PrimePCR™ SYBR® Green Assay: GFM1, 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:   Same primer pair as used in probe assay qHsaCIP0028401

List Price:    $142.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCID0012338
Assay Design:   Intron-spanning
Chromosome Location:   3:158378663-158380464question
Amplicon Length:   120
Splice Variants Targeted:   ENST00000486715 ENST00000478576 ENST00000264263

Gene Information

Eukaryotes contain two protein translational systems one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors. Its role in the regulation of normal mitochondrial function and in different disease states attributed to mitochondrial dysfunction is not known. [provided by RefSeq Jul 2008]

Gene Symbol:   GFM1
Gene Name:   G elongation factor, mitochondrial 1
Aliases:   COXPD1, EFG, EFG1, EFGM, EGF1, FLJ12662, FLJ13632, FLJ20773, GFM, hEFG1
RefSeq:   NC_000003.11 NG_008441.1 NT_005612.16
Ensembl:   ENSG00000168827
Entrez:   85476
UniGene:   Hs.518355
Chromosome Mapping:   3q25

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 0.999000
y-intercept 35.220000
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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