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Can the miScript Single Cell qPCR Kit be used to quantify piRNA expression?
FAQ ID - 3567
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Can the miScript Single Cell qPCR Kit be used with plant cells?
FAQ ID - 3568
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Are any of the miScript Single Cell qPCR Kit components interchangeable with miScript II RT Kit, miScript Plant RT Kit, miScript PreAMP PCR Kit, or miScript Microfluidics PreAMP Kit components?
FAQ ID - 3569
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Should miScript PreAMP Primer Mixes be used in conjunction with the miScript Single Cell qPCR Kit?
FAQ ID - 3570
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Is the cDNA cleanup step in the miScript Single Cell qPCR Kit workflow absolutely required?
FAQ ID - 3571
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I have accidentally pipetted beads when removing the eluate after cDNA cleanup. What should I do?
FAQ ID - 3572
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Does the miScript Single Cell qPCR Kit contain controls?
FAQ ID - 3574
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When performing real-time PCR quality control associated with the miScript Single Cell qPCR Kit, is it necessary to perform control experiments for all individual samples/cells?
FAQ ID - 3576
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I do not see any miRNA expression for my miRNAs of interest after performing single cell miRNA expression analysis with the miScript Single Cell qPCR Kit and miScript miRNA PCR Arrays or miScript Primer Assays. What could be the cause?
FAQ ID - 3577
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What is the amplicon size of PCR products generated with the miScript Single Cell qPCR System?
FAQ ID - 3578
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What is the dissociation curve temperature of PCR products generated with the miScript Single Cell qPCR System?
FAQ ID - 3579
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When performing real-time PCR quality control associated with the miScript Single Cell qPCR Kit, is it necessary to perform control experiments for all individual samples/cells?
FAQ ID - 3575
View
How should data be analyzed when the miScript Single Cell qPCR Kit is used with miScript miRNA PCR Arrays or miScript Primer Assays?
FAQ ID - 3581
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Do you recommend normalizing single cell miRNA expression data to a “housekeeping” gene or miRNA?
FAQ ID - 3580
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What single cell isolation methods are recommended for use with the miScript Single Cell qPCR Kit?
FAQ ID - 3582
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How would I provide information on the QuantiTect Primer assays in publications when the sequence is confidential?
FAQ ID - 3593
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In which tubes is clot detection possible on QIAsymphony?
FAQ ID - 3589
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Which barcodes on sample tubes are accepted by the QIAsymphony SP?
FAQ ID - 3598
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Is it possible to measure the proteolytic activity of proteins on the surface of exosomes that were isolated with ExoEasy?
FAQ ID - 3599
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How can I create a report/logfile on my QIAsymphony SP system?
FAQ ID - 3594
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Can I change the language on my QIAsymphony SP system?
FAQ ID - 3595
View
Can the Rotor-Gene Q be connected to LIMS?
FAQ ID - 3596
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Can the REPLI-g Mitochondrial DNA Kit be used for species other than humans?
FAQ ID - 3584
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Can I use blood, cells or bacteria with the QIAamp Fast DNA Tissue Kit?
FAQ ID - 3587
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What is MOI?
FAQ ID -2768
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What file format and layout do I need to upload my data into the PCR Array Data Analysis software?
FAQ ID -2700
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What does the RT² qPCR Primer Assay product information mean when it says that it recognizes another transcript of the same gene?
FAQ ID -2712
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What do I need in order to set up an RNAi experiment?
FAQ ID -2757
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What does a typical EpiTect Methyl qPCR Assay or Array include?
FAQ ID -2740
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Why did the real-time PCR yield Ct values < 12?
FAQ ID -2727
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Why can't I find the DNA methylation qPCR Assay for my gene of interest?
FAQ ID -2743
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Why do I need to identify my real-time instrument model when placing my order for RT² qPCR Primer Assays?
FAQ ID -2713
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What would happen if I used home-made PCR master mixes or master mixes from other manufacturers with the RT² products?
FAQ ID -2715
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Why are the RT² qPCR Primer Assays not designed to cross exon-intron junctions or boundaries?
FAQ ID -2710
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Which qPCR instrument should I use with your RT² qPCR Primer Assays?
FAQ ID -2714
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Why should I use RT² SYBR Green Mastermix with RT² qPCR Primer Assays?
FAQ ID -2706
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Will pipetting error affect the EpiTect Methyl qPCR Array results?
FAQ ID -2741
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Will pipetting error affect the miRNA qPCR Assay results?
FAQ ID -2728
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Why had my RT² SYBR Green Mastermix been working well in the past, but now does not seem to be?
FAQ ID -2717
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What RT² qPCR Primer Assays are available?
FAQ ID -2708
View
What MOI should I use for my cells?
FAQ ID -2770
View
What is the most reliable transfection reagent for delivering shRNA plasmids and siRNA to cells in culture?
FAQ ID -2777
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What transfection reagents are compatible with the Cignal Reporter Assays?
FAQ ID -2764
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What is included in the SureSilencing shRNA Plasmids shipment?
FAQ ID -2785
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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
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What are the key parameters contributing to unwanted off-target effects in an RNAi experiment?
FAQ ID -2775
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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 QIAGEN guarantee the performance of the SureSilencing shRNA Plasmids?
FAQ ID -2787
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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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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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On which instrumentation will the RT² Profiler PCR Array work?
FAQ ID -2719
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What are the advantages of using the SureSilencing shRNA Plasmids over siRNA?
FAQ ID -2786
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Should I use monoclonal or polyclonal antibodies in EpiTect ChIP assays?
FAQ ID -2747
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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 greater than the positive control, is there a problem?
FAQ ID -2766
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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 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
Can I manually set the threshold line?
FAQ ID -2702
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
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Can I use your EpiTect ChIP system in a RNA study?
FAQ ID -2748
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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 transform the Cignal Reporter Assays?
FAQ ID -2762
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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 experiments can I do with the Cignal Lenti Reporter Assays?
FAQ ID -2769
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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 the advantages of EpiTect ChIP qPCR Assays and Arrays?
FAQ ID -2721
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What are EpiTect ChIP qPCR Assays?
FAQ ID -2720
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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
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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
View
Which Microbial qPCR Mastermix should I use?
FAQ ID — 3395
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What are the storage conditions for the Microbial DNA qPCR products?
FAQ ID — 3394
View
3326 - Which QIAcube standard protocol might be suitable to extract RNA from saliva or from a buccal cell pellet?
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3327 - How often should the o-ring for the pipettor tip-adapter be changed on the QIAcube?
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3330 - Is there any contamination from E. coli genomic DNA in the polymerase provided with the Repli-G Single Cell Kit?
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