PrimePCR™ Probe Assay: ZNF397, 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.

Info:   Recommended - best efficiency

List Price:    $255.00
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Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCEP0058577
Assay Design:   exonic
Chromosome Location:   18:32822747-32822847question
Amplicon Length:   71
Splice Variants Targeted:   ENST00000601719 ENST00000591206 ENST00000330501 ENST00000261333 ENST00000355632 ENST00000585800 ENST00000592264 ENST00000588119

Gene Information

This gene encodes a protein with a N-terminal SCAN domain and the longer isoform contains nine C2H2-type zinc finger repeats in the C-terminal domain. The protein localizes to centromeres during interphase and early prophase and different isoforms can repress or activate transcription in transfection studies. Multiple transcript variants encoding different isoforms have been found for this gene. Additional variants have been described but their biological validity has not been determined. [provided by RefSeq Oct 2009]

Gene Symbol:   ZNF397
Gene Name:   zinc finger protein 397
Aliases:   MGC13250, ZNF47, ZSCAN15
RefSeq:   NC_000018.9 NT_010966.14 NG_015815.1
Ensembl:   ENSG00000186812
Entrez:   84307
Chromosome Mapping:   18q12.2

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 0.999300
y-intercept 35.640000
Efficiency 103

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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