PrimePCR™ SYBR® Green Assay: ANXA11, 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 qHsaCIP0027088

List Price:    $142.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCID0009196
Assay Design:   Intron-spanning
Chromosome Location:   10:81921728-81923333question
Amplicon Length:   128
Splice Variants Targeted:   ENST00000372231 ENST00000422982 ENST00000438331 ENST00000372234 ENST00000360615 ENST00000265447 ENST00000535999 ENST00000537102 ENST00000424188 ENST00000372219

Gene Information

This gene encodes a member of the annexin family a group of calcium-dependent phospholipid-binding proteins. Annexins have unique N-terminal domains and conserved C-terminal domains which contain the calcium-dependent phospholipid-binding sites. The encoded protein is a 56-kD antigen recognized by sera from patients with various autoimmune diseases. Transcript variants encoding the same isoform have been identified. [provided by RefSeq Jul 2008]

Gene Symbol:   ANXA11
Gene Name:   annexin A11
Aliases:   ANX11, CAP50
RefSeq:   NC_000010.10 NT_030059.13
Ensembl:   ENSG00000122359
Entrez:   311
UniGene:   Hs.530291
Chromosome Mapping:   10q23

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 0.998000
y-intercept 35.190000
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.

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