PrimePCR™ lncRNA® Probe Assay:SCN5A, Human

PrimePCR Primer Assays for Real-Time PCR oligo primer pair tube for SYBR Green gene expression.

Real-time PCR probe assay designed for gene expression analysis. Probe assays consist of unlabeled PCR primers and a dual labeled fluorescent probe.

Info:   Same primer pair as used in SYBR assay qhsaLED0104401

List Price:    $247.00
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PrimePCR™ IncRNA PreAmp for Probe Assay: SCN5A, Human
Reaction:     400 reactions
Gene-specific PCR primers for the unbiased preamplification of small quantities of cDNA for subsequent use in downstream gene expression analysis.

PrimePCR™ IncRNA Template for Probe Assay: SCN5A, Human
Reaction:     4 billion copies/200 µl
Gene-specific synthetic DNA template designed to give a positive real-time PCR result when used with the corresponding probe assay.


Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   lncRNA Expression
Unique Assay ID:   qhsaLEP0181641
Assay Design:   exonic
Chromosome Location:   chr3:38614052-38620958question
Amplicon Length:   100
Refseq Transcripts Amplified:   XM_017007017,XM_011533991,NM_001160161,NM_001160160,NM_000335,NM_198056,NM_001099405,NM_001099404
Splice Variants Targeted:   ENST00000455624 ENST00000449557 ENST00000612060 ENST00000423572 ENST00000333535 ENST00000425664 ENST00000413689 ENST00000451551 ENST00000491944 ENST00000414099 ENST00000450102
LNCipedia Splice Variants Targeted:   lnc-SCN10A-1:1

Gene Information

The protein encoded by this gene is an integral membrane protein and tetrodotoxin-resistant voltage-gated sodium channel subunit. This protein is found primarily in cardiac muscle and is responsible for the initial upstroke of the action potential in an electrocardiogram. Defects in this gene are a cause of long QT syndrome type 3 (LQT3) an autosomal dominant cardiac disease. Alternative splicing results in several transcript variants encoding different isoforms. [provided by RefSeq Jul 2008]

Gene Symbol:   SCN5A
Gene Name:   sodium channel, voltage-gated, type V, alpha subunit
Aliases:   CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD, HH1, ICCD, IVF, LQT3, Nav1.5, PFHB1, SSS1, VF1
RefSeq:   NC_000003.11 NT_022517.18 NG_008934.1
Ensembl:   ENSG00000183873
LNCipedia:   lnc-SCN10A-1
Entrez:   6331
Chromosome Mapping:   3p21
Gene Strand:   Not Available

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