PrimePCR™ SYBR® Green Assay: ST8SIA1, 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 qHsaCEP0050663

List Price:    $138.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCED0043401
Assay Design:   exonic
Chromosome Location:   12:22440224-22487064question
Amplicon Length:   108
Splice Variants Targeted:   ENST00000289382 ENST00000396037 ENST00000541868 ENST00000404299 ENST00000381424 ENST00000539510 ENST00000515877 ENST00000503738 ENST00000407583 ENST00000458167 ENST00000424214

Gene Information

Gangliosides are membrane-bound glycosphingolipids containing sialic acid. Ganglioside GD3 is known to be important for cell adhesion and growth of cultured malignant cells. The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to GM3 to produce gangliosides GD3 and GT3. The encoded protein may be found in the Golgi apparatus and is a member of glycosyltransferase family 29. [provided by RefSeq Jul 2008]

Gene Symbol:   ST8SIA1
Gene Name:   ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1
Aliases:   GD3S, SIAT8, SIAT8A, ST8SiaI
RefSeq:   NC_000012.11 NT_009714.17
Ensembl:   ENSG00000111728
Entrez:   6489
UniGene:   Hs.408614
Chromosome Mapping:   12p12.1-p11.2

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 0.999100
y-intercept 35.550000
Efficiency 101

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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