PrimePCR™ SYBR® Green Assay: TRIM28, Human

PrimePCR Primer Assays for Real-Time PCR oligo primer pair tube for SYBR Green gene expression

Real-time PCR primer assay designed for SYBR® Green gene expression analysis.

Info:   Recommended - best coverage; Same primer pair as used in probe assay qHsaCEP0051597

List Price:    $142.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCED0044335
Assay Design:   exonic
Chromosome Location:   19:59056904-59058751question
Amplicon Length:   113
Splice Variants Targeted:   ENST00000593582 ENST00000594806 ENST00000253024 ENST00000597968

Gene Information

The protein encoded by this gene mediates transcriptional control by interaction with the Kruppel-associated box repression domain found in many transcription factors. The protein localizes to the nucleus and is thought to associate with specific chromatin regions. The protein is a member of the tripartite motif family. This tripartite motif includes three zinc-binding domains a RING a B-box type 1 and a B-box type 2 and a coiled-coil region. [provided by RefSeq Jul 2008]

Gene Symbol:   TRIM28
Gene Name:   tripartite motif containing 28
Aliases:   FLJ29029, KAP1, RNF96, TF1B, TIF1B
RefSeq:   NC_000019.9 NT_011109.16
Ensembl:   ENSG00000130726
Entrez:   10155
UniGene:   Hs.467408
Chromosome Mapping:   19q13.4

The below validation information is for the Primer Pair only   Download Validation Data (.pdf)


Products used to generate validation data:

Real-Time PCR Instrument CFX384 Real-Time PCR Detection System
Reverse Transcription Reagent iScript™ Advanced cDNA Synthesis Kit for RT-qPCR
Real-Time PCR Supermix SsoAdvanced™ Universal SYBR® Green Supermix
Experimental Sample qPCR Human Reference Total RNA

Summary Data:

R2 0.999300
y-intercept 36.220000
Efficiency 95

Amplification Plot
Amplification of cDNA generated from universal RNA.

Amplification of cDNA generated from universal RNA.

Melt Peak
Melt curve analysis of above amplification.

Melt curve analysis of above amplification.

Standard Curve
Standard curve generated using 20 million copies of template diluted 10 fold to 20 copies.

Standard curve generated using 20 million copies of template diluted 10 fold to 20 copies.

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