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S26A4 Polyclonal Antibody, 100ul Mammalian Expression The activity of the encoded

SKU: 36447497570

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S26A4 Polyclonal Antibody, 100ul Mammalian Expression The activity of the encodedMutations 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

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

Several human genetic disorders are caused by aberrations in human homeobox genes

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

Contains 5 C2H2-type zinc fingers

tissue specificity:Seems to be expressed in prostate and less abundantly in adult brain

S26A4 Polyclonal Antibody, 100ul Mammalian Expression The activity of the encodedMutations 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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