SYBR Green qPCR primers for detecting human SLC26A4 (solute carrier family 26 member 4) gene expression by real-time PCR. Each set comes with primer sequences and reaction conditions.
Human SLC26A4 qPCR Primer Set – solute carrier family 26 member 4
Also known as: DFNB4, EVA, PDS, TDH2B
About this gene: Mutations in SLC26A4 are linked to Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. The SLC26A4 gene product is highly homologous to the SLC26A3 gene; they have similar genomic structures and SLC26A4 is located 3' of the SLC26A3 gene. The SLC26A4 protein has homology to sulfate transporters.
Gene details: NCBI Gene ID: 5172; HGNC ID: HGNC:8818; UniProt: O43511; RefSeq (MANE Select): NM_000441.2; Chromosome location: 7q22.3
What you get: Primers are provided as a 40 µl solution containing both primers at a final concentration of 50 µM in 10 mM Tris-HCl (pH 7.5), 0.1 mM EDTA. Dilute with H2O as needed prior to use. This amount is sufficient for 1,000 PCR reactions of 20 µl, assuming a final primer concentration of 0.1 µM.
Browse all Human PCR Primer Sets.