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S26A4 Polyclonal Antibody, 100ul Mammalian Expression Not detected in brain and

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S26A4 Polyclonal Antibody, 100ul Mammalian Expression Not detected in brain andMutations 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

Not detected in brain and skeletal muscle

The activity of the encoded protein is regulated by polo-like kinase 1

This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) subfamily of nuclear receptors

The protein may play a role in the adhesive interactions of activated T and NK cells during the late phase of the immune response

S26A4 Polyclonal Antibody, 100ul Mammalian Expression Not detected in brain andMutations 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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