S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Two transcript variants encoding distinct

Two transcript variants encoding distinct isoforms have been identified

Activated by intracellular alkalinization

Collagenase 3 in this family are involved in the breakdown of extracellular matrix in normal physiological processes

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S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Two transcript variants encoding distinctMutations 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.