Frequently Asked Questions - FAQ



FAQ Bookmark シェア more.. You are not authorized to download the resource Sort options アルファベット順関連順 Does this method with the EpiTect Methyl qPCR Array detect methylation at specific CpG dinucleotides? FAQ ID -2737 表示 Does QIAGEN guarantee the performance of the SureSilencing shRNA Plasmids? FAQ ID -2787 表示 Can I make stable cell lines with the Cignal Reporter Assays? FAQ ID -2763 表示 How are the primers in the EpiTect Methyl qPCR Array designed? FAQ ID -2735 表示 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 表示 Should I use monoclonal or polyclonal antibodies in EpiTect ChIP assays? FAQ ID -2747 表示 What are the advantages of using the SureSilencing shRNA Plasmids over siRNA? FAQ ID -2786 表示 The pathway reporter luciferase activity values are greater than the positive control, is there a problem? FAQ ID -2766 表示 The EpiTect ChIP qPCR primers I used show very high Ct. Are there any solutions? FAQ ID -2750 表示 The pathway reporter luciferase activity values are less than the negative control, is there a problem? FAQ ID -2767 表示 How can I prevent the evaporation of reaction volume from the wells EpiTect Methyl qPCR Arrays? FAQ ID -2742 表示 How can RNA interference be used as a life science research tool? FAQ ID -2756 表示 How can I be sure that the restriction enzyme digestion is complete in the EpiTect Methyl qPCR system? FAQ ID -2731 表示 How can I normalize my EpiTect ChIP results? FAQ ID -2751 表示 What is the recommended amount of input template for each RT² qPCR Primer Assay? FAQ ID -2716 表示 What is the RT² Profiler PCR Array? FAQ ID -2718 表示 Can the EpiTect Methyl qPCR System technology reliably characterize heterogenous tissue samples? FAQ ID -2732 表示 Can users insert custom transcriptional regulatory elements or promoters into the Cignal Reporter Assays? FAQ ID -2765 表示 Can you custom design the Epitect qPCR primers for the CpG island outside of the defined promoter region? FAQ ID -2744 表示 Can I manually set the threshold line? FAQ ID -2702 表示 Can I use your EpiTect One-Day kit with transcription factors? FAQ ID -2752 表示 Can I obtain the sequence of the RT² qPCR Primer Assay that I purchased? FAQ ID -2709 表示 Are EpiTect Methyl qPCR Arrays or Assays applicable to FFPE samples? FAQ ID -2733 表示 Are there any unique elements that need to be incorporated into an shRNA expression vector? FAQ ID -2772 表示 Can I use the default PCR program to run EpiTect Methyl qPCR Arrays or Assays? FAQ ID -2745 表示 Can I use total RNA for the miRNA PCR Arrays or Assays? FAQ ID -2726 表示 Can I reliably detect intermediately methylated DNA with EpiTect Methyl qPCR Array technology? FAQ ID -2738 表示 Can I use your EpiTect ChIP system in a RNA study? FAQ ID -2748 表示 Can I transform the Cignal Reporter Assays? FAQ ID -2762 表示 How many experiments can I do with the Cignal Lenti Reporter Assays? FAQ ID -2769 表示 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 表示 How many housekeeping genes are included in each PCR Array? FAQ ID -2704 表示 How reliable are the results from the miScript Primer Assays? FAQ ID -2730 表示 What are EpiTect ChIP qPCR Assays? FAQ ID -2720 表示 What are the advantages of EpiTect ChIP qPCR Assays and Arrays? FAQ ID -2721 表示 How do I choose EpiTect ChIP-grade antibodies? FAQ ID -2746 表示 How do you determine the efficiency using the PCR array? FAQ ID -2701 表示 How does QIAGEN control the quality of the RT² qPCR Primer Assays? FAQ ID -2711 表示 How do I choose between the DNA-based Cignal Reporter Assays and the Cignal Lenti Reporter Assays? FAQ ID -2761 表示 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 表示 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 表示 Can smaller volumes of blood be processed from the PAXgene Blood DNA Tube? FAQ ID - 3500 表示 How should DNA purified using the PAXgene Blood DNA System be stored? FAQ ID - 3502 表示 Is it possible to interrupt the PAXgene Blood DNA kit protocol? FAQ ID - 3503 表示 Can I use the PAXgene Blood DNA Tube to collect blood from animals? FAQ ID - 3504 表示 Can PAXgene Blood DNA Tubes be stored at higher than room temperature (18–25°C)? FAQ ID - 3509 表示 What kind of starting material can be used with the REPLI-g Single Cell DNA Library Kit? FAQ ID - 3536 表示 What is the maximum/minimum amount of DNA that can be used with REPLI-g Single Cell DNA Library Kit? FAQ ID - 3537 表示 Does the REPLI-g Single Cell DNA Library Kit include adapters? FAQ ID - 3538 表示 Does the REPLI-g Single Cell DNA Library Kit include a size selection step? FAQ ID - 3539 表示 Is the REPLI-g Single Cell DNA Library Kit compatible with adapters and amplification primers from other suppliers? FAQ ID - 3540 表示 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 表示 What is the enzyme used in the whole genome amplification step? FAQ ID - 3542 表示 Which cell collection methods are compatible with REPLI-g Single Cell DNA Library Kit? FAQ ID - 3543 表示 Should cells be washed before collection? FAQ ID - 3544 表示 What is the sample input volume for the REPLI-g Single Cell DNA Library Kit? FAQ ID - 3545 表示 Are there special requirements for flow sorting? FAQ ID - 3546 表示 Does the REPLI-g Single Cell RNA Library Kit include a size selection step? FAQ ID - 3551 表示 Does the REPLI-g Single Cell RNA Library Kit include adapters? FAQ ID - 3550 表示 Is the REPLI-g Single Cell RNA Library Kit compatible with adapters and amplification primers from other suppliers? FAQ ID - 3552 表示 Do I have to amplify the libraries generated with REPLI-g Single Cell RNA Library Kit to obtain full-length adapter sequences? FAQ ID - 3553 表示 What is the enzyme used in the whole transcriptome amplification step? FAQ ID - 3554 表示 Which cell collection methods are compatible with REPLI-g Single Cell RNA Library Kit? FAQ ID - 3555 表示 Should cells be washed before collection? FAQ ID - 3556 表示 What is the sample input volume for REPLI-g Single Cell RNA Library Kit? FAQ ID - 3557 表示 Are there special requirements for flow sorting? FAQ ID - 3558 表示 What kind of starting material can be used with the REPLI-g Single Cell RNA Library Kit? FAQ ID - 3548 表示 What is the maximum/minimum amount of DNA that can be used with REPLI-g Single Cell RNA Library Kit? FAQ ID - 3549 表示 What is the expected purity of DNA extracted from blood samples collected in PAXgene Blood DNA Tubes IVD? FAQ ID - 3511 表示 Is the quality and size of DNA extracted with the QIAamp DNA Mini and QIAamp Blood Mini kit good enough to generate DNA-libraries for next generation sequencing (NGS)? FAQ ID - 3518 表示 How much protein does one vial of Protease in the QIAamp spin kits contain? What is the concentration of the resuspended Protease? FAQ ID - 3520 表示 What is the RT-PCR performance of RNA purified from PAXgene Tissue fixed, paraffin-embedded (PFPE) tissue compared to RNA from snap frozen or formalin-fixed, paraffin-embedded (FFPE) tissue? FAQ ID - 3514 表示 Where can I find additional information for PreAnalytiX PAXgene products? FAQ ID - 3515 表示 How can samples be shipped and stored prior to extraction on the Autopure LS? FAQ ID - 3522 表示 How does the liquid level detection work and what is the minimal detectable volume for the conductive tips of the BioRobot Universal? FAQ ID - 3524 表示 How can samples be shipped and stored prior to extraction on the Autopure LS? FAQ ID - 3528 表示 What is the pipetting throughput of the BioRobot Universal? FAQ ID - 3527 表示 How do I obtain the concentration of my gDNA from the data analysis using the GeneRead DNA QuantiMIZE? FAQ ID - 3530 表示 What is the pipetting throughput of the BioRobot Universal? FAQ ID - 3525 表示 What specification do you have for the high-speed shaker system of the BioRobot Universal? FAQ ID - 3526 表示次ページ Back to top Contact QIAGEN Global contacts Technical Service Customer Care