PrimePCR™ Probe Assay: DNASE1L3, 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:   qHsaCIP0027042
Assay Design:   Intron-spanning
Chromosome Location:   3:58183618-58186799question
Amplicon Length:   134
Splice Variants Targeted:   ENST00000450710 ENST00000318316 ENST00000486455 ENST00000483681 ENST00000477209 ENST00000394549

Gene Information

This gene encodes a member of the deoxyribonuclease I family. The encoded protein hydrolyzes DNA is not inhibited by actin and mediates the breakdown of DNA during apoptosis. Mutations in this gene are a cause of systemic lupus erythematosus-16. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq Feb 2012]

Gene Symbol:   DNASE1L3
Gene Name:   deoxyribonuclease I-like 3
Aliases:   DHP2, DNAS1L3, LSD
RefSeq:   NC_000003.11 NT_022517.18
Ensembl:   ENSG00000163687
Entrez:   1776
Chromosome Mapping:   3p14.3

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 0.999500
y-intercept 35.050000
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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