PrimePCR™ SYBR® Green Assay: Tpm1, 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 qMmuCIP0042763


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PrimePCR™ PreAmp for SYBR® Green Assay: Tpm1, 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: Tpm1, 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:		qMmuCID0040546
Assay Design:		Intron-spanning
Chromosome Location:		9:67032800-67033900question
Amplicon Length:		60
Splice Variants Targeted:		ENSMUST00000113707 ENSMUST00000113705 ENSMUST00000113696 ENSMUST00000113695 ENSMUST00000034928 ENSMUST00000113690 ENSMUST00000113701 ENSMUST00000113697 ENSMUST00000113693 ENSMUST00000113689 ENSMUST00000113685 ENSMUST00000050905 ENSMUST00000113686 ENSMUST00000113687 ENSMUST00000113684 ENSMUST00000030185

Gene Information

Description Not Available

Gene Symbol:		Tpm1
Gene Name:		Tropomyosin 1, alpha
Aliases:		AA986836, AI854628, TM2, Tm3, Tmpa, Tpm-1, alpha-TM
RefSeq:		NC_000075.6 NT_039474.8
Ensembl:		ENSMUSG00000032366
Entrez:		22003
Chromosome Mapping:		9 C\|9 40.0 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	36.950000
Efficiency	97

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.