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S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Studies determined the encoded protein

SKU: 85920563584

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S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Studies determined the encoded proteinMutations 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.

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Description

Studies determined the encoded protein functions to prevent apoptosis and to promote cell survival

APOBEC3F is a member of the cytidine deaminase gene family

This enzyme can act as a sphingolipid delta(4)-desaturase| and also as a sphingolipid C4-hydroxylase

Activated by intracellular alkalinization

Mutations in this gene are associated with Hirschsprung disease/Mowat-Wilson syndrome

S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Studies determined the encoded proteinMutations 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.

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