PrimePCR™ ddPCR™ Expression Probe Assay: MYO15A, Human

PrimePCR

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

Info:   FAM; Same primer pair and probe as used in qPCR assay qHsaCEP0049898; exonic

 
Fluorophore:   FAM
List Price:    $207.00
Your Price:   Log In
 

Assay Information

Technology:   ddPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   dHsaCPE5033290
Chromosome Location:   17:18064651-18064741question
Amplicon Length:   61

Gene Information

This gene encodes an unconventional myosin. This protein differs from other myosins in that it has a long N-terminal extension preceding the conserved motor domain. Studies in mice suggest that this protein is necessary for actin organization in the hair cells of the cochlea. Mutations in this gene have been associated with profound congenital neurosensory nonsyndromal deafness. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Read-through transcripts containing an upstream gene and this gene have been identified but they are not thought to encode a fusion protein. Several alternatively spliced transcript variants have been described but their full length sequences have not been determined. [provided by RefSeq Jul 2008]

Gene Symbol:   MYO15A
Gene Name:   myosin XVA
Aliases:   DFNB3, DKFZp686N18198, FLJ17274, FLJ31311, MYO15
RefSeq:   NC_000017.10 NG_011634.1 NT_010718.16
Ensembl:   ENSG00000091536
Entrez:   51168
UniGene:   Hs.462390
Chromosome Mapping:   17p11.2

Number Description Download