PrimePCR™ Probe Assay: PARK2, 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:   qHsaCIP0039629
Assay Design:   Intron-spanning
Chromosome Location:   6:162206852-162394394question
Amplicon Length:   120
Splice Variants Targeted:   ENST00000366898 ENST00000366897 ENST00000366896 ENST00000366894 ENST00000338468 ENST00000366892

Gene Information

The precise function of this gene is unknown; however the encoded protein is a component of a multiprotein E3 ubiquitin ligase complex that mediates the targeting of substrate proteins for proteasomal degradation. Mutations in this gene are known to cause Parkinson disease and autosomal recessive juvenile Parkinson disease. Alternative splicing of this gene produces multiple transcript variants encoding distinct isoforms. Additional splice variants of this gene have been described but currently lack transcript support. [provided by RefSeq Jul 2008]

Gene Symbol:   PARK2
Gene Name:   parkinson protein 2, E3 ubiquitin protein ligase (parkin)
Aliases:   AR-JP, LPRS2, PDJ, PRKN
RefSeq:   NG_011525.1 NC_000006.11 NG_008289.1 NT_025741.15
Ensembl:   ENSG00000185345
Entrez:   5071
Chromosome Mapping:   6q25.2-q27

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 0.999700
y-intercept 36.050000
Efficiency 97

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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