PrimePCR™ SYBR® Green Assay: Tiam1, Mouse

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 qMmuCIP0042267


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PrimePCR™ PreAmp for SYBR® Green Assay: Tiam1, Mouse
Reaction: 400 reactions
Gene-specific PCR primers for the unbiased preamplification of small quantities of cDNA for subsequent use in downstream gene expression analysis.

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PrimePCR™ Template for SYBR® Green Assay: Tiam1, Mouse
Reaction: 200 x 20 µl reactions desalted
Gene-specific synthetic DNA template designed to give a positive real-time PCR result when used with the corresponding primer assay.

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Assay Information

Technology:		qPCR
Assay Type:		SYBR® Green
Application:		Gene Expression
Unique Assay ID:		qMmuCID0040048
Assay Design:		Intron-spanning
Chromosome Location:		16:89793101-89794753question
Amplicon Length:		120
Splice Variants Targeted:		ENSMUST00000114122 ENSMUST00000114124 ENSMUST00000144691 ENSMUST00000164263 ENSMUST00000134021 ENSMUST00000163370 ENSMUST00000002588

Gene Information

Description Not Available

Gene Symbol:		Tiam1
Gene Name:		T cell lymphoma invasion and metastasis 1
Aliases:		AI847750, D16Ium10, D16Ium10e
RefSeq:		NC_000082.6 NT_039625.8
Ensembl:		ENSMUSG00000002489
Entrez:		21844
Chromosome Mapping:		16 C3-4\|16 61.8 cM

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 Mouse Reference Total RNA

Summary Data:

R²	0.998400
y-intercept	35.620000
Efficiency	100

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.