qPCR Human Reference cDNA, Oligo(dT)-primed

qPCR Human Reference cDNA, Oligo(dT)-primed

Brand: Takara Bio.
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qPCR Human Reference cDNA, Oligo(dT)-primed
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qPCR Human Reference cDNA, Oligo(dT)-primed
SKU: 636692
25 Rxns
qPCR Human Reference cDNA, Oligo(dT)-primed
SKU: 636693
100 Rxns
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qPCR Human Reference cDNA, Oligo(dT)-primed
qPCR Human Reference cDNA, Oligo(dT)-primed

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Reference cDNA for real-time qPCR

cDNAs prepared from a mixture of total RNAs collected from adult normal human tissues. This cDNA mixture has been chosen to represent a broad range of expressed genes.

qPCR Human Reference cDNA serves as a standard for accurate and reproducible comparison of gene expression data using qPCR (quantitative PCR) as well as a positive control template for validation of gene primer design. Enough cDNA is supplied for either 25 or 100 reactions requiring 2 μl of sample per reaction; the number of reactions is based on a 50 μl reaction volume.

The sample was oligo(dT) primed.

Overview

  • Broad gene coverage
  • Virtually free of genomic DNA
  • Made from human tissues, not cultured cell lines
  • A high-performance standard for quantitative PCR

Applications

  • Real-time PCR/qPCR
  • Gene expression analysis
  • One-step RT-PCR
  • Northern analysis
  • Microarray analysis

High-, medium- and low-abundance gene targets are easily detected in qPCR Human Reference cDNA

High-, medium- and low-abundance gene targets are easily detected in qPCR Human Reference cDNA

High-, medium- and low-abundance gene targets are easily detected in qPCR Human Reference cDNA. Oligo dT-primed (Panels A–C) and random oligo-primed (Panels D–F) qPCR Human Reference cDNA samples were each serially diluted fivefold such that the final quantities of cDNA template in the qPCR reactions were 20 ng, 4 ng, 800 pg, 160 pg, 32 pg,and 6.4 pg. Data were obtained on a Stratagene Mx3000P real-time PCR instrument. The primer sets for all three genes demonstrate the ability to detect a wide range of signals from the serially diluted samples. PPIA = peptidylprolyl isomerase A (cyclophilin A; high-abundance); HPRT = hypoxanthine phosphoribosyltransferase I (medium-abundance); PBGD = porphobilinogen deaminase (low-abundance). Slope and R2 values refer to the line determinedby plotting Ct values versus template quantity

Reference

Suzuki, T., Higgins, P. J. & Crawford, D. R. Control selection for RNA quantitation. Biotechniques 29, 332–7 (2000).   

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Reference cDNA for real-time qPCR

cDNAs prepared from a mixture of total RNAs collected from adult normal human tissues. This cDNA mixture has been chosen to represent a broad range of expressed genes.

qPCR Human Reference cDNA serves as a standard for accurate and reproducible comparison of gene expression data using qPCR (quantitative PCR) as well as a positive control template for validation of gene primer design. Enough cDNA is supplied for either 25 or 100 reactions requiring 2 μl of sample per reaction; the number of reactions is based on a 50 μl reaction volume.

The sample was oligo(dT) primed.

Overview

  • Broad gene coverage
  • Virtually free of genomic DNA
  • Made from human tissues, not cultured cell lines
  • A high-performance standard for quantitative PCR

Applications

  • Real-time PCR/qPCR
  • Gene expression analysis
  • One-step RT-PCR
  • Northern analysis
  • Microarray analysis

High-, medium- and low-abundance gene targets are easily detected in qPCR Human Reference cDNA

High-, medium- and low-abundance gene targets are easily detected in qPCR Human Reference cDNA

High-, medium- and low-abundance gene targets are easily detected in qPCR Human Reference cDNA. Oligo dT-primed (Panels A–C) and random oligo-primed (Panels D–F) qPCR Human Reference cDNA samples were each serially diluted fivefold such that the final quantities of cDNA template in the qPCR reactions were 20 ng, 4 ng, 800 pg, 160 pg, 32 pg,and 6.4 pg. Data were obtained on a Stratagene Mx3000P real-time PCR instrument. The primer sets for all three genes demonstrate the ability to detect a wide range of signals from the serially diluted samples. PPIA = peptidylprolyl isomerase A (cyclophilin A; high-abundance); HPRT = hypoxanthine phosphoribosyltransferase I (medium-abundance); PBGD = porphobilinogen deaminase (low-abundance). Slope and R2 values refer to the line determinedby plotting Ct values versus template quantity

Reference

Suzuki, T., Higgins, P. J. & Crawford, D. R. Control selection for RNA quantitation. Biotechniques 29, 332–7 (2000).   

Write Your Own Review
You're reviewing:qPCR Human Reference cDNA, Oligo(dT)-primed
Your Rating