Product FAQ - QIAGEN



Product FAQ Bookmark Share more.. You are not authorized to download the resource Sort options Sort alphabetically Sort by relevance Sorted by relevance What are the structures of the siRNA molecules used in RNAi studies? FAQ ID -2760 View What are the critical factors in designing the siRNA molecules to be used for RNAi studies? FAQ ID -2759 View Why is my EpiTect Methyl qPCR Assay "failed" as indicated in the QC page of the data analysis Excel file? FAQ ID -2734 View Why is the qRT-PCR reproducibility so critical when detecting gene expression knock down in an RNAi experiment? FAQ ID -2774 View Can miScript miRNA qPCR Assays be used for pre-miRNA detection? FAQ ID -2724 View Can miScript miRNA qPCR Assays detect single nucleotide difference between miRNAs? FAQ ID -2723 View Do I need an internal methylated DNA reference in the EpiTect Methyl qPCR Array? FAQ ID -2736 View Do I need the sequence specific miRNA primers in the RT step of the miRNA qPCR Assays? FAQ ID -2725 View Do you always run samples in triplicates? FAQ ID -2703 View Can you use stained (H & E) sections with RT² PreAMP cDNA Synthesis Kit? FAQ ID -2722 View Does this method with the EpiTect Methyl qPCR Array detect methylation at specific CpG dinucleotides? FAQ ID -2737 View Does QIAGEN guarantee the performance of the SureSilencing shRNA Plasmids? FAQ ID -2787 View Can I make stable cell lines with the Cignal Reporter Assays? FAQ ID -2763 View How are the primers in the EpiTect Methyl qPCR Array designed? FAQ ID -2735 View 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 View Should I use monoclonal or polyclonal antibodies in EpiTect ChIP assays? FAQ ID -2747 View What are the advantages of using the SureSilencing shRNA Plasmids over siRNA? FAQ ID -2786 View The pathway reporter luciferase activity values are greater than the positive control, is there a problem? FAQ ID -2766 View The EpiTect ChIP qPCR primers I used show very high Ct. Are there any solutions? FAQ ID -2750 View The pathway reporter luciferase activity values are less than the negative control, is there a problem? FAQ ID -2767 View How can I prevent the evaporation of reaction volume from the wells EpiTect Methyl qPCR Arrays? FAQ ID -2742 View How can RNA interference be used as a life science research tool? FAQ ID -2756 View How can I be sure that the restriction enzyme digestion is complete in the EpiTect Methyl qPCR system? FAQ ID -2731 View How can I normalize my EpiTect ChIP results? FAQ ID -2751 View What is the recommended amount of input template for each RT² qPCR Primer Assay? FAQ ID -2716 View What is the RT² Profiler PCR Array? FAQ ID -2718 View Can the EpiTect Methyl qPCR System technology reliably characterize heterogenous tissue samples? FAQ ID -2732 View Can users insert custom transcriptional regulatory elements or promoters into the Cignal Reporter Assays? FAQ ID -2765 View Can you custom design the Epitect qPCR primers for the CpG island outside of the defined promoter region? FAQ ID -2744 View Can I manually set the threshold line? FAQ ID -2702 View Can I use your EpiTect One-Day kit with transcription factors? FAQ ID -2752 View Can I obtain the sequence of the RT² qPCR Primer Assay that I purchased? FAQ ID -2709 View Are EpiTect Methyl qPCR Arrays or Assays applicable to FFPE samples? FAQ ID -2733 View Are there any unique elements that need to be incorporated into an shRNA expression vector? FAQ ID -2772 View Can I use the default PCR program to run EpiTect Methyl qPCR Arrays or Assays? FAQ ID -2745 View Can I use total RNA for the miRNA PCR Arrays or Assays? FAQ ID -2726 View Can I reliably detect intermediately methylated DNA with EpiTect Methyl qPCR Array technology? FAQ ID -2738 View Can I use your EpiTect ChIP system in a RNA study? FAQ ID -2748 View Can I transform the Cignal Reporter Assays? FAQ ID -2762 View How many experiments can I do with the Cignal Lenti Reporter Assays? FAQ ID -2769 View 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 View How many housekeeping genes are included in each PCR Array? FAQ ID -2704 View How reliable are the results from the miScript Primer Assays? FAQ ID -2730 View What are EpiTect ChIP qPCR Assays? FAQ ID -2720 View What are the advantages of EpiTect ChIP qPCR Assays and Arrays? FAQ ID -2721 View How do I choose EpiTect ChIP-grade antibodies? FAQ ID -2746 View How do you determine the efficiency using the PCR array? FAQ ID -2701 View How does QIAGEN control the quality of the RT² qPCR Primer Assays? FAQ ID -2711 View How do I choose between the DNA-based Cignal Reporter Assays and the Cignal Lenti Reporter Assays? FAQ ID -2761 View 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 View 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 View Can smaller volumes of blood be processed from the PAXgene Blood DNA Tube? FAQ ID - 3500 View How should DNA purified using the PAXgene Blood DNA System be stored? FAQ ID - 3502 View Is it possible to interrupt the PAXgene Blood DNA kit protocol? FAQ ID - 3503 View Can I use the PAXgene Blood DNA Tube to collect blood from animals? FAQ ID - 3504 View Can PAXgene Blood DNA Tubes be stored at higher than room temperature (18–25°C)? FAQ ID - 3509 View What kind of starting material can be used with the REPLI-g Single Cell DNA Library Kit? FAQ ID - 3536 View What is the maximum/minimum amount of DNA that can be used with REPLI-g Single Cell DNA Library Kit? FAQ ID - 3537 View Does the REPLI-g Single Cell DNA Library Kit include adapters? FAQ ID - 3538 View Does the REPLI-g Single Cell DNA Library Kit include a size selection step? FAQ ID - 3539 View Is the REPLI-g Single Cell DNA Library Kit compatible with adapters and amplification primers from other suppliers? FAQ ID - 3540 View 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 View What is the enzyme used in the whole genome amplification step? FAQ ID - 3542 View Which cell collection methods are compatible with REPLI-g Single Cell DNA Library Kit? FAQ ID - 3543 View Should cells be washed before collection? FAQ ID - 3544 View What is the sample input volume for the REPLI-g Single Cell DNA Library Kit? FAQ ID - 3545 View Are there special requirements for flow sorting? FAQ ID - 3546 View Does the REPLI-g Single Cell RNA Library Kit include a size selection step? FAQ ID - 3551 View Does the REPLI-g Single Cell RNA Library Kit include adapters? FAQ ID - 3550 View Is the REPLI-g Single Cell RNA Library Kit compatible with adapters and amplification primers from other suppliers? FAQ ID - 3552 View Show more results Back to top Contact QIAGEN Global contacts Technical Service Customer Care