PrimePCR™ SYBR® Green Assay: CFLAR, 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 qHsaCIP0041627

List Price:    $146.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCID0038905
Assay Design:   Intron-spanning
Chromosome Location:   2:201997826-202000808question
Amplicon Length:   116
Splice Variants Targeted:   ENST00000309955 ENST00000443227 ENST00000341222 ENST00000341582 ENST00000342795 ENST00000395148 ENST00000423241 ENST00000440180 ENST00000457277 ENST00000494258 ENST00000470178 ENST00000462763 ENST00000479953 ENST00000355558 ENST00000340870

Gene Information

The protein encoded by this gene is a regulator of apoptosis and is structurally similar to caspase-8. However the encoded protein lacks caspase activity and appears to be itself cleaved into two peptides by caspase-8. Several transcript variants encoding different isoforms have been found for this gene and partial evidence for several more variants exists. [provided by RefSeq Feb 2011]

Gene Symbol:   CFLAR
Gene Name:   CASP8 and FADD-like apoptosis regulator
Aliases:   CASH, CASP8AP1, CLARP, Casper, FLAME, FLAME-1, FLAME1, FLIP, I-FLICE, MRIT, c-FLIP, c-FLIPL, c-FLIPR, c-FLIPS
RefSeq:   NC_000002.11 NT_005403.17
Ensembl:   ENSG00000003402
Entrez:   8837
UniGene:   Hs.390736
Chromosome Mapping:   2q33-q34

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 0.999400
y-intercept 36.820000
Efficiency 94

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.

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