PrimePCR™ SYBR® Green Assay: RDH8, 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 qHsaCEP0049715

List Price:    $142.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCED0042453
Assay Design:   exonic
Chromosome Location:   19:10132420-10132563question
Amplicon Length:   114
Splice Variants Targeted:   ENST00000591589 ENST00000587782 ENST00000171214

Gene Information

All-trans-retinol dehydrogenase (RDH8) is a visual cycle enzyme that reduces all-trans-retinal to all-trans-retinol in the presence of NADPH (Rattner et al. 2000 [PubMed 10753906]). It is a member of the short chain dehydrogenase/reductase family and is located in the outer segments of photoreceptors; hence it is also known as photoreceptor retinol dehydrogenase. It is important in the visual cycle by beginning the rhodopsin regeneration pathway by reducing all-trans-retinal the product of bleached and hydrolysed rhodopsin (Rando 2001 [PubMed 11710234]). This is a rate-limiting step in the visual cycle (Saari et al. 1998 [PubMed 9667000]).[supplied by OMIM Mar 2008]

Gene Symbol:   RDH8
Gene Name:   retinol dehydrogenase 8 (all-trans)
Aliases:   PRRDH, SDR28C2
RefSeq:   NC_000019.9 NT_011295.11
Ensembl:   ENSG00000080511
Entrez:   50700
UniGene:   Hs.675522
Chromosome Mapping:   19p13.2

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 0.999600
y-intercept 37.060000
Efficiency 94

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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