PrimePCR™ SYBR® Green Assay: REM1, 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 qHsaCIP0030313

List Price:    $174.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCID0016003
Assay Design:   Intron-spanning
Chromosome Location:   20:30064476-30065665question
Amplicon Length:   118
Splice Variants Targeted:   ENST00000201979

Gene Information

The protein encoded by this gene is a GTPase and member of the RAS-like GTP-binding protein family. The encoded protein is expressed in endothelial cells where it promotes reorganization of the actin cytoskeleton and morphological changes in the cells. [provided by RefSeq Jul 2008]

Gene Symbol:   REM1
Gene Name:   RAS (RAD and GEM)-like GTP-binding 1
Aliases:   GD:REM, GES, MGC48669, REM
RefSeq:   NC_000020.10 NT_011362.10
Ensembl:   ENSG00000088320
Entrez:   28954
Chromosome Mapping:   20q11.21

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 0.999700
y-intercept 35.070000
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.

Number Description Download
10039761 PrimePCR™ Assays Quick Guide, Ver B Click to download