PrimePCR™ SYBR® Green Assay: ZNF208, 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 qHsaCEP0053153

List Price:    $142.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCED0045892
Assay Design:   exonic
Chromosome Location:   19:22193619-22193741question
Amplicon Length:   93
Splice Variants Targeted:   ENST00000309683 ENST00000476120 ENST00000545510 ENST00000599916 ENST00000601773 ENST00000397126 ENST00000597040 ENST00000601993 ENST00000594710

Gene Information

Zinc finger proteins (ZNFs) such as ZNF208 bind DNA and through this binding regulate gene transcription. Most ZNFs contain conserved C2H2 motifs and are classified as Kruppel-type zinc fingers. A conserved protein motif termed the Kruppel-associated box (KRAB) domain mediates protein-protein interactions (Eichler et al. 1998 [PubMed 9724325]). See ZNF91 (MIM 603971) for further information on ZNFs.[supplied by OMIM Aug 2009]

Gene Symbol:   ZNF208
Gene Name:   zinc finger protein 208
Aliases:   PMIDP, ZNF95
RefSeq:   NC_000019.9 NT_011295.11
Ensembl:   ENSG00000160321
Entrez:   7757
UniGene:   Hs.732975
Chromosome Mapping:   19p12

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 0.999200
y-intercept 36.580000
Efficiency 98

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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