PrimePCR™ Probe Assay: PXDN, 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:   qHsaCIP0026399
Assay Design:   Intron-spanning
Chromosome Location:   2:1684094-1687869question
Amplicon Length:   100
Splice Variants Targeted:   ENST00000252804 ENST00000433670 ENST00000447941 ENST00000425171

Gene Information

Drosophila peroxidasin is an extracellular matrix-associated peroxidase (Horikoshi et al. 1999 [PubMed 10441517]). It is expressed exclusively in hemocytes derived from head mesoderm at a very early stage of differentiation. Peroxidasin exists as a homotrimer with a unique hybrid structure that combines an enzymatically functional peroxidase domain with motifs that are typically found in extracellular matrix-associated proteins. It is a secreted protein that contains a secretory recognition sequence at its N terminus. Peroxidasin catalyzes hydrogen peroxide-driven radioiodination oxidations and the formation of dityrosine in vitro. It is also thought to function in extracellular matrix consolidation phagocytosis and defense.[supplied by OMIM Jul 2009]

Gene Symbol:   PXDN
Gene Name:   peroxidasin homolog (Drosophila)
Aliases:   D2S448, D2S448E, KIAA0230, MG50, PRG2, PXN, VPO
RefSeq:   NC_000002.11 NT_022221.13
Ensembl:   ENSG00000130508
Entrez:   7837
Chromosome Mapping:   2p25

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 0.999400
y-intercept 34.970000
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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