PrimePCR™ ddPCR™ Expression Probe Assay: SLC26A4, 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 qHsaCEP0049889; exonic

 
Fluorophore:   FAM
List Price:    $207.00
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Assay Information

Technology:   ddPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   dHsaCPE5033272
Chromosome Location:   7:107335141-107338489question
Amplicon Length:   101

Gene Information

Mutations in this gene are associated with Pendred syndrome the most common form of syndromic deafness an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq Jul 2008]

Gene Symbol:   SLC26A4
Gene Name:   solute carrier family 26, member 4
Aliases:   DFNB4, EVA, PDS, TDH2B
RefSeq:   NC_000007.13 NG_008489.1 NT_007933.15
Ensembl:   ENSG00000091137
Entrez:   5172
UniGene:   Hs.571246
Chromosome Mapping:   7q31

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