PrimePCR™ SYBR® Green Assay: CIT, 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:   Recommended - best coverage; Same primer pair as used in probe assay qHsaCEP0051230

List Price:    $142.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCED0043968
Assay Design:   exonic
Chromosome Location:   12:120171993-120172139question
Amplicon Length:   117
Splice Variants Targeted:   ENST00000392521 ENST00000261833 ENST00000392520 ENST00000546026

Gene Information

This gene encodes a serine/threonine-protein kinase that functions in cell division. Together with the kinesin KIF14 this protein localizes to the central spindle and midbody and functions to promote efficient cytokinesis. This protein is involved in central nervous system development. Polymorphisms in this gene are associated with bipolar disorder and risk for schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq Aug 2011]

Gene Symbol:   CIT
Gene Name:   citron (rho-interacting, serine/threonine kinase 21)
Aliases:   CRIK, KIAA0949, STK21
RefSeq:   NC_000012.11 NT_009775.17
Ensembl:   ENSG00000122966
Entrez:   11113
UniGene:   Hs.119594
Chromosome Mapping:   12q24

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 0.999700
y-intercept 36.200000
Efficiency 95

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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