PrimePCR™ SYBR® Green Assay: RANGAP1, 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 qHsaCIP0027137

List Price:    $142.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCID0009302
Assay Design:   Intron-spanning
Chromosome Location:   22:41645765-41647077question
Amplicon Length:   94
Splice Variants Targeted:   ENST00000405486 ENST00000356244 ENST00000405383 ENST00000455915 ENST00000407260

Gene Information

RanGAP1 is a homodimeric 65-kD polypeptide that specifically induces the GTPase activity of RAN but not of RAS by over 1000-fold. RanGAP1 is the immediate antagonist of RCC1 a regulator molecule that keeps RAN in the active GTP-bound state. The RANGAP1 gene encodes a 587-amino acid polypeptide. The sequence is unrelated to that of GTPase activators for other RAS-related proteins but is 88% identical to Fug1 the murine homolog of yeast Rna1p. RanGAP1 and RCC1 control RAN-dependent transport between the nucleus and cytoplasm. RanGAP1 is a key regulator of the RAN GTP/GDP cycle. [provided by RefSeq Jul 2008]

Gene Symbol:   RANGAP1
Gene Name:   Ran GTPase activating protein 1
Aliases:   Fug1, KIAA1835, MGC20266, SD
RefSeq:   NC_000022.10 NT_011520.12
Ensembl:   ENSG00000100401
Entrez:   5905
UniGene:   Hs.183800
Chromosome Mapping:   22q13

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 0.999300
y-intercept 34.610000
Efficiency 102

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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