PrimePCR™ Probe Assay: SRA1, Human

RT

Real-time PCR probe assay designed for gene expression analysis. Probe assays consist of unlabeled PCR primers and a dual labeled fluorescent probe.

List Price:    $255.00
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Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCEP0040520
Assay Design:   exonic
Chromosome Location:   5:139929980-139930103question
Amplicon Length:   94
Splice Variants Targeted:   ENST00000336283

Gene Information

Both long non-coding and protein-coding RNAs are transcribed from this gene and they represent alternatively spliced transcript variants. This gene was initially defined as a non-coding RNA which is a coactivator for several nuclear receptors (NRs) and is associated with breast cancer. It has now been found that this gene is involved in the regulation of many NR and non-NR activities including metabolism adipogenesis and chromatin organization. The long non-coding RNA transcripts interact with a variety of proteins including the protein encoded by this gene. The encoded protein acts as a transcriptional repressor by binding to the non-coding RNA. [provided by RefSeq Mar 2012]

Gene Symbol:   SRA1
Gene Name:   steroid receptor RNA activator 1
Aliases:   MGC87674, SRA, SRAP, STRAA1, pp7684
RefSeq:   NC_000005.9 NT_029289.11
Ensembl:   ENSG00000213523
Entrez:   10011
Chromosome Mapping:   5q31.3

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™ SYBR® Green Supermix
Experimental Sample qPCR Human Reference Total RNA

Summary Data:

R2 0.999100
y-intercept 35.440000
Efficiency 99

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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