S26A4 rabbit pAb
Ref. EK-ES11814
50µl
188.00€
100µl
316.00€
Product Information
Name:S26A4 rabbit pAb
Brand:ELK Biotechnology
Description: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],
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Chemical properties
Technical inquiry about: S26A4 rabbit pAb
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