PrimePCR™ Probe Assay: CA11, Human

RT

Real-time PCR probe assay designed for gene expression analysis. Probe assays consist of unlabeled PCR primers and a dual labeled fluorescent probe.

List Price:    $255.00
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Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCEP0049460
Assay Design:   exonic
Chromosome Location:   19:49142217-49142306question
Amplicon Length:   60
Splice Variants Targeted:   ENST00000084798 ENST00000596080

Gene Information

Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes including respiration calcification acid-base balance bone resorption and the formation of aqueous humor cerebrospinal fluid saliva and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. CA XI is likely a secreted protein however radical changes at active site residues completely conserved in CA isozymes with catalytic activity make it unlikely that it has carbonic anhydrase activity. It shares properties in common with two other acatalytic CA isoforms CA VIII and CA X. CA XI is most abundantly expressed in brain and may play a general role in the central nervous system. [provided by RefSeq Jul 2008]

Gene Symbol:   CA11
Gene Name:   carbonic anhydrase XI
Aliases:   CARPX1
RefSeq:   NC_000019.9 NT_011109.16
Ensembl:   ENSG00000063180
Entrez:   770
Chromosome Mapping:   19q13.3

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 Human Reference Total RNA

Summary Data:

R2 0.999500
y-intercept 35.940000
Efficiency 96

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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