PrimePCR™ SYBR® Green Assay: Ugt1a8, Rat

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.


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PrimePCR™ PreAmp for SYBR® Green Assay: Ugt1a8, Rat
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: Ugt1a8, Rat
Reaction: 4 billion copies/200 µl 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:		qRnoCED0001326
Assay Design:		exonic
Chromosome Location:		9:94989645-94989749question
Amplicon Length:		75
Splice Variants Targeted:		ENSRNOT00000066839 ENSRNOT00000025652 ENSRNOT00000032634 ENSRNOT00000045163 ENSRNOT00000025291 ENSRNOT00000063853 ENSRNOT00000025045 ENSRNOT00000070816 ENSRNOT00000020155 ENSRNOT00000059153

Gene Information

UDP-glucuronosyltransferase; enzyme of the glucuronidation pathway [RGD, Feb 2006]

Gene Symbol:		Ugt1a8
Gene Name:		UDP-glucuronosyltransferase 1-1
Aliases:		Not Available
RefSeq:		NM_175846
Ensembl:		ENSRNOG00000018740
Entrez:		301595
Chromosome Mapping:		9q35

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 Rat Reference Total RNA

Summary Data:

R²	0.998700
y-intercept	35.730000
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.