PrimePCR™ SYBR® Green Assay: TIAM2, 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 qHsaCEP0052589

List Price:    $146.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCED0045328
Assay Design:   exonic
Chromosome Location:   6:155566761-155569146question
Amplicon Length:   88
Splice Variants Targeted:   ENST00000461783 ENST00000528535 ENST00000360366 ENST00000529824 ENST00000456877 ENST00000528391 ENST00000275246 ENST00000462408 ENST00000456144 ENST00000318981 ENST00000367174

Gene Information

This gene encodes a guanine nucleotide exchange factor. A highly similar mouse protein specifically activates ras-related C3 botulinum substrate 1 converting this Rho-like guanosine triphosphatase (GTPase) from a guanosine diphosphate-bound inactive state to a guanosine triphosphate-bound active state. The encoded protein may play a role in neural cell development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq Jul 2008]

Gene Symbol:   TIAM2
Gene Name:   T-cell lymphoma invasion and metastasis 2
Aliases:   FLJ41865, STEF, TIAM-2
RefSeq:   NC_000006.11 NG_027528.1 NT_025741.15
Ensembl:   ENSG00000146426
Entrez:   26230
UniGene:   Hs.586279
Chromosome Mapping:   6q25.2

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 36.200000
Efficiency 96

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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