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How can I identify the binding sites of my transcription factor using ChIP?
FAQ ID -2753
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At what point can I stop and freeze my samples when using ChIP?
FAQ ID -2754
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What is RNA interference (RNAi)?
FAQ ID -2755
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What are the key factors for success in an RNAi experiment?
FAQ ID -2758
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What criteria should one use in choosing between siRNA versus shRNA for their studies?
FAQ ID -2771
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How does stable transfection of a shRNA-encoding plasmid work?
FAQ ID -2779
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What are the SureSilencing shRNA Plasmids?
FAQ ID -2784
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What is the composition of Buffer S3?
FAQ ID -2788
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What is the composition of Buffer ETR?
FAQ ID -2789
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What is the composition of Buffer BB?
FAQ ID -2790
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What is the composition of Buffer RLT plus?
FAQ ID -2794
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What is the composition of Buffer RLC?
FAQ ID -2795
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What is the composition of Buffer RPE?
FAQ ID -2797
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What is the composition of Buffer RWT?
FAQ ID -2798
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What is the composition of gDNA Eliminator Solution?
FAQ ID -2799
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What is the composition of Buffer RDD?
FAQ ID -2800
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What is the composition of Buffer PKD?
FAQ ID -2801
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What is the composition of Buffer ALO?
FAQ ID -2805
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What is the composition of RBC Lysis Solution?
FAQ ID -2808
表示
What is the composition of Cell Lysis Solution?
FAQ ID -2809
表示
What is the composition of Protein Precipitation Solution?
FAQ ID -2810
表示
What is the composition of Cell Suspension Solution?
FAQ ID -2811
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What is the composition and concentration of Glycogen Solution in Gentra Puregene Kits?
FAQ ID -2812
表示
What is the composition of DNA Hydration Solution in Gentra Puregene Kits?
FAQ ID -2813
表示
What is the meaning of the abbreviations NDT and CDT and what are the differences?
FAQ ID -2841
表示
What are the changes of PyroMark Assay Design Software Version 2.0 compared to 1.0?
FAQ ID -2849
表示
Can I use fluorescence microscopy to assess the transfection efficiency of the SureSilencing shRNA Plasmids with GFP in my model cell line of interest?
FAQ ID -2894
表示
Do tissue samples require pretreatment before loading onto the QIAsymphony SP for DNA extraction?
FAQ ID -2926
表示
What is the composition of Buffer G2?
FAQ ID -2943
表示
What is the composition of Buffer B1?
FAQ ID -2944
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What is the composition of Buffer B2?
FAQ ID -2945
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How much DNA does a human cell contain?
FAQ ID -2948
表示
How much RNA does a bacterial cell contain?
FAQ ID -2949
表示
How much DNA and RNA can be expected from human blood cells?
FAQ ID -2950
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What is the cellular composition of human blood?
FAQ ID -2951
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How can I desalt and concentrate a protein fraction by trichloroacetic acid (TCA) precipitation?
FAQ ID -2954
表示
Is there a risk of crosstalk from the FAM channel to the VIC channel if the residual DNA target is present in very high copy numbers?
FAQ ID -2980
表示
Why is the final heat denaturation step so important with the QIAsymphony PAXgene Blood RNA protocol?
FAQ ID -2987
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What is the sequence of the miScript Universal Primer?
FAQ ID -2994
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How can I keep my centrifuge tubes endotoxin-free?
FAQ ID -301
表示
Can Buffers N3 and P3 be used interchangeably?
FAQ ID -310
表示
Are QIAprep and QIAquick Spin columns interchangeable?
FAQ ID -311
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Can I store agarose gel slices containing DNA for gel extraction at a later point?
FAQ ID -313
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How can QIAGEN Protease and Proteinase K be inactivated?
FAQ ID -315
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Does the 5x OneStep RT-PCR Buffer contain BSA?
FAQ ID -326
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What is the origin of replication and the plasmid copy number of the pQE vectors?
FAQ ID -338
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Is QIAGEN carrier RNA sold separately?
FAQ ID -351
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What is the white insoluble precipitate in my resuspended plasmid DNA pellet?
FAQ ID -352
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What is the composition of PBS?
FAQ ID -361
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How can I express toxic protein in E. coli?
FAQ ID -373
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How can I improve DNA yields from very tough tissues using the DNeasy Blood & Tissue Kit or the QIAamp DNA Mini Kit?
FAQ ID -374
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What are the dissociation constants for the Anti-His Antibodies?
FAQ ID -385
表示
What is the average molecular weight of a siRNA, and how do I convert uM to ug values?
FAQ ID -388
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Can siRNA silence bacterial genes?
FAQ ID -395
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How should I reconstitute the lyophilized RNase-Free DNase Set with the RNeasy 96 kit?
FAQ ID -3003
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Is it possible to use a standard processor — the kind used routinely for formalin-fixed samples — for dehydration and paraffin infiltration of PAXgene Tissue treated samples?
FAQ ID -3032
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Can I use Tungsten Carbide beads for RNA extraction protocols using QIAGEN Kits?
FAQ ID -3053
表示
Where can I find the ordering information for QIAcube accessories such as Shaker Rack plugs, Rack labeling strips, Reagent bottle rack, 30mL Reagent bottles, Rotor Adapter holder, Rotor adapters, Sample tubes CB, Sample tubes RB and Spin column adapter rings?
FAQ ID -3054
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What is the part number for O-rings for QIAsymphony SP and AS instruments? How often should the O-rings be replaced?
FAQ ID -3055
表示
What is the thermal output for a BioRobot MDx and BioRobot Universal?
FAQ ID -3056
表示
What is the thermal output for a QIAsymphony SP and AS instrument?
FAQ ID -3057
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How precise is the QIAgility?
FAQ ID -3063
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What are the advantages and disadvantages of turning on the tip “re-use” feature on the QIAgility?
FAQ ID -3064
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How long does it take to set up a 96-well plate PCR reaction on the QIAgility?
FAQ ID -3066
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Can I use a bar code scanner or reader on the QIAgility?
FAQ ID -3067
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How can I find the run parameters for a BioSprint protocol that I am running?
FAQ ID -3069
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Can BioSprint 96 be connected to LIMS?
FAQ ID -3070
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What is the expected level of endotoxins in plasmid DNA purified with QIAprep spin miniprep kit?
FAQ ID -3081
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What is the expected level of endotoxins in plasmid DNA purified with QIAGEN Plasmid kits, QIAfilter Plasmid kits and HiSpeed Plasmid purification kits?
FAQ ID -3082
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What is the concentration of the Gentra RNase A that is used with the Autopure and Puregene protocols?
FAQ ID -3083
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What is the concentration of the different Proteinase K solutions sold by QIAGEN?
FAQ ID -3084
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Where can I access Material Safety Data Sheets (MSDS) online for detailed information on the reagents for each respective kit?
FAQ ID -3085
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What tubes can be used with TissueLyser Adapter Set 2 x 96 (cat. no. 69984)?
FAQ ID -3086
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How to upload a Flexiplate on QIAGEN Webpage?
FAQ ID -3103
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Can we do modification XXXXX for custom siRNA that is not on the web page?
FAQ ID -3107
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What is the stability of siRNA lyophilized and resuspended?
FAQ ID -3109
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Do you offer FlexiTube or FlexiPlate siRNAs for rat?
FAQ ID -3114
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Is it possible to extract RNA from frozen blood?
FAQ ID -3119
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Is it possible to extract RNA from RNAprotect-stabilized-blood?
FAQ ID -3120
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What's the pulsed-field gel electrophoresis (PFGE) conditions of the gel picture showing on your website? http://www.qiagen.com/Search/MagAttract-HMW-DNA-Kit#productdetails
-48
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Can Dithiothreitol (DTT) be used instead of BME in Buffer RLT Plus of RNeasy Plus Mini Kit?
FAQ ID -3125
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Why does my purified DNA/RNA sometimes have a 260/280 or 260/230 ratio of more than 2? Does that mean the purity is poor?
FAQ ID -3132
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How do I remove the RNA contamination from purified DNA?
FAQ ID -3133
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What is the final concentration of Protease upon reconstitution in the QIAamp DNA Blood Mini?
FAQ ID -3140
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What is the Spike-in-Control in the miRNeasy Serum/Plasma Kit ?
FAQ ID -3169
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What is the difference between the 1 nmol FlexiTube and FlexiTube Gene Solution siRNAs?
FAQ ID -3174
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What could be a reason for cloudy precipitate in PCR reaction with STR Plus chemistry after cycling protocol is completed?
FAQ ID -3175
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What is needed for performing delta delta Ct relative quantitation on the Rotor-Gene Q?
FAQ ID -3178
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Is REST software Windows 7 compatible?
FAQ ID -3182
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Can the Rotor-Gene Q perform gradient PCR?
FAQ ID -3183
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What is the expected amplicon size of the Microbial DNA qPCR Assays?
FAQ ID — 3396
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What is the difference between Positive PCR Control (PPC) and Microbial DNA Positive Control?
FAQ ID — 3397
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What is LLOQ?
FAQ ID — 3401
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What is the difference between LLOQ and LOD?
FAQ ID — 3402
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What species are detected by the Pan Bacteria 1 and Pan Bacteria 3 Assays?
FAQ ID - 3427
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What is the composition of Buffer AC in the QIAamp UltraSens Virus Kit?
FAQ ID - 3429
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Can the miScript II RT Kit be used to quantify plant miRNAs?
FAQ ID - 3431
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What is the dissociation curve temperature of PCR products generated with the miScript Plant qPCR system?
FAQ ID - 3444
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Can specific types of white blood cells be enriched from a PAXgene Blood RNA Tube prior to the RNA isolation?
FAQ ID - 3467
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What is the proper disposal procedure for waste from the sample preparation?
FAQ ID - 3470
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What is the expected yield from 8.5 ml of blood?
FAQ ID - 3496
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What does the resuspension buffer, Buffer BG4, in the PAXgene Blood DNA kit contain?
FAQ ID - 3501
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How should blood samples drawn into PAXgene Blood DNA Tubes be transported?
FAQ ID - 3507
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How long can samples in PAXgene Blood DNA Tubes be stored at room temperature?
FAQ ID - 3508
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What is the expected DNA yield from 2.5 ml of blood when using the QIAsymphony, QIAcube, and salting-out precipitation method?
FAQ ID - 3510
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Which downstream applications have been tested with DNA purified from samples collected in PAXgene Blood DNA Tubes IVD?
FAQ ID - 3512
表示
What does PAXgene Tissue STABILIZER contain?
FAQ ID - 3513
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What is the minimum number of cells that can be efficiently processed with the QIAamp DNA Mini and QIAamp Blood Mini kits and what is the expected yield?
FAQ ID - 3516
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Is the quality and size of DNA extracted with the DNeasy Blood & Tissue kit good enough to generate DNA-libraries for next generation sequencing?
FAQ ID - 3517
表示
What is the minimum number of cells or minimum amount of tissue that can be efficiently processed with the RNeasy mini kit?
FAQ ID - 3519
表示
Can I use the RNeasy Fibrous Tissue Mini Kit (cat. no. 74704) to extract RNA from fibrous plant material?
FAQ ID - 3521
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Will the Reverse transcription control on the RT2 profiler PCR array work on any cDNA library?
FAQ ID - 3534
表示
Microscopic/visual confirmation of successfully sorted cells can be used to optimize sorting conditions. Can stained cells be used?
FAQ ID - 3559
表示
Is the miRNA reverse transcription control (miRTC) used in conjunction with the miScript Single Cell qPCR Kit?
FAQ ID - 3573
表示
Is clot detection possible on the QIAsymphony?
FAQ - ID 3588
表示
How can I determine if a tube is suitable for clot detection on QIAsymphony?
FAQ ID - 3590
表示
How should I thaw frozen plasma samples?
FAQ ID - 3645
表示
How do Unique Molecular Indexes (UMIs) improve quantification?
FAQ ID - 3669
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Can REPLI-g WGA be used to amplify cDNA if the cDNA is dsDNA (double-stranded DNA)?
FAQ ID - 3686
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I would like to stop during the library preparation procedure. When can I do that?
FAQ ID - 3687
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Which regions are covered by the GR DNAseq V2 Panels (#181900)?
FAQ ID - 3688
表示
When preparing plasma with the PAXgene Blood ccfDNA tubes, cat. # 768115, do you recommend that the first centrifugation step should be done with the brakes on or off?
FAQ ID - 3690
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How do I insert and replace an absorber strip into the PyroMark Q48 Autoprep chamber?
FAQ ID - 3691
表示
Are peak heights of Q48 comparable to other PyroMark instruments?
FAQ ID - 3692
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How much space does the PyroMark Q48 Autoprep instrument need?
FAQ ID - 3693
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Can unused wells in a pyrosequencing discs be used in the next run?
FAQ ID - 3694
表示
Where can I find the certificate of calibration for the Rotor-Disc OTV Kit (catalog number 981400)?
FAQ ID - 3695
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What is the minimum guaranteed shelf-life of the PAXgene Blood ccfDNA Tubes (100) (catalog no. 768115)?
FAQ ID - 3696
表示
What methods are used during normalization of RNAseq data in the secondary GeneGlobe Data Analysis Center?
FAQ ID - 3698
表示
How do I prepare Buffer MP?
FAQ ID - 3620
表示
Are the QIAshredder columns included in various QIAGEN kits the same?
FAQ ID - 3624
表示
What is the composition of buffer QBT?
FAQ ID -411
表示
What is the composition of buffer QC?
FAQ ID -412
表示
What is the composition of buffer QF?
FAQ ID -413
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What is the composition of buffer STE?
FAQ ID -415
表示
What is the composition of buffer TE?
FAQ ID -416
表示
What is the composition of buffer FWB2?
FAQ ID -417
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What is the composition of buffer P3?
FAQ ID -418
表示
What is the size, charge and isoelectric point of the DHFR protein in the pQE vectors?
FAQ ID -470
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Why is carrier RNA used during the isolation of gDNA from microdissected samples with the QIAamp DNA Micro Kit?
FAQ ID -473
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Why are the centrifugation speeds for the QIAamp DNA Mini kit at 6000 x g? Can I spin at full speed?
FAQ ID -474
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Are HEPES, MOPS and PIPES buffers compatible with QIAGEN's PhosphoProtein Purification kit?
FAQ ID -482
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Can Ni-NTA resins be used to purify protein with an internal His-tag?
FAQ ID -496
表示
How do I calculate the percentage of silencing with real-time RT-PCR for siRNA?
FAQ ID -498
表示
Do you have a protocol for the removal of endotoxins from already purified plasmid DNA?
FAQ ID -500
表示
Do you have stability data for genomic DNA isolated with the QIAamp DNA Blood Mini Kit?
FAQ ID -518
表示
What is the composition of the siRNA resuspension & annealing buffer?
FAQ ID -522
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Can Taq DNA Polymerase use RNA as a template, and generate false positives in "no-RT" controls?
FAQ ID -523
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What is Tissue-Tek O.C.T., and what is it used for?
FAQ ID -530
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Why do replicates in real-time PCR have different plateau heights?
FAQ ID -539
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How can I avoid primer-dimer formation during PCR amplification?
FAQ ID -544
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How can I tell if I have primer-dimers in my PCR reaction?
FAQ ID -552
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How should I store cDNA produced using Omniscript Reverse Transcriptase?
FAQ ID -561
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Is it possible to isolate DNA from bone marrow with the QIAamp DNA Blood Kits?
FAQ ID -563
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What is the composition of Buffer ER? Is it available separately?
FAQ ID -571
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What can I do when the DNA pellet prepared with QIAGEN Plasmid Kits has been overdried?
FAQ ID -572
表示
Do I have to remove the oil from my PCR reaction before using the QIAquick or MinElute PCR Purification Kit?
FAQ ID -575
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Are the columns of the QIAquick PCR Purification-, Gel Extraction-, and Nucleotide Removal Kit interchangeable?
FAQ ID -577
表示
What size is the smallest protein that can be synthesized with the EasyXpress Protein Synthesis Kit?
FAQ ID -600
表示
Why do I sometimes get light blue colonies when using the QIAGEN PCR Cloning Kit?
FAQ ID -603
表示
What do you recommend for the cleanup of genomic DNA (gDNA)?
FAQ ID -618
表示
How can I improve my RNA yield from liver sample when using RNeasy Kits?
FAQ ID -623
表示
Why do you recommend using Triton X for the purification of 6xHis-tagged protein?
-100
表示
What 96-well plates do you recommend for use with the LiquiChip Workstation?
FAQ ID -630
表示
What is a QIAshredder? Is it sufficient for complete disruption and homogenization of my tissue sample?
FAQ ID -631
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Why does the QIAamp DNA Mini Tissue Protocol require both ATL and AL buffer, while the Blood Protocol only uses AL?
FAQ ID -633
表示
Will the QIAquick PCR Purification Kit remove sufficient SYBR Green from real-time PCR reactions to allow sequencing?
FAQ ID -637
表示
What is the shelf-life of my QIAGEN Kit?
FAQ ID -651
表示
What are the differences between MDA and DOP/PEP methods of Whole Genome Amplification?
FAQ ID -665
表示
Can I purchase Phi29 DNA polymerase only?
FAQ ID -708
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What is the average DNA concentration obtained using the DirectPrep 96 Miniprep Kit?
FAQ ID -721
表示
I accidentally stored Buffer RDD of the RNase-Free DNase Set at°C. Will it still function?
-20
表示
I ran my RNA out on an agarose gel and can see lots of bands similar to a ladder. Why?
FAQ ID -745
表示
How much DNA is obtained in the average PCR reaction?
FAQ ID -750
表示
Do you have information about the cleanup of single-stranded DNA (ssDNA) with QIAquick columns?
FAQ ID -759
表示
How can I get a certificate for quality assurance (ISO 13485 and ISO 9001) from QIAGEN?
FAQ ID -762
表示
What is the difference between Ni-NTA Agarose and Ni-NTA Superflow?
FAQ ID -764
表示
What is the composition of Buffer N3?
FAQ ID -767
表示
Are the protocols from the BioSprint software compatible with the KingFisher software and vice versa?
FAQ ID -770
表示
How should fluorescent labeled probes be stored?
FAQ ID -784
表示
Is it possible to use the QuantiTect Reverse Transcription Kit with bacterial RNA?
FAQ ID -785
表示
Are Buffer PB of the QIAquick PCR Purification Kit and Buffer QG of the QIAquick Gel Extraction Kit interchangeable?
FAQ ID -786
表示
How can I get specific information and a quote for my individual Sequencing Service needs?
FAQ ID -792
表示
Can the QIAprep Spin Miniprep Kit be used for isolating plasmid DNA from mammalian cells?
FAQ ID -795
表示
How can I separate PCR fragments that are small and very close in size on an agarose gel?
FAQ ID -800
表示
Can I reuse the Ni-NTA Agarose and Ni-NTA Superflow resins?
FAQ ID -802
表示
What Disinfectant Solution do you recommend for the BioRobot MDx?
FAQ ID -809
表示
Is the E. coli Host Strain M15[pREP4] resistant to Zeocin?
FAQ ID -842
表示
What annealing temperature should be used with the QuantiTect Primer Assays?
FAQ ID -849
表示
Why is it recommended to add 1 mM IPTG for optimal protein yields using the EasyXpress Protein Synthesis Kits?
FAQ ID -860
表示
Which QIAGEN plasmid preparation kits will contain LyseBlue Reagent?
FAQ ID -865
表示
Do you have an in vitro translation kit allowing the incorporation of seleno-methionine for X-Ray crystallography based protein analysis?
FAQ ID -879
表示
Do you have a protocol for the isolation of genomic DNA from frozen clotted blood?
FAQ ID -900. Test
表示
Do you have protocols for the isolation of genomic DNA from tissue using QIAGEN-tips 2500 (Mega) and 10000 (Giga)?
FAQ ID -907
表示
Do you have a protocol for the isolation of genomic DNA from bone?
FAQ ID -908
表示
What do you suggest to prevent degradation of RNA isolated from tissue with high amounts of RNases using RNeasy?
FAQ ID -942
表示
Do you have a protocol for Cyanine 570, Cyanine 670, or biotin labeling of cDNA?
FAQ ID -959
表示
Do you have a protocol for reverse transfection of adherent cells with siRNA in 384-well plates?
FAQ ID -971
表示
Do you have a protocol for the purification of PCR products using the BioSprint System?
FAQ ID -984
表示
Do you have a protocol for transient transfection of Hela-S3 cells using PolyFect Transfection Reagent?
FAQ ID -997
表示
How can I analyze proteins from exosomes and other extracellular vesicles (EVs) obtained with the exoEasy Maxi Kit by SDS-PAGE?
FAQ ID - 3707
表示
How can I increase expression of my 6xHis-tagged protein in E. coli?
FAQ ID -63
表示
Can miRNA and other RNAs smaller than 200 nucleotides be isolated with the AllPrep DNA/mRNA Nano Kit?
148723
表示
What is the minimum amount of starting material that can be used with the DNA/mRNA Nano Kit?
148724
表示
What is the composition of buffer OW2?
FAQ ID -419
表示
What is the composition of buffer OBB?
FAQ ID -421
表示
Do I need to buy special kits for the QIAcube Connect MDx?
148725
表示
What applications are offered on the QIAcube Connect MDx instrument?
148726
表示
Can I program my own protocols for the QIAcube Connect MDx?
148727
表示
Can purification columns from other suppliers be processed on the QIAcube Connect MDx?
148728
表示
What are the dimensions and weight of the QIAcube Connect MDx?
148729
表示
Can the QIAcube rotor adapters be autoclaved?
148730
表示
Can the QIAcube rotor and/or buckets be removed for cleaning?
148731
表示
Can the QIAcube be connected to a laboratory information management system?
148732
表示
Are run reports and/or log files available on the QIAcube?
148733
表示
How can I get software updates for the QIAcube Connect MDx?
148734
表示
Can QIAcube Connect MDx protocol runs be interrupted, and subsequently be continued to completion?
148735
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?
148736
表示
Do I need to discard partially used QIAcube tip racks?
148738
表示
How can I decontaminate the QIAcube Connect MDx system?
148739
表示
How can I load new protocols onto the QIAcube Connect MDx?
148740
表示
Can the QIAcube Connect MDx heater/shaker be used independently from protocol runs?
148741
表示
Can the QIAcube Connect MDx centrifuge be used independently from protocol runs?
148742
表示
What dedicated QIAcube Kits are available?
148743
表示
Can I ask QIAGEN to upgrade my current QIAcube Connect Life Science instrument to make it an MDx instrument?
148744
表示
Can I run life science and custom protocols on a QIAcube Connect MDx?
148745
表示
What are the heating/cooling rates in the QIAquant instruments?
153919
表示
Is a passive internal reference dye, like ROX, required on the QIAquant to obtain reproducible results?
153920
表示
What sample volume is suitable for use in the QIAquant?
153921
表示
What types of reaction vessels are required for use in the QIAquant?
153922
表示
Is the QIAquant equipped with a temperature gradient function?
153923
表示
Are the 96- and 384-sample blocks interchangeable?
153924
表示
Is it possible to use the touch down PCR option on QIAquant with two acquisition points in the same channel?
153925
表示
How many molecules can be detected in the system?
153926
表示
What applications can the QIAquant be used for?
153927
表示
Can I upgrade my QIAquant 96 2plex instrument to QIAquant 96 5plex or modify the set of color channels?
153928
表示
Does QIAGEN offers arrays and assays configured specifically for QIAquant instrument?
153929
表示
Is the software of the QIAquant compatible with 21CFR part11?
153930
表示
Is it possible to import a standard curve from a previous run?
153947
表示
Can data be analyzed while the run is proceeding? Can data be analyzed from a previous experiment while another experiment is running?
153948
表示
Can I use QIAquant 96 Software to analyze experiments carried out on QIAquant 384?
153950
表示
Can I operate QIAquant 96 instrument using touchscreen and computer simultaneously?
153951
表示
Is it possible to establish an internet connection with QIAquant instrument?
153952
表示
Can I connect more than one QIAquant instrument to the same computer?
153953
表示
What is the algorithm behind data normalization in the QIAquant Software?
153954
表示
Is it possible to edit the sample sheet after the run in the QIAquant Software?
153955
表示
What are the LIMS capacity of the software?
153949
表示
Does the QIAquant Software have the capacity to export data? Which data formats can be used for the export?
153946
表示
I received a kit containing the MinElute columns; however, they were left out for a while and not stored at 2–8°C upon receipt. Can I still use them?
FAQ ID - 3560
表示
Is the DNA extracted with the QIAamp DNA FFPE Advanced Kits suitable for downstream applications that require more intact DNA such as long range PCR (>1 kb) and long read DNA sequencing?
153891
表示
What are recommended stopping points in the procedure of the QIAamp DNA FFPE Advanced Kits?
153892
表示
Can samples be lysed overnight with Proteinase K in the QIAamp DNA FFPE Advanced procedure?
153893
表示
Can the second Proteinase K lysis step in the QIAamp DNA FFPE Advanced procedure be carried out at lower temperatures than 65°C?
153894
表示
Can the 2nd Prot K step be omitted?
153896
表示
What size of DNA can be expected?
153897
表示
What is the difference of buffer FTB versus Buffer ATL?
153895
表示
Is it possible to change voltage set-up from 110V to 230V on the QIAcuity instruments?
3761
表示
How can I upgrade the software on the instrument (CSW) and the QIAcuity Software Suite?
3762
表示
Can I see error codes on the instrument touchscreen?
3763
表示
How are results stored within the QIAcuity Software Suite?
3764
表示
What is the scope of a regular maintenance of the QIAcuity?
3765
表示
Can the QIAcuity One 2plex be upgrade to the QIAcuity One 5plex?
3766
表示
Can I use an empty nanoplate without seal to perform a dry run?
3767
表示
Does an incorrect handling of a plate might affect the results?
3768
表示
What is the impact of not applying the latest VPF? Can I reanalyze previously obtained results after installing the latest VPF?
3769
表示
Can I see on the QIAcuity Software Suite report file if the VPF (Volume Precision Factor) has been used or not?
3770
表示
Is it necessary to reanalyze a plate with VPF (Volume Precision Factor) that was already processed using a QIAcuity instrument that was purchased in 2020?
3771
表示
How can I get the latest VPF (Volume Precision Factor)?
3772
表示
Where can I find assays specifically designed for QIAcuity?
3773
表示
Can I prepare a dPCR reaction directly in QIAcuity Nanoplate?
3774
表示
Can I use the dPCR master mix in a qPCR cycler for optimization purposes?
3775
表示
What is the purpose of the reference channel in QIAcuity?
3776
表示
How to prepare DNA prior to dPCR?
3778
表示
Can I use a custom master mix instead of a QIAGEN master mix?
3777
表示
Which sample preparation method is recommended for QIAcuity dPCR?
3779
表示
What are the storage conditions and expiry date of QIAcuity consumables?
3780
表示
What is the input volume for QIAcuity Nanoplate well?
3782
表示
Can I use the QIAcuity Nanoplate in more than one runs?
3781
表示
What is the VPF (Volume Precision Factor)?
3784
表示
When and how often do I need a new VPF (Volume Precision Factor)?
3785
表示
Is a standard curve needed in dPCR?
3786
表示
Which database versions are used for CRISPR-Q Custom PCR Assay and CRISPR-Q Sanger Primers design?
3788
表示
Is there anything to consider when processing cultured cells on coated cultivation dishes? Are additional purification steps required to eliminate or reduce coating reagents such as Poly-L-Lysine?
3791
表示
Is there something to consider when working with transduced cells treated with Polybrene?
3790
表示
For sequencing application, does the lysate require purification?
3792
表示
Are the CRISPR-Q PCR Assays and the CRISPR-Q Sanger Primers on GeneGlobe validated?
3793
表示
Are the PCR products generated with CRISPR-Q Custom PCR Assays only applicable to analysis of editing efficiency by Sanger sequencing?
3794
表示
Can the new CRISPR PCR Assays be used for dPCR on the QIAcuity? Do you have data or a protocol?
3795
表示
What is the minimum cell number needed for cell lysis?
3789
表示
For the Sanger analysis tool, the customer needs to upload two .abi1 files of forward and reverse sequences? Is there any additional info that needs to be provided?
3796
表示
What is the sequence of the QIAseq miRNA NGS 5’ Adapter?
FAQ ID - 3672
表示
What are recommended stopping points in the procedure of the EZ1&2 DNA FFPE Kits?
3753
表示
Are there other options for paraffin removal?
3754
表示
Can samples be lysed overnight with Proteinase K in the EZ1&2 DNA FFPE procedure?
3755
表示
Can the second Proteinase K lysis step in the EZ1&2 DNA FFPE procedure be carried out at lower temperatures than 65°C?
3756
表示
What is the difference between Buffer FTB and Buffer ATL?
3757
表示
Can the 2nd Proteinase K step be omitted?
3758
表示
What size of DNA can be expected?
3759
表示
Is the DNA extracted with the EZ1&2 DNA FFPE Kits suitable for downstream applications that require more intact DNA such as long-range PCR (>1 kb) and long-read DNA sequencing?
3760
表示
Do you recommend 1-step or 2-step real-time RT-PCR for gene expression analysis?
FAQ ID -1056
表示
3323 - Do you have a protocol for the AllPrep DNA/RNA/Protein Mini Kit on the QIAcube?
FAQ ID - 3323
表示
Does salt concentration in the food matter when using the DNeasy mericon Food Kit?
FAQ ID - 3346
表示
Why does the DNeasy mericon Food Kit use a QIAquick column and Buffer PB rather than a DNeasy column and Buffer AL, which might be expected since the kit isolates genomic DNA?
FAQ ID - 3347
表示
When would I use the mericon DNA Bacteria Kit vs the mericon DNA Bacteria Plus Kit?
FAQ ID - 3348
表示
Why is my 260/280 ratio low after using the DNeasy mericon Food Kit?
FAQ ID - 3349
表示
CAn I use milk or other liquids with the DNeasy mericon Food kit? What volume would I use?
FAQ ID - 3350
表示
What is the composition of QIAzol? What is the color of this reagent?
FAQ ID - 3355
表示
Is it possible to stop the DNeasy tissue protocol and store the tissue lysates after digesting in buffer ATL and Proteinase K?
FAQ ID - 3362
表示
I cannot analyze the data from your Investigator HID kits with my GeneMapper software. What can I do?
FAQ ID - 3363
表示
What is the QIAxcel QX RNA Size Marker 200-6000nt?
FAQ ID - 3365
表示
What is the nature of the gel in the QIAxcel RNA QC kit v2.0? Is it denaturing?
FAQ ID - 3366
表示
Do you sell CoralLoad dye separately?
FAQ ID - 3368
表示
Are QIAcube reagent bottles (cat. no. 990393) autoclavable? What type of plastic are they made of?
FAQ ID - 3369
表示
What is the composition of elution buffers used in QIAsymphony DNA Investigator kits?
FAQ ID - 3387
表示
Can I buy the RNeasy Mini columns, RNeasy MinElute columns, RNeasy Midi columns or the RNeasy Maxi columns separately?
FAQ ID - 3388
表示
Can I buy the gDNA eliminator plates supplied in your RNeasy Plus 96 kit separately?
FAQ ID - 3389
表示
Can I buy the gDNA eliminator columns supplied in your RNeasy Plus kits separately?
FAQ ID - 3390
表示
Why does AllPrep DNA/RNA/Protein Mini kit use buffer RLT, but Allprep DNA/RNA Mini and Allprep DNA/RNA Micro kits use buffer RLT Plus? Are these buffers interchangeable?
FAQ ID - 3391
表示
Do you have data to show lowest dropout rate with Repli-G WTA Single Cells kit?
FAQ ID - 3392
表示
What is the RNase A concentration and composition of Buffer P1?
FAQ ID -198
表示
Are protocols also available for other instruments (e.g., Hamilton Star and Tecan Fluent)?
3797
表示
Where can I download the protocol for the KingFisher Flex?
3798
表示
Who can help in case of issues with the third party instrument?
3799
表示
Is the virus inactivated during the procedure?
3800
表示
Can I use sample volumes other than 300 µl?
3801
表示
Who can help if it is not clear if issues are caused by the third party instrument or by the chemistry?
3802
表示
I would like to use the kit on another third party instrument. Who should I contact?
3803
表示
What are common sized libraries observed on a TapeStation, Bioanalyzer, or similar instruments?
FAQ ID - 3837
表示
Are the QIAseq miRNA NGS 5’ Adapter and QIAseq miRNA NGS RT Initiator compatible with the QIAseq miRNA UDI kits?
FAQ ID - 3836
表示
What is the sequence of the UDI 5' Adapter?
FAQ ID - 3835
表示
Can you perform qPCR analysis of miRNAs from libraries prepared with the QIAseq miRNA Library Kit?
FAQ ID - 3674
表示
What can be used to validate results obtained with the QIAseq miRNA Library Kit?
FAQ ID - 3675
表示
What is the maximum number of available sample indexes?
FAQ ID - 3665
表示
What are recommended stopping points during the QIAseq miRNA Library Kit procedure?
FAQ ID - 3663
表示
Should total RNA or small enriched RNA be used as the starting material for the QIAseq miRNA Library Kit?
FAQ ID - 3659
表示
What is the recommended read length for libraries prepared using the QIAseq miRNA Library Kit?
FAQ ID - 3668
表示
What is the acceptable number of reads per sample per miRNA sequencing run?
FAQ ID - 3673
表示
Do you have a protocol for the isolation of genomic DNA from whole blood for use in MRC-Holland MLPA® assays?
FAQ ID -1169
表示
Is training of lab personnel included with the purchase of a BioRobot EZ1?
FAQ ID -1239
表示
Do the foils sealing the EZ1 Reagent Cartridges have to be manually removed prior to loading the robot?
FAQ ID -1240
表示
How can we get our BioRobot EZ1 upgraded when new protocols are launched?
FAQ ID -1241
表示
Where can I find information about the worktable setup on the BioRobot EZ1?
FAQ ID -1243
表示
What disposables are required for nucleic acid isolations on the BioRobot EZ1?
FAQ ID -1246
表示
How should I prepare buffy coat samples for use on the BioRobot EZ1?
FAQ ID -1249
表示
Do you have a protocol for the isolation of DNA from buffy coat using the BioRobot EZ1?
FAQ ID -985
表示
What has to be done to an RNA sample before loading it onto an Agilent Bioanalyzer?
FAQ ID -528
表示
Do you have a protocol for the isolation of total nucleic acids from animal and human tissues on the BioRobot EZ1?
FAQ ID -975
表示
Do you have a protocol for the isolation of total RNA from paraffin-embedded sections on the BioRobot EZ1?
FAQ ID -976
表示
Do you have a protocol for the isolation of DNA from fungi using the BioRobot EZ1?
FAQ ID -992
表示
Are the new EZ1 RNA Kits (cat. no. 958034; 959034; 956034) compatible with the previous EZ1 RNA Card (cat. no. 9015590) or EZ1 RNA Universal Tissue Card (cat. no 9016384)?
FAQ ID -1025
表示
What are the advantages of EnzScript M-MLV Reverse Transcriptase RNase H-(P7600) versus wild type M-MLV Reverse Transcriptase (P7040)?
FAQ ID - 3838
表示
What types of priming are compatible with EnzScript M-MLV Reverse Transcriptase RNase-H-?
FAQ ID - 3839
表示
What is the optimal reaction temperature for EnzScript M-MLV Reverse Transcriptase RNase H-?
FAQ ID - 3840
表示
What PCR enzymes can be used following the first-strand synthesis?
FAQ ID - 3841
表示
What is the suggested protocol for generating long, full-length cDNA transcripts (>5 kb)?
FAQ ID - 3842
表示
What region of LINE gets targeted by the assay for PyroMark Q96 MD or PyroMark Q24?
2857
表示
Does the PyroMark LINE assay target all LINE sequences?
2860
表示
What is the amplicon length of the PyroMark CpG LINE assay?
2856
表示
How do I perform the PyroMark Q24 Advanced upgrade?
FAQ ID -3163
表示
Is it possible to use PyroMark Q24 Advanced reagents on PyroMark Q24 system?
FAQ ID -3160
表示
What are the differences between new PyroMark Q24 Advanced reagents chemistry and PyroMark Q24 Gold reagents?
FAQ ID -3165
表示
How accurate and reliable is PyroMark Q24 in mutation analysis?
FAQ ID -2094
表示
We recently changed the OS from Windows XP to Windows 7. When re-installing software Pyromark Q24 2.0.6, it fails to analyze the results. Any suggestions?
FAQ ID - 3621
表示
What is the use of the PyroMark Q24 Validation Oligo?
FAQ ID -2855
表示
How does the built-in QC control for complete bisulfite conversion of DNA work on PyroMark Q24?
FAQ ID -2095
表示
How long does a single run on the PyroMark Q24 take?
FAQ ID -2096
表示
3843-How-do-I-prevent-a-drifting-baseline-in-my-pyrosequencing-pyrogram
FAQ ID - 3843
表示
When do I have to change the pulse settings/methods in a pyrosequencing run setup?
FAQ ID -2942
表示
What is a PyroMark instrument method or instrument code?
FAQ ID -2941
表示
Can the PyroMark Q96 CpG LINE assay be used with an ID system?
2861
表示
How many times can the cartridges for PyroMark Q24 or PyroMark Q96 ID instruments be reused?
FAQ ID -2863
表示
How do I prevent a drifting baseline in my pyrosequencing pyrogram? If this method cannot be selected automatically in the application software, you can download the method/code file from the instrument webpage.
FAQ ID -2878
表示
Can unused wells in a pyrosequencing plate be used in the next run?
FAQ ID -2872
表示
What is the reason for signals ceasing in the middle of a pyrosequencing run?
FAQ ID -2875
表示
Is the CpG software included in the PyroMark instruments to study methylation status?
FAQ ID -2842
表示
What is the reason for split peaks appearing in between dispensations on my pyrosequencing pyrogram?
FAQ ID -2881
表示
Where can I find explanations to the warning given by the PyroMark software after run data analysis?
FAQ ID -2874
表示
Which heating block is recommended for the pyrosequencing annealing step?
FAQ ID -2838
表示
How many times can vacuum troughs be reused with the PyroMark Vacuum Preparation Stations?
FAQ ID -2848
表示
What kind of shaker should be used for the pyrosequencing binding step?
FAQ ID -2837
表示
What is the reason for a high substrate peak in the pyrosequencing pyrogram?
FAQ ID -2879
表示
How many CpG sites are analyzed by the PyroMark CpG LINE assay?
2858
表示
Is there a user manual available for the PyroMark Assay design software?
FAQ ID -2851
表示
Which operating system is compatible with PyroMark IdentiFire Software?
FAQ ID - 3340
表示
How do I set up a PyroMark CpG Assay?
FAQ ID -2814
表示
What is the purpose of the unmethylated and unconverted control DNA of the EpiTect PCR Control DNA Set?
FAQ ID -2007
表示
Will the primer sequence for the PyroMark CpG Assay be provided?
FAQ ID -2823
表示
Does QIAGEN offer a design of Custom PyroMark CpG Assays?
FAQ ID -2818
表示
How are the PyroMark CpG Assays reconstituted?
FAQ ID -2817
表示
How are the PyroMark CpG Assays shipped and stored?
FAQ ID -2816
表示
What are the features of PyroMark CpG Assays, for example, in terms of design and validation?
FAQ ID -2821
表示
What is included in a PyroMark Custom Assay?
FAQ ID -2815
表示
In which format can PyroMark CpG Assays be ordered?
FAQ ID -2824
表示
Which kits can be used in combination with the PyroMark CpG Assays and PyroMark Custom Assays?
FAQ ID -2822
表示
Does the PyroMark Assay Design or application software give any cycling conditions for individual assay primers or a PCR setup pipetting scheme?
FAQ ID -2862
表示
What is the recommended amplicon size for CpG assays?
FAQ ID -2825
表示
What kind of reading length can I expect when using pyrosequencing technology for sequence analysis?
FAQ ID -2216
表示
Will dUTP in a PCR reaction affect pyrosequencing?
FAQ ID -2843
表示
Which purity grade is recommended for pyrosequencing primers?
FAQ ID -2832
表示
What concentration should be used for the sequencing primer in pyrosequencing?
FAQ ID -2826
表示
What is the concentration of PyroMark Control Oligo?
FAQ ID -2846
表示
What is the sample throughput of pyrosequencing systems?
FAQ ID -2215
表示
How do I reduce background peaks in the pyrosequencing pyrogram?
FAQ ID -2877
表示
What is the sensitivity limitation for pyrosequencing?
FAQ ID -2840
表示
What should be the single peak height for the PyroMark Control Oligo on the different PyroMark instruments?
FAQ ID -2852
表示
Which end of the PCR primer for pyrosequencing should be biotinylated?
FAQ ID -2839
表示
How many nucleotides of a homopolymer can be resolved in pyrosequencing?
FAQ ID -2871
表示
Where can I order the Streptavidin Sepharose beads for pyrosequencing?
FAQ ID -2850
表示
What are critical steps during CTC enrichment?
3830
表示
How pure are the CTCs enriched from blood samples using the AdnaTest?
3831
表示
Can frozen blood be used for the procedure?
3832
表示
Can the EZ2 AdnaTest be used for other body fluids than blood?
3833
表示
Can Heparin blood be used?
3834
表示
Can the kit be used on the EZ2 Connect?
FAQ ID - 3845
表示
Can I use a different elution buffer?
FAQ ID - 3847
表示
What is the average amount of cfDNA present in 1 ml plasma?
FAQ ID - 3846
表示
Can the kit be used on the EZ1 Advanced XL?
FAQ ID - 3844
表示
Do you have a protocol for purification of cytoplasmic RNA from animal cells?
FAQ ID -1257
表示
What kits does QIAGEN offer to extract RNA from whole blood?
FAQ ID -304
表示
What is the composition of Buffer RLT?
FAQ ID -2793
表示
What is the key technical challenge in isolating high quality RNA from cell or tissue samples?
FAQ ID -2656
表示
Do you have a protocol for the isolation of RNA from leukocytes in milk?
FAQ ID -952
表示
What is the maximum binding capacity of RNeasy spin columns?
FAQ ID -290
表示
Can QIAquick Kits be used to clean up RNA samples?
FAQ ID -490
表示
Are RNeasy spin columns sold separately?
FAQ ID -159
表示
Can the RNase-Free DNase Set be used for DNase digestions of RNA in solution?
FAQ ID -619
表示
Which kit should be used to extract RNA from adipose tissue, brain, and other fatty animal tissues?
FAQ ID -467
表示
How can I minimize degradation of RNA from my pancreas sample?
FAQ ID -624
表示
What is the composition of Buffer RW1?
FAQ ID -2796
表示
Do you have a protocol for purification of total DNA from crude lysates?
FAQ ID -1255
表示
Do you have a protocol for isolation of genomic DNA from saliva and mouthwash?
FAQ ID -917
表示
Do you have a protocol for purification of total DNA from yeast?
FAQ ID -1253
表示
Do you have a protocol for the isolation of DNA from soft tissues using the TissueLyser?
FAQ ID -924
表示
Do you have a protocol for purification of total DNA from insects?
FAQ ID -1254
表示
What is the shelf-life for QIAGEN Proteinase K (cat. no. 19131, 19133)?
FAQ ID - 3447
表示
Do you have a protocol for the isolation of genomic DNA from sperm?
FAQ ID -909
表示
What is the advantage of running an analytical gel with fractions of my plasmid preparation?
FAQ ID -769
表示
What is the recipe for LB?
FAQ ID -212
表示
How do I know if my plasmid is a high- or low copy number type?
FAQ ID -350
表示
Can I eliminate RNase A from buffer P1 for my plasmid preparation to obtain RNase-free DNA for in-vitro transcription?
FAQ ID -366
表示
I left Buffer P1 at room temperature after addition of RNase A, what shall I do?
FAQ ID -859
表示
With LyseBlue reagent for lysis control, can I now process more bacterial culture and overload the columns?
FAQ ID -864
表示
What is the recipe for 2x YT?
FAQ ID -213
表示
What are the additional plasmid bands I see on my gel?
FAQ ID -1059
表示
Do you have a protocol for the isolation of plasmid DNA from Bacillus subtilis?
FAQ ID -896
表示
What is the composition of Buffer PB?
FAQ ID -2791
表示
Do you have a protocol for obtaining > 20 µg plasmid DNA using the QIAprep Spin Miniprep Kit?
FAQ ID -3102
表示
Why is my plasmid DNA yield low?
FAQ ID -768
表示
Why do I get genomic DNA contamination in my plasmid prep?
FAQ ID -353
表示
Do you have a protocol for the isolation of plasmid DNA from Agrobacterium?
FAQ ID -898
表示
I am seeing a precipitate after adding LyseBlue reagent to Buffer P1. What should I do about that?
FAQ ID -1045
表示
What to do if cell clumps are present after Buffer P2 addition when using LyseBlue Reagent?
FAQ ID -861
表示
What is the recipe for SOC medium?
FAQ ID -798
表示
How much RNA does a typical mammalian cell contain?
FAQ ID -2946
表示
Do I have to discard Buffer RLT with beta-Mercaptoethanol (ß-ME) added to it after 1 month of storage?
FAQ ID -1037
表示
What are the effects of low A260/A230 ratios in RNA preparations on downstream applications?
FAQ ID -2248
表示
Do I need to purchase any consumable for processing the kit on EZ2 Connect?
FAQ ID - 3849
表示
Are we able to customize protocol on the EZ2 Connect?
FAQ ID - 3850
表示
Which version of the EZ2 Connect can run the EZ2 RNA/miRNA Tissue/Cells Kit?
FAQ ID - 3851
表示
Can the kit be run on EZ1 instruments?
FAQ ID - 3852
表示
How can I check the integrity of RNA purified using RNeasy Kits?
FAQ ID -1024
表示
What are the limits of detection of the QIAxcel Connect?
FAQ ID - 3853
表示
Are all QIAxcel Cartridge Kits compatible with QIAxcel Connect?
FAQ ID - 3856
表示
What are the differences between QIAxcel Advanced and QIAxcel Connect?
FAQ ID - 3857
表示
What is the QIAxcel Connect System?
FAQ ID - 3859
表示
Can I combine your CGT dPCR assays with custom designed assays?
FAQ ID - 3861
表示
How many assays can be multiplexed?
FAQ ID - 3862
表示
In which channels can you detect the CGT dPCR assays?
FAQ ID - 3863
表示
How can I resuspend the lyophilized assay?
FAQ ID - 3864
表示
What quenchers are used?
FAQ ID - 3865
表示
Do I need to use restriction enzymes when quantifying AAV genomes?
FAQ ID - 3866
表示
Can the CGT dPCR assays also be used for the quantification of non-AAV samples?
FAQ ID - 3868
表示
Can I use the CGT dPCR assays for the titer determination of RNA viruses?
FAQ ID - 3869
表示
How do I know if the assays are compatible with the sample DNA of interest?
FAQ ID - 3870
表示
Are the assays also compatible with qPCR?
FAQ ID - 3871
表示
Can they be used with lentiviral vectors?
FAQ ID - 3872
表示
Is restriction enzyme digestion required?
FAQ ID - 3875
表示
dPCR results are in copies per microliter. How do I calculate host cell DNA contamination in femtogram per microliter?
FAQ ID - 3876
表示
My samples are highly fragmented. Is the dPCR result for resDNA quantification accurate?
FAQ ID - 3877
表示
Is dPCR sensitive to inhibition?
FAQ ID - 3880
表示
Is DNA extraction from the samples needed?
FAQ ID - 3873
表示
How much sample can I load for detecting host cell contamination?
FAQ ID - 3879
表示
Where can I find a copy of the .kpf file for a BioSprint protocol?
FAQ ID -3073
表示
Can the DyeEx 96 kit be used to clean sequencing reactions to be run on ABI 3730?
FAQ ID -3075
表示
What is the minimum number of samples that can be extracted on a BioSprint 96?
FAQ ID -3076
表示
Can the FastLane Cell lysates (containing stabilized RNA, step 8. in Fastlane protocol) be stored?
FAQ ID -3077
表示
Can I use specific primers with the FastLane Kits?
FAQ ID -3078
表示
Can the FastLane RT reaction be incubated longer than 30 min at 42 deg C?
FAQ ID -3079
表示
Does carrier RNA interfere with the QuantiTect Whole Transcriptome amplification?
FAQ ID -3080
表示
Which SARS-CoV-2 targets can the SARS-CoV-2 Neo Kit detect?
FAQ ID - 3881
表示
Do we have specificity and sensitivity data for this kit?
FAQ ID - 3882
表示
Do we have specificity and sensitivity data for this kit?
FAQ ID - 3883
表示
Is it possible to scale up sample volume and reaction volume?
FAQ ID - 3884
表示
What color channels are used?
FAQ ID - 3885
表示
What is the percentage of false negative results that QIAGEN obtained during validations?
FAQ ID - 3886
表示
What is the minimum and maximum concentration of effective RNA for the test?
FAQ ID - 3887
表示
Anything important when starting the cycler run?
FAQ ID - 3888
表示
Is it possible to use ABI instruments without ROX as a passive reference?
FAQ ID - 3889
表示
What is the shelf-life of the Neo Assay Kit?
FAQ ID - 3890
表示
Can the SARS-CoV-2 Neo Assay Kit detect all variants?
FAQ ID - 3891
表示
Why did we not choose commonly used genes such as the S gene, E gene, or RdRP?
FAQ ID - 3892
表示
Why did you choose ORF1a+ORF1b and ORF3a+ORF7a?
FAQ ID - 3893
表示
Can I use ROX as passive reference dye with the SARS-CoV-2 Neo assay?
FAQ ID - 3894
表示
Can I use the IC RNA of the QIAprep& Viral RNA UM Kit?
FAQ ID - 3895
表示
Which positive control should I use?
FAQ ID - 3896
表示
How long can eluates be stored after sample preparation using the EZ1 instruments or EZ2 Connect MDx and the EZ1 DSP Virus Kit?
FAQ ID - 3897
表示
How stable is Phoenix Hot Start Taq when incubated in a PCR reaction mix at room temperature?
FAQ ID - 3898
表示
How can PCR cycling conditions be optimized for Phoenix Hot Start Taq?
FAQ ID - 3899
表示
Can Phoenix Hot Start Taq utilize cDNA as template for PCR?
FAQ ID - 3900
表示
Is Phoenix Hot Start Taq capable of multiplex PCR?
FAQ ID - 3901
表示
How can I optimize Mg2+ conditions for a specific amplicon when using Phoenix Hot Start Taq and the supplied reaction buffer?
FAQ ID - 3902
表示
When should I use Phoenix Hot Start Taq GC reaction Buffer?
FAQ ID - 3903
表示
What is the amplification length limit of Phoenix Hot Start Taq?
FAQ ID - 3904
表示
What is the fidelity/error rate of Phoenix Hot Start Taq?
FAQ ID - 3905
表示
Why is the Phoenix Hot Start Taq sometimes cloudy upon removing from -20°C storage?
FAQ ID - 3906
表示
How can yield for long targets be increased when using Phoenix Hot Start Taq?
FAQ ID - 3907
表示
How is VeraSeq 2.0 DNA Polymerase different from the standard recombinant Taq-B DNA Polymerase?
FAQ ID - 3908
表示
How can I optimize Mg2+ conditions for a specific amplicon when using VeraSeq 2.0 DNA Polymerase and the supplied reaction buffers?
FAQ ID - 3909
表示
When should I use 5X VeraSeq GC Buffer?
FAQ ID - 3910
表示
What is the amplification length limit of VeraSeq 2.0 DNA Polymerase?
FAQ ID - 3911
表示
Why is VeraSeq 2.0 DNA Polymerase sometimes cloudy upon removing from -20°C storage?
FAQ ID - 3913
表示
What is the amplification length limit of VeraSeq 2.0 DNA Polymerase?
FAQ ID - 3912
表示
How can yield for targets be increased when using VeraSeq 2.0 DNA Polymerase?
FAQ ID - 3914
表示
Will VeraSeq 2.0 DNA Polymerase incorporate dUTP?
FAQ ID - 3915
表示
Is VeraSeq 2.0 DNA Polymerase available as a hot start enzyme?
FAQ ID - 3916
表示
How long can reaction components incubate with VeraSeq 2.0 DNA Polymerase at room temperature prior to PCR cycling?
FAQ ID - 3917
表示
What denaturation temperature should be used in cycling conditions?
FAQ ID - 3918
表示
What annealing temperature should be used in the cycling conditions?
FAQ ID - 3919
表示
What is the stability of VeraSeq 2.0 DNA Polymerase at room temperature?
FAQ ID - 3920
表示
How can I optimize Mg2+ conditions for a specific amplicon when using VeraSeq ULtra DNA Polymerase and the supplied reaction buffers?
FAQ ID - 3922
表示
How is VeraSeq ULtra DNA Polymerase different from the standard recombinant Taq-B DNA Polymerase?
FAQ ID - 3921
表示
When should I use 5X VeraSeq GC Buffer?
FAQ ID - 3923
表示
What is the amplification length limit of VeraSeq ULtra DNA Polymerase?
FAQ ID - 3924
表示
What is the fidelity/error rate of VeraSeq ULtra DNA Polymerase?
FAQ ID - 3925
表示
How can yield for targets be increased when using VeraSeq ULtra DNA Polymerase?
FAQ ID - 3926
表示
Will VeraSeq ULtra DNA Polymerase incorporate dUTP?
FAQ ID - 3927
表示
Do the DNA fragments generated by VeraSeq ULtra DNA Polymerase have a single-base 3´ overhang?
FAQ ID - 3928
表示
Is VeraSeq ULtra DNA Polymerase available as a hot start enzyme?
FAQ ID - 3929
表示
What denaturation temperature should be used in the cycling conditions?
FAQ ID - 3931
表示
What annealing temperature should be used in the cycling conditions?
FAQ ID - 3932
表示
What are the ResDNA Quant Kit components?
FAQ ID - 3878
表示
How can I load new protocols onto the QIAcube?
FAQ ID -1421
表示
Are run reports and/or log files available on the QIAcube?
FAQ ID -1412
表示
What applications are offered on the QIAcube?
FAQ ID -1403
表示
Can the QIAcube heater/shaker be used independently from protocol runs?
FAQ ID -1422
表示
What EZ1 DNA Investigator protocol is recommended for very precious samples?
FAQ ID -1154
表示
When should the Normalization protocol be used?
FAQ ID -1155
表示
What fluorescent labels are 6-FAM, BTG, BTY, BTR, and BTO in Matrix Standard BT5 single or multi.cap?
FAQ ID - 3364
表示
Does the EpiTect Hi-C Data Analysis Portal cost money?
FAQ ID -
143077
表示
What is the effect of using amounts of input material per sample that fall outside the recommended range?
FAQ ID -
143064
表示
What is the required amount of input material per sample for the EpiTect Hi-C Kit?
FAQ ID -
143063
表示
Does QIAGEN provide data analysis to accompany the EpiTect Hi-C Kit?
FAQ ID -
143075
表示
How can I extract DNA from a polyacrylamide (PAGE) gel?
FAQ ID -120
表示
Why does my DNA sample float out of the slot when loading it onto an agarose gel?
FAQ ID -205
表示
What is the small band below my fragment of interest on an agarose gel after DNA cleanup using QIAquick?
FAQ ID -148
表示
I bound an 11 kb DNA fragment to a QIAquick column; is it completely lost?
FAQ ID -756
表示
Is it possible to isolate single stranded DNA (ssDNA) with the QIAEX II Kit from agarose or polyacrylamide gels?
FAQ ID -576
表示
Can DNA yields be increased by prolonging incubation with proteinase K in Buffer ATL?
FAQ ID -2032
表示
Can the QIAcube be connected to a laboratory information management system?
FAQ ID -1411
表示
What are the dimensions and weight of the QIAcube?
FAQ ID -1407
表示
What dedicated QIAcube Kits are available?
FAQ ID -2337
表示
How can I decontaminate the QIAcube system?
FAQ ID -1419
表示
Can the QIAcube rotor and/or buckets be removed for cleaning?
FAQ ID -1410
表示
Can the QIAcube centrifuge be used independently from protocol runs?
FAQ ID -1423
表示
Do I need to buy special kits for the QIAcube?
FAQ ID -1402
表示
Do I need to discard partially used QIAcube tip racks?
FAQ ID -1418
表示
Can I program my own protocols for the QIAcube?
FAQ ID -1405
表示
Can the CGT dPCR assays also be used for the analysis of AAV genome integrity?
FAQ ID - 3867
表示
Is the QIAprep& CRISPR Kit also applicable to other gene-editing technologies such as TALENs and ZFN?
3787
表示
Do you have a protocol for the isolation of viral RNA from stool?
FAQ ID -918
表示
Which extraction kits are recommended?
FAQ ID - 3874
表示
How long can I store the reconsituted assay regarding QIAcuity HEK293 resDNA Quant Kit (96) at 4°C?
FAQ ID - 3934
表示
What is the preferred storage temperature for reconstituted assay for the QIAcuity HEK293 resDNA Quant Kit (96)?
FAQ ID - 3935
表示
What is the amount of standard for the different kit?
FAQ ID - 3936
表示
How did you calculate the conversion factor?
FAQ ID - 3937
表示
What does the standard kit contain?
FAQ ID - 3938
表示
What region is targeted in the QIAcuity E. coli resDNA Quant Kit (96)?
FAQ ID - 3939
表示
How long are sample lysates stable in the fridge/ freezer?
FAQ ID -
143765
表示
Can solid samples be processed with the QIAsymphony DNA Investigator Kit on the instrument?
FAQ ID -2027
表示
Should sample lysate volumes be exactly 200 µL, 500 µL, or 1000 µL when loaded on the QIAsymphony SP?
FAQ ID -2031
表示
After bisulfite conversion, can the DNA be stored?
FAQ ID -2409
表示
Which version of the EZ2 Connect can run the EZ2 RNA FFPE Kit?
FAQ ID - 3940
表示
When should I use the standard vs. the fast protocol for the EZ2 RNA FFPE Kit?
FAQ ID - 3941
表示
What size of RNA can be expected?
FAQ ID - 3942
表示
Which version of the EZ2 Connect can run the EZ2 AllPrep DNA/RNA FFPE Kit?
FAQ ID - 3947
表示
When should I use the ‘Standard’ vs. the ‘Fast’ protocol for the EZ2 AllPrep DNA/RNA Kit
FAQ ID - 3948
表示
Are there other options for paraffin removal?
FAQ ID - 3949
表示
What are recommended stopping points in the procedure of the EZ2 AllPrep DNA/RNA FFPE Kit?
FAQ ID - 3950
表示
Why is there a need to overlay the resuspended DNA pellet with PRS again (step 17 of QSP)?
FAQ ID - 3951
表示
An immediate subsequent AllPrep DNA/RNA FFPE run does not start right away.
FAQ ID - 3952
表示
Can I use the EZ2 AllPrep DNA/RNA FFPE kit to extract DNA/RNA from fresh frozen tissue?
FAQ ID - 3953
表示
What size of RNA can be expected?
FAQ ID - 3954
表示
Are there specific recommendations for performing RT-PCR on RNA isolated from paraffin-embedded samples?
FAQ ID - 3955
表示
My overall RNA yield is fine but RT-PCR performance poor – how can I improve this?
FAQ ID - 3956
表示
Why are my DV200 values of my RNA sample so low?
FAQ ID - 3957
表示
The integrity of my DNA sample (e.g. QIAxcel Connect) is bad.
FAQ ID - 3958
表示
How do I proceed if the amount of starting material cannot be calculated in detail?
FAQ ID - 3943
表示
Are there other options for paraffin removal?
FAQ ID - 3946
表示
Are there specific recommendations for performing RT-PCR on RNA isolated from paraffin-embedded samples?
FAQ ID - 3944
表示
My overall RNA yield is fine but RT-PCR performance poor – how can I improve this?
FAQ ID - 3945
表示
Is this available without glycerol?
FAQ ID - 3959
表示
What types of priming are compatible with EnzScript M-MLV RT RNase H-?
FAQ ID - 3961
表示
What is the suggested protocol for generating long, full-length cDNA transcripts (> 5 kB)?
FAQ ID - 3964
表示
What are the advantages of EnzScript M-MLV Reverse Transcriptase RNase H- (P7600) versus wild type M-MLV Reverse Transcriptase (P7040)?
FAQ ID - 3960
表示
What PCR enzymes can be used following first-strand synthesis?
FAQ ID - 3963
表示
Is the kit compatible with unpurified in-process samples?
FAQ ID - 3965
表示
Do I need to use Proteinase K in the CGT Viral Vector Lysis Kit? What is the recommended concentration?
FAQ ID - 3971
表示
Do you recommend storage of highly diluted AAV samples?
FAQ ID - 3972
表示
Is it possible to store the lysates? How can the lysates be stored?
FAQ ID - 3973
表示
Can I use MspI or HpaII restriction enzymes from other suppliers?
FAQ ID - 3975
表示
How many AAV genome copies can I load into the QIAcuity?
FAQ ID - 3977
表示
Do you need to dilute the lysates before setting up the PCR mix?
FAQ ID - 3978
表示
How do I know if the CGT dPCR assays are compatible with the sample DNA of interest?
FAQ ID - 3980
表示
Are the CGT dPCR assays also compatible with qPCR?
FAQ ID - 3981
表示
Can the CGT Viral Vector Lysis kit be used with assays of other suppliers or custom designed assays?
FAQ ID - 3982
表示
What is included in the SureSilencing shRNA Plasmids shipment?
FAQ ID -2785
表示
Is the QIAxcel Advanced discontinued?
FAQ ID - 3983
表示
What is the concentration range for RNA Integrity Score analysis when using the QIAxcel RNA High Sensitivity Kit?
FAQ ID - 3984
表示
What effect does homogenization have on DNA yield and integrity when using QIAwave DNA/RNA Kits?
FAQ ID - 3985
表示
What water should I use to prepare the buffer concentrates?
FAQ ID - 3986
表示
What is the new Waste Tube made of?
FAQ ID - 3987
表示
Are the QIAwave kits based on a different chemistry than the legacy kits?
FAQ ID - 3990
表示
Is there a way to compare the environmental impacts of the kit?
FAQ ID - 3991
表示
Can the QIAwave kits be recycled?
FAQ ID - 3992
表示
Does the reuse of the Waste Tubes increase the risk of cross-contamination?
FAQ ID - 3988
表示
I don’t have any glassware in the lab, is the QIAwave kit still a good option for me?
FAQ ID - 3989
表示
Is the Reagent Bottle Rack, Grey, QC2 (cat. no. 9026197) compatible with the QIAcube Classic instrument?
FAQ ID - 3993
表示
Is the kit compatible with unpurified in-process samples?
FAQ ID - 3994
表示
My samples are expected to have low concentrations. Can I load more sample into the workflow or more lysate into the PCR reaction?
FAQ ID - 3995
表示
Can I use Internal Control as overall control?
FAQ ID - 3996
表示
How long can I store the reconstituted Internal Control and the reconstituted Positive Control?
FAQ ID - 3997
表示
Do you recommend storage of highly diluted mycoplasma samples?
FAQ ID - 3998
表示
What are the major differences between QIAseq Targeted RNA Panel TCR kit and previous QIAseq Immune Repertoire RNA library kit?
FAQ ID - 3999
表示
On which instrumentation will the RT² Profiler PCR Array work?
FAQ ID -2719
表示
Investigator Quantiplex: Which version of the Applied Biosystems 7500 Real-Time PCR System software can be used to run the Investigator Quantiplex?
FAQ ID -2569
表示
Investigator Quantiplex: Do I have to calibrate new dyes on my Applied Biosystems 7500 or 7500 Fast Real-Time PCR System?
FAQ ID -2571
表示
Which human target is used for the quantification in the Investigator Quantiplex Kit?
FAQ ID -2577
表示
Investigator Quantiplex Pro: On which real-time cyclers is the Investigator Quantiplex Pro Kit validated?
FAQ ID - 3728
表示
Investigator Quantiplex and Quantiplex Pro: What do I have to consider if I am using Applied Biosystems SDS software version 1.2.3?
FAQ ID -2570
表示
Investigator Quantiplex Pro: Which real-time cycler software version can be used to run the kit?
FAQ ID - 3730
表示
Investigator Quantiplex Pro RGQ: Which real-time cycler software version can be used to run the kit?
FAQ ID - 3743
表示
Investigator Quantiplex Pro RGQ: Which Rotor-Gene Q System can be used to run the kit?
FAQ ID - 3742
表示
Investigator Quantiplex Pro: Do I have to calibrate new dyes on my Applied Biosystems 7500 or QuantStudio 5 Real-Time PCR System?
FAQ ID - 3732
表示
How long does a run take?
FAQ ID -2566
表示
Investigator Quantiplex: For which real-time cyclers has the kit been validated?
FAQ ID -2567
表示
What are the storage conditions?
FAQ ID - 3748
表示
Investigator Quantiplex: Which version of the Rotor Gene-Q software can be used to run the kit?
FAQ ID -2568
表示
How can I streamline the quantification workflow?
FAQ ID - 3738
表示
Investigator Quantiplex Pro: Can the kit be run on the Rotor-Gene Q?
FAQ ID - 3729
表示
Investigator Quantiplex Pro RGQ: On which real-time cyclers is the kit validated?
FAQ ID - 3741
表示
Can I optimize a dPCR assay on the QIAcuity using gradient temperature?
FAQ ID - 3783
表示
Are TaqMan® Gene Expression Assays from Applied Biosystems compatible with Rotor-Gene Probe Kits?
FAQ ID -2126
表示
Are probes other than TaqMan® probes, such as FRET probes, compatible with fast cycling with the Rotor-Gene Multiplex PCR Kit?
FAQ ID -2130
表示
Are TaqMan® Gene Expression Assays from Applied Biosystems compatible with the Rotor-Gene Multiplex PCR Kit?
FAQ ID -2131
表示
What is the difference between QIAGEN Protease and QIAGEN Proteinase K provided in various QIAamp Kits?
FAQ ID -761
表示
Can I use REPLI-g for SNP Genotyping?
FAQ ID -700
表示
Can other probe technologies besides TaqMan® be used with the Type-it Fast SNP Probe PCR Kit?
FAQ ID -2058
表示
What downstream applications have been tested with DNA purified using the PAXgene Blood DNA System?
FAQ ID - 3506
表示
Can the QuantiFast Pathogen PCR +IC Kit or the QuantiFast Pathogen RT-PCR +IC Kit be used with hybridization probes?
FAQ ID -2595
表示
Can I use the QuantiTect Multiplex PCR Kits on the Roche LightCycler systems with TaqMan® probes or QuantiTect Assays?
FAQ ID -717
表示
Can the QuantiFast Multiplex PCR Kits be used on Roche LightCycler systems with TaqMan® probes?
FAQ ID -1979
表示
Are TaqMan® Gene Expression Assays from Applied Biosystems compatible with QuantiFast Probe PCR Kits?
FAQ ID -1452
表示
How is "Touchdown PCR" used to increase PCR specificity?
FAQ ID -75
表示
What should the starting template DNA quality and quantity be for PCR?
FAQ ID -74
表示
What kind of PCR products can be cloned with the QIAGEN PCR Cloning Kit?
FAQ ID -165
表示
Why do I get smeared PCR products?
FAQ ID -87
表示
Does QIAGEN sell Q-Solution separately?
FAQ ID -204
表示
Do CoralLoad dyes supplied in various QIAGEN PCR Kits interfere with downstream applications?
FAQ ID -1745
表示
Is Q-Solution required for PCR with QIAGEN's PCR kits?
FAQ ID -380
表示
Have you tested the effect of inhibitors on PCR performance?
FAQ ID -818
表示
What is the composition of the QIAGEN 10x PCR Buffer in Taq- and HotStarTaq DNA Polymerase Kits?
FAQ ID -606
表示
Do you have to use a restriction enzyme to relieve ITR secondary structures and increase target accessibility?
FAQ ID - 3974
表示
What is the recommended HpaII concentration?
FAQ ID - 3976
表示
Can I use the lysate from the CGT Viral Vector Lysis kit and combine it with another PCR system?
FAQ ID - 3979
表示
Do you have any recommendations on how to process my AAV samples?
FAQ ID - 3860
表示
What can be done if lower and upper alignment markers used with the QIAxcel System or QIAxcel Advanced are not aligned correctly?
FAQ ID -1834
表示
How do I safely inactivate biohazardous flow-through material?
FAQ ID -12
表示
How should I store plant material for DNA isolation using the DNeasy Plant Kit?
FAQ ID -114
表示
How can I precipitate genomic DNA using isopropanol?
FAQ ID -2953
表示
How do I perform a DNA precipitation to concentrate my sample?
FAQ ID -305
表示
What can be used as an alternative to the A260 measurement for quantification of small amounts of RNA and DNA?
FAQ ID -728
表示
What is the composition of buffer AE?
FAQ ID -730
表示
Do I need to have EDTA in the buffer in which I am going to store my isolated genomic DNA?
FAQ ID -754
表示
Do you have a protocol for the isolation of DNA from tofu?
FAQ ID -932
表示
Does the Epitect Bisulfite Kit also work on DNA extracted from plants?
FAQ ID -1209
表示
What QIAGEN kit can I use to isolate DNA from food products to test for genetically modified organisms (GMOs)?
FAQ ID -371
表示
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