PrimePCR™ SYBR® Green Assay: PHGDH, 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

List Price:    $142.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCID0011923
Assay Design:   Intron-spanning
Chromosome Location:   1:120263882-120269483question
Amplicon Length:   108
Splice Variants Targeted:   ENST00000369409 ENST00000369407 ENST00000537497 ENST00000535091

Gene Information

This gene encodes the enzyme which is involved in the early steps of L-serine synthesis in animal cells. L-serine is required for D-serine and other amino acid synthesis. The enzyme requires NAD/NADH as a cofactor and forms homotetramers for activity. Mutations in this gene have been found in a family with congenital microcephaly psychomotor retardation and other symptoms. Multiple alternatively spliced transcript variants have been found however the full-length nature of most are not known. [provided by RefSeq Aug 2011]

Gene Symbol:   PHGDH
Gene Name:   phosphoglycerate dehydrogenase
Aliases:   3-PGDH, 3PGDH, MGC3017, PDG, PGAD, PGD, PGDH, SERA
RefSeq:   NC_000001.10 NG_009188.1 NT_032977.9
Ensembl:   ENSG00000092621
Entrez:   26227
UniGene:   Hs.487296
Chromosome Mapping:   1p12

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 0.998200
y-intercept 35.700000
Efficiency 93

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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