -307
表示
What is the composition of Buffer FG3?
FAQ ID -356
表示
Can I use ethanol instead of isopropanol for DNA precipitation when using HiSpeed Plasmid Kits?
FAQ ID -354
表示
303 - Can I use my own lysis buffer with the DNeasy Blood & Tissue or QIAamp DNA Mini Kit?
表示
Can I use a partial MinElute 96 UF plate?
FAQ ID -355
表示
Can I use the RNeasy Mini Kit or RNeasy 96 Kit with fewer than 100 cells?
FAQ ID -372
表示
Can I use water for elution from the QIAprecipitator of the HiSpeed Plasmid Kits?
FAQ ID -306
表示
Are the QIAprecipitator Midi and Maxi Modules of the HiSpeed Plasmid Kits interchangeable?
FAQ ID -308
表示
Apart from the antibody itself, does the Penta-His Biotin Conjugate solution contain any protein?
FAQ ID -359
表示
Are QIAGEN monoclonal Anti His Antibodies glycosylated?
FAQ ID -334
表示
Can I perform in-vitro transcription with the pDrive Cloning Vector from the QIAGEN PCR Cloning Kit?
FAQ ID -332
表示
Do the QuantiTect SYBR Green Kits contain a stabilization reagent that inhibits the sensitivity of real-time PCR?
FAQ ID -328
表示
Do I need to anneal, deprotect or desalt my QIAGEN siRNA?
FAQ ID -398
表示
How are siRNAs introduced into C. elegans?
FAQ ID -396
表示
Do pQE vectors contain the CAT gene?
FAQ ID -362
表示
How can I improve the expression of proteins containing hydrophobic regions?
FAQ ID -339
表示
How can I check if any residual proteins remain on the Ni-NTA Agarose matrix after elution?
FAQ ID -324
表示
Do freeze-thaw cycles affect the stability of the U-overhang on the pDrive Cloning Vector?
FAQ ID -323
表示
Can RNAprotect Tissue Reagent be used to store previously isolated RNA?
FAQ ID -337
表示
Can MinElute 96 UF PCR be used to purify PCR samples which contain mineral oil?
FAQ ID -360
表示
Does SYBR Green dye present in QuantiTect kits interfere with ethidium bromide staining?
FAQ ID -312
表示
Do any of the buffers in the HotStarTaq DNA Polymerase Kit contain Triton?
FAQ ID -327
表示
Do any of the kit components or the product packaging of the QIAamp 96 DNA Blood Kit contain latex?
FAQ ID -318
表示
What data documentation does QIAGEN's Sequencing Service provide for customers?
FAQ ID -832
表示
What are the sequences of the FlexiTube siRNAs?
FAQ ID -851
表示
My BioRobot 9604 came with several Accessory Applications. Is it recommended I run these protocols?
FAQ ID -872
表示
What is the proper way to turn on or turn off the EZ1 instrument?
FAQ ID -870
表示
What is the Energy Mix in the EasyXpress Kits?
FAQ ID -846
表示
What is the concentration of the primers in a reaction using the QuantiTect Primer Assays?
FAQ ID -850
表示
I would like to sequence my siRNA constructs. Does QIAGEN offer Sequencing Services for cloned siRNA?
FAQ ID -829
表示
Is it possible to use frozen cell pellets with the FastLane Cell cDNA Kit?
FAQ ID -835
表示
Is it possible to elute plasmid DNA from the QIAprep Spin Miniprep columns with buffer containing Potassium Phosphate?
FAQ ID -854
表示
Is it possible to perform immunoprecipitation (IP) directly on protein fractions from the Qproteome Cell Compartment Kit?
FAQ ID -855
表示
Is it possible to adjust the Lysis Buffer volume used with the Qproteome Bacterial Protein Preparation Kit?
FAQ ID -841
表示
Is it possible to use QIAGEN's pQE-TriSystem Vectors with the EasyXpress Protein Synthesis Insect Kit?
FAQ ID -876
表示
Is there a stopping point in the protocol for Suspended Cells using the FastLane Cell cDNA Kit?
FAQ ID -837
表示
Is the random biotin labeling of proteins expressed with your EasyXpress Biotin Labeling Kit as sensitive as labeling with radioactivity?
FAQ ID -875
表示
Will biotin detection assays be efficient when doing in vitro translation from E. coli lysates with the EasyXpress Site-Specific Biotin Kit?
FAQ ID -878
表示
Why would clumps occur following the addition of Buffer P2 when using LyseBlue Reagent in a plasmid preparation?
FAQ ID -862
表示
Will acetone precipitation recommended in the Qproteome Protocols denature Protein?
FAQ ID -807
表示
Will site-specific biotin labeling with the EasyXpress Site-Specific Biotin kit alter the structure and function of my protein?
FAQ ID -877
表示
Will the sequences of the QuantiTect Primer Assays be provided?
FAQ ID -804
表示
Will the FastLane Cell cDNA Kit work with suspension cells?
FAQ ID -801
表示
Which resin is used in the QIAexpress Ni-NTA Fast Start Columns?
FAQ ID -836
表示
What publicly funded Genome Sequencing Projects has QIAGEN's Sequencing Service been involved in?
FAQ ID -815
表示
What is the typical yield of site-specific labeled protein generated using the EasyXpress Site-Specific Biotin Kit?
FAQ ID -873
表示
What programs does your Sequencing Service use to ensure accurate base calling, Sequence Quality, and Alignment?
FAQ ID -831
表示
Where can I find a copy of the report file generated by running 'Maintenance Protocol I' on my BioRobot MDx?
FAQ ID -806
表示
Which fraction will contain soluble mitochondrial proteins using the Qproteome Cell Compartment Kit?
FAQ ID -839
表示
Which fraction will contain endosomal, microsomal and lysosomal proteins using the Qproteome Cell Compartment Kit?
FAQ ID -808
表示
Where can I find QIAGEN products for a specific gene or gene product?
FAQ ID -803
表示
Can the QuantiTect Primer Assays be used for detection of genomic DNA?
FAQ ID -811
表示
Do I need to use RNase inhibitors with the RNeasy Kits?
FAQ ID -813
表示
Do the Buffers CE1 - CE4 of the Qproteome Cell Compartment Kit contain DTT or any reducing agent?
FAQ ID -824
表示
Can the FastLane Cell cDNA Kit also be used for qualitative end-point PCR?
FAQ ID -834
表示
Can the FastLane Cell cDNA Kit be used with tissue?
FAQ ID -821
表示
Do you have a protocol for the isolation of bacteriophage P1 derived constructs with any of your plasmid kits?
FAQ ID -883
表示
Do you have a protocol for the isolation of BAC DNA using the QIAGEN Plasmid Midi Kit?
FAQ ID -881
表示
895 - Do you have a protocol for the isolation of endotoxin-free plasmid DNA using the QIAGEN Plasmid Midi Kit?
表示
Do you have a protocol for isolation of plasmid DNA using the Sigma Centrifuge 4?
-15
表示
Can Buffer R1 of the R.E.A.L. Prep 96 Plasmid Kit be replaced with Buffer P1?
FAQ ID -823
表示
Are there specific recommendations for performing RT-PCR on RNA isolated from paraffin-embedded samples?
FAQ ID -828
表示
Can I stabilize adipose tissue using RNAprotect Tissue Reagent prior to RNA isolation?
FAQ ID -856
表示
Can I use the PhosphoProtein Purification Kit for the isolation of phosphorylated proteins from yeast?
FAQ ID -838
表示
Can I use QIAGEN's pQE vectors as templates in the EasyXpress Biotin Labeling Kits?
FAQ ID -874
表示
Can I use my gene-specific primers with the FastLane Cell cDNA Kit and the QuantiTect Reverse Transcription Kit?
FAQ ID -812
表示
Can I use LyseBlue with R.E.A.L. Prep 96, QIAwell Ultra, or QIAprep 96 Turbo Miniprep Kits for the BioRobot systems?
FAQ ID -863
表示
Do you have information on in vivo RNA interference experiments?
FAQ ID -817
表示
Do you sell the ATP-Dependent Exonuclease of the QIAGEN Large-Construct Kit separately?
FAQ ID -825
表示
I cannot see the LCD display fonts on the Sigma Centrifuge. How do I adjust the contrast?
FAQ ID -822
表示
How long does a typical in vitro translation reaction take with your large-scale EasyXpress protein synthesis kits?
FAQ ID -880
表示
How much protein can be produced with the EasyXpress Protein Synthesis Mega Kit?
FAQ ID -843
表示
Do you have a protocol for the isolation of very low-copy plasmids from Streptomyces spp.?
FAQ ID -893
表示
Do you have a protocol for the isolation of plasmid DNA from Citrobacter freundii?
FAQ ID -885
表示
Do you have a protocol for the isolation of plasmid DNA from Corynebacterium glutamicum?
FAQ ID -886
表示
Do you have a protocol for the isolation of plasmid DNA from Borrelia spp.?
FAQ ID -884
表示
Do you have a protocol for the isolation of plasmid DNA from Lactobacillus spp.?
FAQ ID -887
表示
Do you have a protocol for the isolation of plasmid DNA from yeast?
FAQ ID -853
表示
Do you have a protocol for the isolation of single-stranded DNA from M13 phage using QIAGEN Plasmid Kits?
FAQ ID -894
表示
Do you have a protocol for the isolation of plasmid DNA from Staphylococcus spp.?
FAQ ID -890
表示
Do you have a protocol for the isolation of plasmid DNA from Oligotropha carboxidovorans?
FAQ ID -888
表示
Do you have a protocol for the isolation of plasmid DNA from Proteus spp.?
FAQ ID -889
表示
What are your recommendations for cotransfecting several plasmids?
FAQ ID -124
表示
What are the recommended culture and buffer volumes for a very low-copy plasmid?
FAQ ID -168
表示
Is mRNA isolation necessary for sensitive RT-PCR?
FAQ ID -111
表示
When should carrier be used with the QIAamp DNA Mini or the DNeasy Blood & Tissue Kit?
FAQ ID -100
表示
Which Anti-His Antibody is the most sensitive for my protein of interest?
FAQ ID -172
表示
Why do I have to add beta-mercaptoethanol (beta-ME) to lysis Buffer RLT of the RNeasy Kits?
FAQ ID -101
表示
What is the recommended culture medium for the QIAprep System?
FAQ ID -154
表示
How can I eliminate contaminating protein in my Ni-NTA 6xHis-tag protein purification?
FAQ ID -102
表示
How can I purify very small amounts of 6xHis-tagged protein using Ni-NTA technology?
FAQ ID -134
表示
How can I improve ligation efficiency of DNA from a QIAEX II Gel Extraction Kit?
FAQ ID -141
表示
How can I isolate RNA from 1 gram of plant tissue?
FAQ ID -128
表示
How can I improve the performance of the HiSpeed QIAprecipitator module?
FAQ ID -144
表示
What can I use to isolate RNA smaller than 200 nucleotides?
FAQ ID -115
表示
What epitopes do the Anti-His Conjugates and Anti-His Antibodies recognize?
FAQ ID -170
表示
What are the maximum culture volumes to use with the QIAGEN Plasmid Midi or Maxi Kit?
FAQ ID -167
表示
How should RNeasy Kits be stored and how long are they stable?
FAQ ID -103
表示
Is it possible to cleave the 6xHis-tag from an expressed protein?
FAQ ID -140
表示
How should QIAGEN Plasmid Purification Kits be stored and for how long?
FAQ ID -192
表示
What are the features and benefits of the QIAexpress 6xHis Tag System?
FAQ ID -193
表示
Do you have transfection data for QIAGEN Transfection Reagents?
FAQ ID -158
表示
Do you have data showing effects of sample size on DNA yield and purity using the DNeasy 96 Blood & Tissue kit?
FAQ ID -129
表示
Does QIAGEN offer vectors for direct cloning of PCR products?
FAQ ID -146
表示
How can I avoid variable transfection efficiencies with SuperFect Reagent?
FAQ ID -179
表示
Can DyeEx be used to clean up labeled DNA other than sequencing templates?
FAQ ID -137
表示
Are QIAamp DNA isolation kits suitable for apoptosis studies?
FAQ ID -149
表示
Can I use a QIAfilter Cartridge for purifying large plasmids?
FAQ ID -121
表示
Can I use Omniscript or Sensiscript RT's at a higher temperature?
FAQ ID -116
表示
How do you ensure that RNeasy buffers are RNase-free?
FAQ ID -113
表示
How can I purify DNA from soil, food and sewage samples for PCR?
FAQ ID -118
表示
How should I store Anti·His and Tag·100 Antibodies?
FAQ ID -194
表示
How do I prepare an insert for pQE vectors?
FAQ ID -185
表示
How can I obtain DNA-free RNA using an RNeasy Midi or Maxi Kit?
FAQ ID -143
表示
What are the compatibilities of different reagents with Ni-NTA matrices?
FAQ ID -49
表示
How can I prevent running out of M48 Kit reagents before the full number of samples are processed?
FAQ ID -1042
表示
Do you have a protocol for the isolation of genomic DNA from paraffin-embedded samples on the BioRobot M48?
FAQ ID -1019
表示
Is the TurboCapture Microplate Holder Type B compatible with the Biomek FX robotic workstation?
FAQ ID -1040
表示
Is there a limit to the size of proteins that can be purified using the Qproteome Glycoprotein Kits?
FAQ ID -1071
表示
Is it possible to scale up QuantiTect Reverse Transcription reactions to allow use of larger amounts of RNA?
FAQ ID -1063
表示
Is it possible to use the PhosphoProtein Purification Kit in batch format?
FAQ ID -1069
表示
What are the recommended storage conditions for the QuantiTect Reverse Transcription Kit and its components?
FAQ ID -1077
表示
What is the difference between TurboCapture Microplate Holders Type A and Type B?
FAQ ID -1038
表示
What blocking reagents do you recommend for chemiluminescent detection using Penta-, Tetra-, and RGS-His antibodies?
FAQ ID -1093
表示
Is Factor SB of the HotStar HiFidelity Polymerase Kit the same as Factor MP of the QIAGEN Multiplex PCR Kit?
FAQ ID -1049
表示
How can I transfect siRNA into insect cells such as Drosophila melanogaster S2?
FAQ ID -1046
表示
How can I tell TurboCapture Microplate Holder Type A from Type B?
FAQ ID -1039
表示
How much template can I use in the reaction and what is the maximum volume of template that can be used in the QuantiTect Kits?
FAQ ID -1086
表示
How much dye-labeled siRNA should I use to monitor transfection efficiency when using HiPerfect Transfection Reagent?
FAQ ID -1058
表示
What is the error rate of HotStar HiFidelity DNA Polymerase?
FAQ ID -1048
表示
Which QIAGEN kit do you recommend for purifying plasmid DNA suitable for transfection of sensitive cells?
FAQ ID -1092
表示
Which kit should I use for RNA isolation from Cartilage?
FAQ ID -1026
表示
Where can I find the serial number on QIAGEN's BioRobots?
FAQ ID -1064
表示
Which kit can be used for simultaneous purification of DNA and RNA from biopsies?
FAQ ID -1089
表示
Why is there RNA in the DNA eluate when using the AllPrep DNA Mini Spin Column?
FAQ ID -1044
表示
Why does my PCR product show up later when comparing the QuantiTect SYBR Green PCR Kits with Roche kits using the same annealing temperature?
FAQ ID -1083
表示
Will the "classic" RNeasy Mini Kit be discontinued after the launch of the Allprep DNA/RNA Mini Kit?
FAQ ID -1054
表示
Why does TA/UA cloning work with your proofreading HotStar HiFidelity DNA Polymerase?
FAQ ID -1053
表示
Why do melting temperatures differ between PCR fragments amplified with QIAGEN's QuantiTect SYBR Green PCR Kits and Roche Kits?
FAQ ID -1084
表示
What is the range of melting temperatures for the QuantiTect Primer Assay amplicons in the dissociation curve?
FAQ ID -1079
表示
What is the protein loading capacity per column of the Qproteome Albumin/IgG Depletion Kit?
FAQ ID -1090
表示
What is your recommendation for cleaning the TissueLyser Bead Dispenser (96-well format)?
FAQ ID -1055
表示
What vacuum pressure should be applied using the QIAvac 24 Plus for the QIAamp DSP Virus Kit and Blood Mini Kit Protocols?
FAQ ID -1033
表示
What is the resin in the Qproteome Murine Albumin and Qproteome Albumin/IgG Depletion Kits?
FAQ ID -1034
表示
How can I prevent clogging of QIAfilter cartridges?
FAQ ID -1060
表示
What is the volume of the eluate when using either spin or vacuum procedures with the QIAprep 96 Turbo Miniprep Kit?
FAQ ID -1067
表示
Do I have to use a ramp time of 2°C/sec on the LightCycler when using Quantitect Primer Assays?
FAQ ID -1065
表示
Does an activation time of 15 minutes influence the performance of the HotStarTaq Plus DNA Polymerase?
FAQ ID -1050
表示
Do you have a protocol for the isolation of RNA from bacterial cultures using RNAprotect Bacteria Reagent and QIAzol Lysis Reagent?
FAQ ID -1020
表示
Do you have a protocol for the isolation of DNA from mouse tails using MagAttract technology on BioRobot M96?
FAQ ID -1007
表示
Do you have a protocol for the isolation of DNA from forensic samples using the BioRobot M48?
FAQ ID -1017
表示
Can the USB Port of the BioSprint 96 instrument be used to transfer programs from a PC to the instrument?
FAQ ID -1032
表示
Are your FlexiTube siRNAs preferentially designed to any particular region of the target gene?
FAQ ID -1091
表示
Can PCR fragments generated with the EasyXpress Linear Template Kit be cloned into the pIX4.0 vector of the EasyXpress Protein Synthesis Insect Kit?
FAQ ID -1078
表示
Can the QProteome O-Glycan Glycoprotein Kits be used for blood cells?
FAQ ID -1036
表示
Can the Reverse Transcriptases of the QuantiTect Reverse Transcription Kit and the QuantiTect Probe RT-PCR Kit be used interchangeably?
FAQ ID -1066
表示
Can the AllPrep RNA/Protein Kit be used with tissue?
FAQ ID -1095
表示
Can the Blocking Reagent supplied with the Penta-His HRP Conjugate be used with other antibodies?
FAQ ID -1073
表示
How can air bubbles in PhosphoProtein Purification Columns be avoided?
FAQ ID -1070
表示
How can I increase low-copy plasmid DNA yields using QIAfilter Plasmid Kits?
FAQ ID -1062
表示
How can I ensure complete genomic DNA removal when using the RNase-Free DNase Set?
FAQ ID -1087
表示
Do you have information on the reproducibility of DNA yields from blood using the M48 BioRobot?
FAQ ID - 1004
表示
Do you have a protocol for transient transfection of HEK 293 cells in 75 cm3 flasks?
FAQ ID -1014
表示
Do you have a protocol for transient transfection of cells in 96-well plates using PolyFect Transfection Reagent?
FAQ ID -1013
表示
Do you have a protocol for transient transfection of HeLa-S3 cells in 60 mm dishes using PolyFect?
FAQ ID -1012
表示
Do you have a protocol for the isolation of total nucleic acids from cells on the M48 BioRobot?
FAQ ID -1009
表示
Do you have a protocol for vacuum processing of blood samples with the QIAamp DNA Blood Midi or Maxi Kits?
FAQ ID -1011
表示
Do you have a protocol for the isolation of total nucleic acids from tissue on the M48 BioRobot?
FAQ ID -1008
表示
Do you have information on realtime RT-PCR performance of RNA isolated from monocytes on the M48 BioRobot?
FAQ ID -1010
表示
Do you have information on DNA yields from blood with variable numbers of white blood cells using the M48 BioRobot?
FAQ ID -1006
表示
Do you have information on PCR template preparation from preserved blood samples on the M48 BioRobot?
FAQ ID - 1003
表示
Can the PAXgene Blood RNA Tubes undergo freeze/thaw cycles?
FAQ ID -2471
表示
If I want to use BioMag particles, do I have to buy a QIAGEN magnet too or can I use one that I already have?
FAQ ID -266
表示
Should I use Omniscript or Sensiscript for reverse transcription of low-copy mRNA?
FAQ ID -297
表示
What are the main differences between other magnetic beads and the BioMag particles?
FAQ ID -272
表示
My BioMag is about to expire, is it still any good?
FAQ ID -268
表示
How magnetically responsive is BioMag?
FAQ ID -265
表示
If I am using BioMag Streptavidin to capture biotinylated oligos, how can I then remove the oligos?
FAQ ID -279
表示
Why is an ice-incubation step included during reaction set-up when following the QuantiTect RT-PCR but not the QuantiTect PCR protocol.
FAQ ID -283
表示
What sequencing primers can I use with the pDrive cloning vector of the QIAGEN PCR Cloning Kit?
FAQ ID -292
表示
What is the difference between the QIAamp MinElute Virus Spin and the MinElute Virus Vacuum Kit?
FAQ ID -295
表示
What is the difference between the Fc specific versions of your secondary antibody BioMag particles and the non-specific?
FAQ ID -275
表示
Can I use my own cycling conditions with the QIAGEN Multiplex PCR Kit?
FAQ ID -287
表示
Can I select FITC labeled cells with BioMag?
FAQ ID -278
表示
Can I use BioMag particles with any specific primary antibody?
FAQ ID -273
表示
Are BioMag particles stable in other solvents?
FAQ ID -267
表示
Can BioMag be used for positive and negative selection?
FAQ ID -269
表示
How can I avoid poor immunolocalization morphology with Anti-His Antibodies?
FAQ ID -200
表示
How can I prevent non-specific binding when using BioMag?
FAQ ID -277
表示
How do I prevent bubbles from forming in my Ni-NTA agarose column?
FAQ ID -285
表示
How can I purify mRNA from total RNA using an Oligotex Direct mRNA Kit?
FAQ ID -201
表示
Is your Nuclease-Free Water fluorescence-free?
FAQ ID -1291
表示
What quality level does your Nuclease-Free Water have?
FAQ ID -1292
表示
How should the GelPilot DNA Loading Dye be handled?
FAQ ID -1287
表示
Does GelPilot DNA Loading Dye contain ethidium bromide?
FAQ ID -1286
表示
Can phenol/chloroform be placed in the MaXtract tube for extraction at a later time?
FAQ ID -1299
表示
Are MaXtract tubes siliconized?
FAQ ID -1298
表示
Should I input the dilution factor of my samples into the LiquiChip Analyser Software dilution factors of samples?
FAQ ID -1211
表示
What cell lines have been tested with the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1205
表示
Is a saliva collection device provided in the RNeasy Protect Saliva Mini Kit?
FAQ ID -1213
表示
Is it possible to increase nucleic acid concentrations when following protocols on the BioRobot EZ1?
FAQ ID -1232
表示
Is RNAprotect Cell Reagent provided in the RNeasy Protect Cell Kit available separately?
FAQ ID -1217
表示
Is it possible to use QIAGEN's pQE-Trisystem Vector with the EasyXpress Insect Kit II?
FAQ ID -1225
表示
What vector do you recommend as template for in-vitro protein expression with the EasyXpress Insect Kit II?
FAQ ID -1224
表示
What type of promoter should my template have for in-vitro protein expression with the EasyXpress Insect Kit II?
FAQ ID -1223
表示
What is the maximum number of cells that can be used with the AllPrep RNA/Protein Kit ?
FAQ ID -1208
表示
Will the Qproteome Plasma Membrane Protein Kit work with starting materials other than adherent mammalian cells?
FAQ ID -1202
表示
What is the difference between various FlexiTube siRNAs listed for the same target gene, and which one should I choose?
FAQ ID -1206
表示
What is the protein yield when using the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1201
表示
What is the size of the BioRobot EZ1?
FAQ ID -1245
表示
Does anything have to be added to express post-translational modifications (PTMs) with the EasyXpress Insect Kit II?
FAQ ID -1226
表示
Do you have a protocol for isolating cytoplasmic RNA from animal cells using the RNeasy Mini Kit?
FAQ ID -1207
表示
Do you have a protocol for purification of miRNA from animal cells using the RNeasy Plus Mini Kit and RNeasy MinElute Cleanup Kit?
FAQ ID -1258
表示
Can cells stabilized with RNAprotect Cell Reagent be used for cell sorting by flow cytometry (FACS)?
FAQ ID -1216
表示
Can glycosylated proteins be expressed using the EasyXpress Insect Kit II?
FAQ ID -1227
表示
Can RNAprotect Saliva Reagent be purchased separately?
FAQ ID -1214
表示
Can you recommend a Reagent or Kit for stabilizing RNA in cultured cells?
FAQ ID -1215
表示
Can the Strep-Tactin Magnetic Beads of the Qproteome Plasma Membrane Protein Kit be reused?
FAQ ID -1204
表示
Can the Qproteome Plasma Membrane Protein Kit be used with tissue samples?
FAQ ID -1200
表示
Can the RLT lysate of the BioSprint DNA Plant protocol be stored frozen?
FAQ ID -1248
表示
How can I decontaminate the BioRobot EZ1?
FAQ ID -1231
表示
How do you ensure that concentrated RNA is purified from saliva using the RNeasy Protect Saliva Mini Kit?
FAQ ID -1212
表示
How much active protein can be expressed in-vitro using the EasyXpress Insect Kit II, and how much time does it take?
FAQ ID -1222
表示
How many freeze-thaw cycles can the various reaction mixes in the EasyXpress Insect Kit II tolerate?
FAQ ID -1219
表示
Do you have a protocol for the isolation of DNA from buccal cells using the BioRobot EZ1?
FAQ ID -1260
表示
Do you have a protocol for transfection of differentiated macrophage cell lines (THP) with siRNA?
-1
表示
How are plasma membrane containing vesicles eluted off the ligand in the Qproteome Plasma Membrane Protein procedure?
FAQ ID -1203
表示
Which fixation method is used in the PAXgene Tissue System?
FAQ ID - 3600
表示
What is the fixation reagent of PAXgene Tissue FIX?
FAQ ID - 3601
表示
What is the stabilization reagent of PAXgene Tissue STABILIZER?
FAQ ID - 3602
表示
What is the maximum tissue size that can be fixed in a PAXgene Tissue FIX Container (50 ml)?
FAQ ID - 3604
表示
Why are two reagents used in the PAXgene Tissue System?
FAQ ID - 3603
表示
Which conditions are recommended for the storage of tissues in PAXgene Tissue STABILIZER?
FAQ ID - 3605
表示
Is it possible to process formalin-fixed and PAXgene Tissue fixed samples together in one run?
FAQ ID - 3606
表示
Is it necessary to clean a processor normally used for formalin-fixed tissue before using it with PAXgene Tissue fixed tissue?
FAQ ID - 3607
表示
Is it possible to integrate the PAXgene Tissue STABILIZER into tissue processing?
FAQ ID - 3608
表示
Are immunohistochemistry (IHC) assays developed for formalin-fixed, paraffin-embedded (FFPE) tissues compatible with PAXgene Tissue fixed, paraffin-embedded (PFPE) tissues?
FAQ ID - 3609
表示
How well is RNA integrity preserved in PAXgene Tissue fixed, paraffin-embedded (PFPE) tissue?
FAQ ID - 3611
表示
Is it possible to use formalin-fixed, paraffin-embedded (FFPE) kits and protocols to isolate biomolecules from PAXgene Tissue fixed, paraffin-embedded (PFPE) tissue?
FAQ ID - 3610
表示
How well is DNA integrity preserved in PAXgene Tissue fixed, paraffin-embedded (PFPE) tissue?
FAQ ID - 3612
表示
Are special kits and protocols required to isolate biomolecules from PAXgene Tissue fixed, cryo-embedded (PFCE) tissue?
FAQ ID - 3614
表示
What are the yield and integrity of nucleic acids isolated from blocks of PAXgene Tissue fixed, cryo-embedded (PFCE) tissue?
FAQ ID - 3613
表示
Can proteins be extracted from PAXgene Tissue fixed specimens?
FAQ ID - 3616
表示
Does the PAXgene Tissue RNA Kit co-purify small RNAs?
FAQ ID - 3615
表示
Which kits and protocols can be used to isolate nucleic acids from microdissected PAXgene Tissue fixed, paraffin-embedded (PFPE) and PAXgene Tissue fixed, cryo-embedded (PFCE) specimens?
FAQ ID - 3617
表示
What is the PCR performance of DNA purified from PAXgene Tissue fixed, paraffin-embedded (PFPE) and PAXgene Tissue fixed, cryo-embedded (PFCE) tissue compared to DNA from snap frozen or formalin-fixed, paraffin-embedded (FFPE) tissue?
FAQ ID - 3618
表示
How is the quality of proteins purified from PAXgene Tissue fixed and stabilized tissue?
FAQ ID - 3619
表示
Can the RNeasy kits be used to extract RNA from saliva collected using the Oragene collection kit?
FAQ ID - 3623
表示
How do I analyze codon 61 mutations with the RAS extension kit (cat. no. 971590)?
FAQ ID - 3622
表示
Are QR codes recognized by QIAsymphony?
FAQ ID - 3625
表示
Do I need to use a blood collection set with the PAXgene Blood ccfDNA Tube?
FAQ ID - 3626
表示
What is the reagent in the PAXgene Blood ccfDNA Tube?
FAQ ID - 3632
表示
Does the insert sequence provided in the specification sheet correspond to the target sequence or to anti-sense sequence?
FAQ ID - 3627
表示
What is the shelf life of unused PAXgene Blood ccfDNA Tubes?
FAQ ID - 3633
表示
How should unused PAXgene Blood ccfDNA Tubes be stored?
FAQ ID - 3634
表示
Are there special considerations for phlebotomy when using the PAXgene Blood ccfDNA Tube (blood collection set, discard tube, positioning of the tube, issues with short draws, etc.)?
FAQ ID - 3635
表示
Are PAXgene Blood ccfDNA Tubes sterile?
FAQ ID - 3636
表示
What is the expected ccfDNA yield from plasma generated from 10 ml of blood?
FAQ ID - 3637
表示
Can I use plasma from underfilled PAXgene Blood ccfDNA Tubes?
FAQ ID - 3638
表示
How long can whole blood stabilized in PAXgene Blood ccfDNA Tubes be stored at room temperature?
FAQ ID - 3639
表示
Can whole blood in PAXgene Blood ccfDNA Tubes be stored at temperatures above 25°C?
FAQ ID - 3640
表示
Can whole blood in PAXgene Blood ccfDNA Tubes be stored at temperatures below 15°C?
FAQ ID - 3641
表示
Can whole blood be frozen in PAXgene Blood ccfDNA Tubes?
FAQ ID - 3642
表示
Is double centrifugation required for plasma processing?
FAQ ID - 3643
表示
How long and at which temperature can plasma generated from whole blood in PAXgene Blood ccfDNA Tubes be stored?
FAQ ID - 3644
表示
What should I do if cryoprecipitates form while thawing a frozen plasma sample?
FAQ ID - 3646
表示
Which plasma volumes can I process with the QIAsymphony PAXgene Blood ccfDNA protocols?
FAQ ID - 3648
表示
How many extractions can I perform with a QIAsymphony PAXgene Blood ccfDNA Kit, using the 2.4 ml or the 4.8 ml protocols?
FAQ ID - 3649
表示
How long after first use can a reagent cartridge be stored for further use?
FAQ ID - 3650
表示
For what type of sample material is the QIAsymphony PAXgene Blood ccfDNA Kit intended?
FAQ ID - 3652
表示
Which tubes are recommended for the QIAsymphony sample rack
FAQ ID - 3653
表示
Which protocol line should I use to process plasma samples?
FAQ ID - 3654
表示
Does the QIAsymphony PAXgene Blood ccfDNA Kit also allow eluting ccfDNA in less than 60 µl?
FAQ ID - 3656
表示
How should eluates produced with the PAXgene Blood ccfDNA System be stored?
FAQ ID - 3657
表示
Which downstream applications have been tested with ccfDNA purified from whole blood collected and processed with the PAXgene Blood ccfDNA System?
FAQ ID - 3658
表示
What is the shelf life of the QIAsymphony PAXgene Blood ccfDNA Kit?
FAQ ID - 3651
表示
Which elution volumes are available with the QIAsymphony PAXgene Blood ccfDNA Kit?
FAQ ID - 3655
表示
Why is a blood collection set required to collect blood into the PAXgene Blood ccfDNA Tube?
FAQ ID - 3628
表示
Can reagent from the PAXgene Blood ccfDNA Tube flow back into the patient’s arm?
FAQ ID - 3629
表示
Can I use a different brand blood collection set with the PAXgene Blood ccfDNA Tube?
FAQ ID - 3630
表示
What is the blood draw volume of the PAXgene Blood ccfDNA Tube
FAQ ID - 3631
表示
What is the difference between RT² Profiler PCR Array and RT² Profiler PCR Array PLUS version?
FAQ ID - 3685
表示
Where can I find the gene list for a specific RT² Profiler PCR Array?
FAQ ID - 3684
表示
Is it possible to store nucleic acids extracted using the SpeedXtract Virus Kit?
FAQ ID - 3680
表示
Total RNA from what sample types are compatible with the QIAseq miRNA Library Kit?
FAQ ID - 3660
表示
Can miRNA sequencing libraries be prepared from total RNA isolated from heparinized plasma samples?
FAQ ID - 3661
表示
Are any components of the QIAseq miRNA Library Kit interchangeable with components from other QIAGEN kits?
FAQ ID - 3662
表示
Can I still perform sequencing if my miRNA sequencing library concentrations are too low to obtain a 4 nM library?
FAQ ID - 3666
表示
What method is used to eliminate adapter dimers from the QIAseq miRNA library?
FAQ ID - 3667
表示
Does a QIAseq miRNA library include hY4 Y RNA?
FAQ ID - 3670
表示
What is the sequence of the QIAseq miRNA NGS 3’ Adapter?
FAQ ID - 3671
表示
Do the covered regions in the BED file include the primers?
FAQ ID - 3689
表示
What do the GTIN, UDI and REF abbreviations mean on the label of any QIAGEN box?
FAQ ID - 3697
表示
Do eluates generated with the PAXgene Blood miRNA Kit contain residual genomic DNA?
FAQ ID - 3637
表示
Do you have a protocol for high-throughput purification of plasmid DNA using the BioRobot Universal System?
FAQ ID -1191
表示
Is the surface tension of the crystallization supports of the EasyXtal 15-Well Tools similar to that of a siliconized cover slide?
FAQ ID -1107
表示
Is the pH indicated in the formulation sheet for Screening Suite buffers the final pH?
FAQ ID -1123
表示
What are the applications the EasyXtal 15-Well Tool can be used for?
FAQ ID -1111
表示
Is the EasyXtal Tool compatible with liquid-handling systems and visualization robots?
FAQ ID -1118
表示
Is it possible to collect intact mitochondria before or after the density gradient centrifugation step of the Qproteome Mitochondria Isolation protocol?
FAQ ID -1187
表示
What cell lines have been tested with the Fastlane Cell cDNA Kit?
FAQ ID -1175
表示
What does 'QIAGEN Certified Solution' for Protein Crystallization mean?
FAQ ID -1121
表示
How many protein crystallization conditions are available at QIAGEN?
FAQ ID -1119
表示
How much detection reagent do you generally recommend for LiquiChip Assays?
FAQ ID -1159
表示
How many cells can be used with the Qproteome Mitochondria Isolation Kit, and how much mitochondrial protein can be expected?
FAQ ID -1189
表示
How many drops can be set up on a protein crystallization support?
FAQ ID -1110
表示
How many LiquiChip beads are recommended for an xMAP experiment?
FAQ ID -1161
表示
How much solution can I add to an EasyXtal 15-Well Tool reservoir well?
FAQ ID -1114
表示
In which formats are crystallization condition Screening Suites available?
FAQ ID -1127
表示
If I cannot find a QuantiTect Primer Assay for my target gene in rat, can I use the assays for the orthologous genes in mouse and human?
FAQ ID -1145
表示
If a QuantiTect Primer Assay has more than one version number, does this mean that earlier assay versions may not work?
FAQ ID -1136
表示
How sensitive is the LiquiChip Reader?
FAQ ID -1157
表示
How much time is needed for a LiquiChip assay point measurement?
FAQ ID -1162
表示
Why are there various different QuantiTect Primer Assays for my gene (previous versions, transcript variants)?
FAQ ID -1133
表示
What is the delivery time for QuantiTect Primer Assays?
FAQ ID -1142
表示
Where can I find the composition tables for solutions used in individual Crystallization Screening Suites?
FAQ ID -1124
表示
What kind of strategy for initial screening of protein crystallization conditions do you recommend?
FAQ ID -1120
表示
When searching for a QuantiTect Primer Assay for my gene of interest, why do I only find the assay for human but not for rat?
FAQ ID -1139
表示
What type of magnet do you recommend for handling the magnetic beads in the Qproteome Plasma Membrane Protein protocol?
FAQ ID -1193
表示
What starting material can be used with the Qproteome Mitochondria Isolation Kit?
FAQ ID -1184
表示
Can the EZ1 DNA Investigator Tip Dance protocol cope with any solid matrix remaining in the sample tube?
FAQ ID -1153
表示
Are EasyXtal 15-Well Tools stackable?
FAQ ID -1116
表示
Why can I not find the QuantiTect Primer Assay in GeneGlobe that I had previously ordered from QIAGEN?
FAQ ID -1138
表示
Which QuantiTect Primer Assay should I choose for my gene of interest?
FAQ ID -1135
表示
Why does the QuantiTect Primer Assay for my gene of interest have only one version number?
FAQ ID -1134
表示
Which chemical products do you use to prepare screening solutions for protein crystallization?
FAQ ID -1122
表示
Will proteins eluted in the Qproteome Plasma Membrane Protein protocol be modified, e.g. with the ligand?
FAQ ID -1195
表示
Will the ligand in the Qproteome Plasma Membrane Protein protocol be specific for plasma membrane exclusively?
FAQ ID -1198
表示
Will integral, peripheral as well as lipid-anchored plasma membrane proteins be isolated with the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1199
表示
Why is there no QuantiTect Primer Assay for my gene of interest?
FAQ ID -1140
表示
What is the EasyXtal 15-Well Tool made of?
FAQ ID -1106
表示
What is the dynamic range of detection of the LiquiChip Reader?
FAQ ID -1158
表示
Can the nuclei and cell debris fraction generated in the QProteome Mitochondria isolation procedure be used for further fractionation?
FAQ ID -1185
表示
Can the EZ1 DNA Forensic Card be used with the EZ1 DNA Investigator Kit?
FAQ ID -1151
表示
Can the EasyXtal 15-Well Tools be reused?
FAQ ID -1117
表示
Can the Qproteome Plasma Membrane Protein Kit be used with suspension cells?
FAQ ID -1194
表示
Can your Tag antibody recognize rat MAPK1 also?
-100
表示
Can xMAP kits from other Luminex partners be used on the LiquiChip System purchased from QIAGEN?
FAQ ID -1156
表示
Can the remaining fractions obtained in the Qproteome Plasma Membrane Protein procedure be used in downstream assays?
FAQ ID -1197
表示
Can the Spin Columns of the Qproteome Albumin/IgG Depletion Kit be reused?
FAQ ID -1173
表示
Are scoring sheets available for each crystallization condition Screening Suite?
FAQ ID -1125
表示
Can mitochondria separated with the Qproteome Mitochondria Isolation Kit be used for downstream DNA isolation?
FAQ ID -1188
表示
Are protein modifications such as glycosylation problematic when using the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1196
表示
Can acetone be used for precipitation of protein from Buffer RLT lysates generated with RNeasy Kits?
FAQ ID -1164
表示
Can I increase the annealing temperature recommended for QuantiTect Primer Assays used with the QuantiTect SYBR Green PCR Kits?
FAQ ID -1146
表示
How are NeXtal deep-well blocks sealed? Can they be resealed?
FAQ ID -1128
表示
Does the EasyXtal Tool conform to an SBS format?
FAQ ID -1115
表示
Do you have WGA protocols for starting materials not mentioned in the REPLI-g Handbooks?
FAQ ID -1160
表示
How easy is it to scoop up a protein crystal with the lip around the crystallization supports of the EasyXtal 15-Well Tools?
FAQ ID -1113
表示
Do you have a protocol for the purification of 6xHis-tagged proteins using BioSprint?
FAQ ID -1167
表示
How did you determine that your AllStar Negative Control siRNA binds to RISC?
FAQ ID -1180
表示
How is the quality of the crystallization condition Screening Suites guaranteed?
FAQ ID -1126
表示
How do I use EasyXtal Crystallization Tools?
FAQ ID -1105
表示
How does the sealing efficiency of the crystallization supports of the EasyXtal 15-Well Tool compare to grease?
FAQ ID -1109
表示
Do you have a kit for protein isolation from mitochondria prepared with your Qproteome Mitochondria Isolation Kit?
FAQ ID -1190
表示
Do you have a kit for the isolation of RNA from formalin-fixed, paraffin-embedded samples?
FAQ ID -1174
表示
Do I need an ultracentrifuge for the density gradient centrifugation step in the Qproteome Mitochondria Isolation protocol?
FAQ ID -1186
表示
Do protein crystals stick to the walls of cavities when using the DropGuard crystallization supports?
FAQ ID -1108
表示
Do you have a protocol for evaluating pipetting accuracy of the BioRobot EZ1?
FAQ ID -1131
表示
Do you have a protocol for purification of DNA from stool samples for pathogen detection using BioSprint Instruments?
FAQ ID -1165
表示
Do you have a protocol for purification of DNA from stool samples using BioSprint Instruments?
FAQ ID -1166
表示
Do you have a protocol for evaluating temperature accuracy of the BioRobot EZ1?
FAQ ID -1168
表示
Which competent E. coli cells should I use to amplify the SureSilencing shRNA Plasmids?
FAQ ID -2890
表示
Which analyses can be performed with the PyroMark Q96 ID software version 1.0?
FAQ ID -2845
表示
Does the same U1 promoter in the SureSilencing shRNA Plasmids express shRNA in human, mouse, and rat cell lines?
FAQ ID -2887
表示
How can I use the SureSilencing shRNA Plasmids for stable transfection and knock down in a cell line that is already resistant to both neomycin and puromycin?
FAQ ID -2895
表示
Can I use my own siRNA design?
FAQ ID -2897
表示
Can I order the nucleotides from PyroMark Gold Reagents separately?
FAQ ID -2827
表示
Can I reclone the insert sequences from the SureSilencing shRNA Plasmids into a viral-based vector?
FAQ ID -2896
表示
Can I directly transfect SureSilencing shRNA Plasmids into my cells?
FAQ ID -2899
表示
Do any of the SureSilencing shRNA Plasmids contain inducible promoters?
FAQ ID -2888
表示
Can PyroMark Gold reagents be vortexed?
FAQ ID -2844
表示
What are the features of the new PyroMark Q96 ID software 2.5?
FAQ ID -2867
表示
What cell line does QIAGEN use for quality control testing of the SureSilencing shRNA Plasmids?
FAQ ID -2885
表示
Should I use the SureSilencing shRNA Plasmids with the neomycin-resistance marker, the puromycin-resistance marker, or the GFP reporter gene?
FAQ ID -2882
表示
What else do I need to complete an experiment using the SureSilencing shRNA Plasmids?
FAQ ID -2889
表示
What cell lines can I use with the SureSilencing shRNA Plasmids?
FAQ ID -2891
表示
How long should I wait after transfection before enriching my transfected cells, validating knock down, and looking for phenotypic changes?
FAQ ID -2893
表示
Is the expression level of miRNA precursors lower compared to that of mature miRNAs?
FAQ ID -2807
表示
How many times can the CDTs, NDTs, and RDTs be used?
FAQ ID -2865
表示
What is the PyroMark Q96 Data Converter?
FAQ ID -2868
表示
What is the pyrosequencing data exchange tool for?
FAQ ID -2864
表示
What is the composition of Buffer APP?
FAQ ID -2804
表示
What is the composition of Buffer FRN?
FAQ ID -2802
表示
What is the composition of Buffer APL?
FAQ ID -2803
表示
Which analyses can be performed with the PyroMark Q96 MD software?
FAQ ID -2866
表示
Which PyroMark Gold Q96 Reagent should be used for which instrument and application?
FAQ ID -2836
表示
What is the SureSilencing shRNA Plasmids guarantee?
FAQ ID -2898
表示
What primers may I use to sequence the shRNA cassette within the SureSilencing shRNA Plasmids?
FAQ ID -2886
表示
Does the PyroMark CpG LINE assay target mouse transposons as well?
-1
表示
How do I find the SureSilencing shRNA Plasmids for my gene of interest?
FAQ ID -2883
表示
How are the SureSilencing shRNA Plasmids shipped?
FAQ ID -2884
表示
What is the concentration of SureENTRY Transduction Reagent?
FAQ ID - 3708
表示
Is it possible to get a Custom RT2 Profiler PCR Array, cat. # 330131, with primer assays targeting transcripts of different species, e.g. assays targeting transcripts from mouse and assays targeting transcripts from human, on one plate?
FAQ ID - 3710
表示
Is it possible to purchase Buffer VXL which is part of the QIAamp cador Pathogen Mini Kit, (Cat No.: 54104, 54106) separately?
FAQ ID - 3712
表示
What sample tubes can I use on my QIAsymphony SP system?
FAQ ID - 3713
表示
How can I decontaminate my QIAsymphony SP / AS system?
FAQ ID - 3714
表示
Can other QIAGEN buffers from non-UCP kits (e.g. AW1 instead of AUW1) be used with the QIAamp UCP DNA Micro Kit (cat. no. 56204)?
FAQ ID - 3717
表示
How is the Pyromark Q48 cartridge to be cleaned?
FAQ ID - 3718
表示
Can the disc and absorber strips for the Pyromark Q48 be reused?
FAQ ID - 3720
表示
What is the dead volume of the cartridges in PyroMark Q48?
FAQ ID - 3719
表示
How much DNA is needed in the PyroMark Q48?
FAQ ID - 3721
表示
Can I use PyroMark Q48 for diagnostics?
FAQ ID - 3722
表示
Can I transfer my assays from PyroMark Q24/Q96 to PyroMark Q48 Autoprep?
FAQ ID - 3723
表示
Can I analyze my Next Generation Sequencing (NGS) samples on the QIAxcel for Quality control?
FAQ ID - 3724
表示
Is an additional proteinase K digest possible with DNeasy PowerSoil Kit and DNeasy PowerLyzer Kit?
FAQ ID - 3725
表示
Can I buy the 1 ml Bead Plates from the DNeasy UltraClean 96 Microbial Kit (384) separately?
FAQ ID - 3726
表示
Does QIAGEN offer an anti-GFP gapmer control?
FAQ ID - 3739
表示
Why do I observe a CT shift for the Internal Control in some samples in comparison to the CT value for the Internal Control of the dilution series of the Male Control DNA M1?
FAQ ID - 3745
表示
How long can I store the dilutions of the Male Control DNA M1 standards at 2–8°C?
FAQ ID - 3744
表示
Do I need to buy special kits for the QIAcube Connect?
FAQ ID - 141485
表示
Can I program my own protocols for the QIAcube Connect?
FAQ ID - 141486
表示
Can the QIAcube Connect rotor and/or buckets be removed for cleaning?
FAQ ID - 141491
表示
Can purification columns from other suppliers be processed on the QIAcube Connect?
FAQ ID - 141487
表示
How can I get software updates for the QIAcube Connect?
FAQ ID - 141494
表示
Is it necessary to place the lids of the elution tube and column into the slots of the rotor adapter during processing on the QIAcube Connect?
FAQ ID - 141496
表示
Do I need to discard partially used QIAcube Connect tip racks?
FAQ ID - 141499
表示
How can I decontaminate the QIAcube Connect system?
FAQ ID - 141500
表示
Can the QIAcube Connect heater/shaker be used independently from protocol runs?
FAQ ID - 141502
表示
How can I load new protocols onto the QIAcube Connect?
FAQ ID - 141501
表示
What dedicated QIAcube Connect kits are available?
FAQ ID - 141504
表示
Do you have a protocol for the QIAprep Spin M13 Kit on the QIAcube Connect?
FAQ ID - 1414507
表示
Where can I find the ordering information for QIAcube Connect accessories such as shaker rack plugs, rack labeling strips, reagent bottle racks, 30 ml reagent bottles, rotor-adapter holder, rotor adapters, sample tubes CB, sample tubes RB and spin-column adapter rings?
FAQ ID - 141505
表示
Do you have a protocol for the AllPrep DNA/RNA/Protein Mini Kit on the QIAcube Connect?
FAQ ID - 141506
表示
Which QIAcube Connect standard protocol might be suitable to extract RNA from saliva or from a buccal cell pellet?
FAQ ID - 141508
表示
How often should the o-ring for the pipettor tip adapter be changed on the QIAcube Connect?
FAQ ID - 141509
表示
Can the CB and RB sample tubes be used interchangeably?
FAQ ID - 141510
表示
Which network settings are supported by the QIAcube Connect and Q-Base?
FAQ ID - 141517
表示
Why can I not find the Q-Base device in the device list during the first installation?
FAQ ID - 141516
表示
Why can’t I see my QIAcube Connect instrument in the QIAcube Connect App?
FAQ ID - 1414518
表示
Why is the QIAcube Connect App reacting so slowly?
FAQ ID - 141519
表示
Why are not all applications/kits/protocol files visible in the run setup (QIAcube Connect App)?
FAQ ID - 1414520
表示
Why does the connection test fail?
FAQ ID - 141522
表示
How can I accurately determine the amount of input material for the EpiTect Hi-C Kit?
FAQ ID -
143065
表示
What sample source do you support?
FAQ ID -
143066
表示
How long does it take to complete the EpiTect Hi-C protocol?
FAQ ID -
143068
表示
How many reactions are in a kit?
FAQ ID -
143067
表示
Can I use cells that have been previously crosslinked and frozen (e.g., for a ChIP or ChIP-seq experiment) as input material for the EpiTect Hi-C protocol?
FAQ ID -
143069
表示
Can I substitute the endonuclease used in the Hi-C Digestion step with another endonuclease?
FAQ ID -
143070
表示
Are there stopping points in the Hi-C workflow?
FAQ ID -
143071
表示
With which platform can I perform my sequencing?
FAQ ID -
143072
表示
With which read length should the EpiTect Hi-C NGS libraries be sequenced
FAQ ID -
143073
表示
How do I know if my Hi-C sample is a good candidate for deep sequencing?
FAQ ID -
143074
表示
What kind of analysis does the EpiTect Hi-C Data Analysis Portal perform?
FAQ ID -
143076
表示
Can I use my own pipeline to analyze results from my EpiTect Hi-C experiments?
FAQ ID -
143078
表示
How critical is the time of the temperature change from 60°C to 80°C?
FAQ ID -
143768
表示
Is it possible to use Lyse&Spin baskets?
FAQ ID -
143762
表示
Why is DTT used only for semen samples?
FAQ ID -
143761
表示
Can the Repli-g Advanced DNA Single Cell Kit also be used for bacterial cells?
FAQ ID -
143079
表示
Can the lysis volume be reduced for higher sensitivity?
FAQ ID -
143763
表示
What if only one heater shaker is available?
FAQ ID -
143764
表示
Why is there no male DNA obtained from sexual assault samples?
FAQ ID -
143767
表示
If 400 µl are used as lysis volume, how do I concentrate the lysate? (Otherwise the DNA would be too diluted.)
FAQ ID -
143766
表示
Why is the QIAamp Viral RNA Mini Kit (50) currently unavailable?
FAQ ID -147395
表示
What RNAs has QIAseq FastSelect been designed to remove?
FAQ ID -147910
表示
How does QIAseq FastSelect work?
FAQ ID -147907
表示
Is QIAseq FastSelect truly as easy as combining a reagent with RNA and ramping down the temperature?
FAQ ID -147909
表示
Will QIAseq FastSelect work in other species?
FAQ ID -147911
表示
What library prep kits has QIAseq FastSelect been tested with?
FAQ ID -147912
表示
I am using an RNA library prep kit that is not listed in the QIAseq FastSelect handbook. Will QIAseq FastSelect work with my kit?
FAQ ID -147913
表示
What RNA range has the QIAseq FastSelect been tested with?
FAQ ID -147914
表示
Can QIAseq FastSelect Plant or QIAseq FastSelect Yeast be combined with FastSelect 5S/16S/23S?
FAQ ID -147915
表示
Is it possible to test the efficiency of FastSelect rRNA removal by using a Bioanalyzer, etc.?
FAQ ID -147916
表示
Is plasmid DNA purified with QIAGEN Plasmid Purification Kits suitable for in vitro transcription?
FAQ ID -1
表示
How should I quantify RNA isolated with RNeasy Kits?
FAQ ID -32
表示
When is chloramphenicol amplification of plasmids performed?
FAQ ID -3
表示
What are the expected DNA yields from different tissues using the QIAamp DNA Mini Kit?
FAQ ID -45
表示
What are the most commonly used protease inhibitors?
FAQ ID -53
表示
How should I propagate pQE expression plasmids?
FAQ ID -58
表示
How can I increase the amount of soluble recombinant protein in E. coli expression?
FAQ ID -64
表示
How can I remove imidazole from a protein sample?
FAQ ID -91
表示
Why does my isolated RNA have a low OD 260/280 ratio?
FAQ ID -97
表示
How can I avoid little or no RNA yields when using an RNeasy Kit?
FAQ ID -28
表示
Do I need to use an RNase inhibitor in my RT reaction?
FAQ ID -119
表示
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