PrimePCR™ Probe Assay: RHAG, 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:   qHsaCEP0050680
Assay Design:   exonic
Chromosome Location:   6:49586903-49587041question
Amplicon Length:   109
Splice Variants Targeted:   ENST00000371175 ENST00000229810

Gene Information

The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN) or Rh-deficiency syndrome.[provided by RefSeq Mar 2009]

Gene Symbol:   RHAG
Gene Name:   Rh-associated glycoprotein
Aliases:   CD241, RH2, RH50A, Rh50, Rh50GP, SLC42A1
RefSeq:   NC_000006.11 NG_011704.1 NT_007592.15
Ensembl:   ENSG00000112077
Entrez:   6005
Chromosome Mapping:   6p21.1-p11

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 0.999100
y-intercept 35.680000
Efficiency 101

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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