PrimePCR™ SYBR® Green Assay: Tle3, 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: Recommended - best coverage; Same primer pair as used in probe assay qMmuCEP0056537


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PrimePCR™ PreAmp for SYBR® Green Assay: Tle3, 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: Tle3, 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:		qMmuCED0048111
Assay Design:		exonic
Chromosome Location:		9:61373959-61374053question
Amplicon Length:		65
Splice Variants Targeted:		ENSMUST00000159386 ENSMUST00000034820 ENSMUST00000162583 ENSMUST00000161993 ENSMUST00000160882 ENSMUST00000160724 ENSMUST00000162973 ENSMUST00000159050 ENSMUST00000160541 ENSMUST00000161207 ENSMUST00000159630 ENSMUST00000161689 ENSMUST00000178113

Gene Information

Description Not Available

Gene Symbol:		Tle3
Gene Name:		Transducin-like enhancer of split 3, homolog of Drosophila E(spl)
Aliases:		2610103N05Rik, ESG, Grg3a, Grg3b, mKIAA1547
RefSeq:		NC_000075.6 NT_039474.8
Ensembl:		ENSMUSG00000032280
Entrez:		21887
Chromosome Mapping:		9 C\|9

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 Mouse Reference Total RNA

Summary Data:

R²	0.999600
y-intercept	35.160000
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.