PrimePCR™ lncRNA SYBR® Green Assay:CACNG8, Human

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

Real-time PCR primer assay designed for SYBR® Green gene expression analysis.

Info:   Same primer pair as used in probe assay qhsaLEP0210365

List Price:    $169.00
Your Price:   Log In
Quantity:  
 
Add to Custom Plate

PrimePCR™ IncRNA PreAmp for SYBR® Green Assay: CACNG8, 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 SYBR® Green Assay: CACNG8, Human
Reaction:     4 billion copies/200 µl desalted
Gene-specific synthetic DNA template designed to give a positive real-time PCR result when used with the corresponding primer assay.


Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   lncRNA Expression
Unique Assay ID:   qhsaLED0133125
Assay Design:   exonic
Chromosome Location:   chr19:53987695-53987808question
Amplicon Length:   84
Splice Variants Targeted:   ENST00000270458
LNCipedia Splice Variants Targeted:   lnc-CACNG6-2:1

Gene Information

The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members a type II TARP and a calcium channel gamma subunit. The mRNA for this gene is believed to initiate translation from a non-AUG (CUG) start codon. [provided by RefSeq Dec 2010]

Gene Symbol:   CACNG8
Gene Name:   calcium channel, voltage-dependent, gamma subunit 8
Aliases:   FLJ16240, FLJ30598
RefSeq:   NC_000019.9 NT_011109.16
Ensembl:   ENSG00000142408
LNCipedia:   lnc-CACNG6-2
Entrez:   59283
Chromosome Mapping:   19q13.4
Gene Strand:   Not Available

Number Description Download
10039761 PrimePCR™ Assays Quick Guide, Ver B Click to download