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What are the structures of the siRNA molecules used in RNAi studies?
FAQ ID -2760
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What are the critical factors in designing the siRNA molecules to be used for RNAi studies?
FAQ ID -2759
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Why is my EpiTect Methyl qPCR Assay "failed" as indicated in the QC page of the data analysis Excel file?
FAQ ID -2734
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Why is the qRT-PCR reproducibility so critical when detecting gene expression knock down in an RNAi experiment?
FAQ ID -2774
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Can miScript miRNA qPCR Assays be used for pre-miRNA detection?
FAQ ID -2724
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Can miScript miRNA qPCR Assays detect single nucleotide difference between miRNAs?
FAQ ID -2723
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Do I need an internal methylated DNA reference in the EpiTect Methyl qPCR Array?
FAQ ID -2736
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Do I need the sequence specific miRNA primers in the RT step of the miRNA qPCR Assays?
FAQ ID -2725
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Do you always run samples in triplicates?
FAQ ID -2703
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Can you use stained (H & E) sections with RT² PreAMP cDNA Synthesis Kit?
FAQ ID -2722
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Does this method with the EpiTect Methyl qPCR Array detect methylation at specific CpG dinucleotides?
FAQ ID -2737
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Does QIAGEN guarantee the performance of the SureSilencing shRNA Plasmids?
FAQ ID -2787
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Can I make stable cell lines with the Cignal Reporter Assays?
FAQ ID -2763
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How are the primers in the EpiTect Methyl qPCR Array designed?
FAQ ID -2735
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Is it acceptable to correct for transfection efficiency, when determining the level of gene expression knock down by an shRNA expression vector?
FAQ ID -2783
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Should I use monoclonal or polyclonal antibodies in EpiTect ChIP assays?
FAQ ID -2747
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What are the advantages of using the SureSilencing shRNA Plasmids over siRNA?
FAQ ID -2786
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The pathway reporter luciferase activity values are greater than the positive control, is there a problem?
FAQ ID -2766
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The EpiTect ChIP qPCR primers I used show very high Ct. Are there any solutions?
FAQ ID -2750
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The pathway reporter luciferase activity values are less than the negative control, is there a problem?
FAQ ID -2767
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How can I prevent the evaporation of reaction volume from the wells EpiTect Methyl qPCR Arrays?
FAQ ID -2742
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How can RNA interference be used as a life science research tool?
FAQ ID -2756
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How can I be sure that the restriction enzyme digestion is complete in the EpiTect Methyl qPCR system?
FAQ ID -2731
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How can I normalize my EpiTect ChIP results?
FAQ ID -2751
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What is the recommended amount of input template for each RT² qPCR Primer Assay?
FAQ ID -2716
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What is the RT² Profiler PCR Array?
FAQ ID -2718
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Can the EpiTect Methyl qPCR System technology reliably characterize heterogenous tissue samples?
FAQ ID -2732
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Can users insert custom transcriptional regulatory elements or promoters into the Cignal Reporter Assays?
FAQ ID -2765
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Can you custom design the Epitect qPCR primers for the CpG island outside of the defined promoter region?
FAQ ID -2744
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Can I manually set the threshold line?
FAQ ID -2702
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Can I use your EpiTect One-Day kit with transcription factors?
FAQ ID -2752
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Can I obtain the sequence of the RT² qPCR Primer Assay that I purchased?
FAQ ID -2709
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Are EpiTect Methyl qPCR Arrays or Assays applicable to FFPE samples?
FAQ ID -2733
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Are there any unique elements that need to be incorporated into an shRNA expression vector?
FAQ ID -2772
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Can I use the default PCR program to run EpiTect Methyl qPCR Arrays or Assays?
FAQ ID -2745
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Can I use total RNA for the miRNA PCR Arrays or Assays?
FAQ ID -2726
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Can I reliably detect intermediately methylated DNA with EpiTect Methyl qPCR Array technology?
FAQ ID -2738
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Can I use your EpiTect ChIP system in a RNA study?
FAQ ID -2748
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Can I transform the Cignal Reporter Assays?
FAQ ID -2762
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How many experiments can I do with the Cignal Lenti Reporter Assays?
FAQ ID -2769
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Can I use fluorescence microscopy to assess shRNA plasmid transfection efficiency in my model cell line of interest, when using a vector expressing a GFP reporter gene?
FAQ ID -2782
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How many housekeeping genes are included in each PCR Array?
FAQ ID -2704
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How reliable are the results from the miScript Primer Assays?
FAQ ID -2730
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What are EpiTect ChIP qPCR Assays?
FAQ ID -2720
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What are the advantages of EpiTect ChIP qPCR Assays and Arrays?
FAQ ID -2721
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How do I choose EpiTect ChIP-grade antibodies?
FAQ ID -2746
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How do you determine the efficiency using the PCR array?
FAQ ID -2701
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How does QIAGEN control the quality of the RT² qPCR Primer Assays?
FAQ ID -2711
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How do I choose between the DNA-based Cignal Reporter Assays and the Cignal Lenti Reporter Assays?
FAQ ID -2761
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Is the Microbial qPCR mastermix used in the Microbial DNA assay and in the Microbial DNA arrays free of genomic bacterial DNA?
FAQ ID - 3535
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The QIAsymphony RNA kit uses RLT plus as lysis buffer. Can samples lysed in RLT and then stored in the freezer be used on the QIAsymphony?
FAQ ID - 3533
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Can smaller volumes of blood be processed from the PAXgene Blood DNA Tube?
FAQ ID - 3500
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How should DNA purified using the PAXgene Blood DNA System be stored?
FAQ ID - 3502
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Is it possible to interrupt the PAXgene Blood DNA kit protocol?
FAQ ID - 3503
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Can I use the PAXgene Blood DNA Tube to collect blood from animals?
FAQ ID - 3504
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Can PAXgene Blood DNA Tubes be stored at higher than room temperature (18–25°C)?
FAQ ID - 3509
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What kind of starting material can be used with the REPLI-g Single Cell DNA Library Kit?
FAQ ID - 3536
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What is the maximum/minimum amount of DNA that can be used with REPLI-g Single Cell DNA Library Kit?
FAQ ID - 3537
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Does the REPLI-g Single Cell DNA Library Kit include adapters?
FAQ ID - 3538
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Does the REPLI-g Single Cell DNA Library Kit include a size selection step?
FAQ ID - 3539
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Is the REPLI-g Single Cell DNA Library Kit compatible with adapters and amplification primers from other suppliers?
FAQ ID - 3540
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Do I have to amplify the libraries generated with REPLI-g Single Cell DNA Library Kit to obtain full-length adapter sequences?
FAQ ID - 3541
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What is the enzyme used in the whole genome amplification step?
FAQ ID - 3542
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Which cell collection methods are compatible with REPLI-g Single Cell DNA Library Kit?
FAQ ID - 3543
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Should cells be washed before collection?
FAQ ID - 3544
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What is the sample input volume for the REPLI-g Single Cell DNA Library Kit?
FAQ ID - 3545
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Are there special requirements for flow sorting?
FAQ ID - 3546
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Does the REPLI-g Single Cell RNA Library Kit include a size selection step?
FAQ ID - 3551
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Does the REPLI-g Single Cell RNA Library Kit include adapters?
FAQ ID - 3550
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Is the REPLI-g Single Cell RNA Library Kit compatible with adapters and amplification primers from other suppliers?
FAQ ID - 3552
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