PrimePCR™ SYBR® Green Assay: LPGAT1, 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 qHsaCIP0029544


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PrimePCR™ PreAmp for SYBR® Green Assay: LPGAT1, Human
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: LPGAT1, Human
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:		qHsaCID0014761
Assay Design:		Intron-spanning
Chromosome Location:		1:211966467-212002510question
Amplicon Length:		146
Splice Variants Targeted:		ENST00000366997 ENST00000366996

Gene Information

Acyl-CoA:lysophosphatidylglycerol (LPG) acyltransferase catalyzes the reacylation of LPG to phosphatidylglycerol a membrane phospholipid that is an important precursor for the synthesis of cardiolipin (Yang et al. 2004 [PubMed 15485873]).[supplied by OMIM Mar 2008]

Gene Symbol:		LPGAT1
Gene Name:		lysophosphatidylglycerol acyltransferase 1
Aliases:		FAM34A, FAM34A1, NET8
RefSeq:		NC_000001.10 NT_167186.1
Ensembl:		ENSG00000123684
Entrez:		9926
Chromosome Mapping:		1q32

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 Human Reference Total RNA

Summary Data:

R²	0.999900
y-intercept	35.350000
Efficiency	99

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.