PrimePCR™ Probe Assay: PEPD, 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:   qHsaCEP0057528
Assay Design:   exonic
Chromosome Location:   19:33968968-33980963question
Amplicon Length:   61
Splice Variants Targeted:   ENST00000239446 ENST00000239450 ENST00000541609 ENST00000262013 ENST00000510283 ENST00000505279 ENST00000357122 ENST00000322213 ENST00000540499 ENST00000244137 ENST00000397032 ENST00000436370 ENST00000593163 ENST00000590755 ENST00000590408 ENST00000594240

Gene Information

This gene encodes a member of the peptidase family. The protein forms a homodimer that hydrolyzes dipeptides or tripeptides with C-terminal proline or hydroxyproline residues. The enzyme serves an important role in the recycling of proline and may be rate limiting for the production of collagen. Mutations in this gene result in prolidase deficiency which is characterized by the excretion of large amount of di- and tri-peptides containing proline. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq Oct 2009]

Gene Symbol:   PEPD
Gene Name:   peptidase D
Aliases:   MGC10905, PROLIDASE
RefSeq:   NC_000019.9 NG_013358.1 NT_011109.16
Ensembl:   ENSG00000124299
Entrez:   5184
Chromosome Mapping:   19q13.11

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 0.999900
y-intercept 36.520000
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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