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WFS1 Polyclonal Antibody, 20ul Cell Screening and Imaging Experience the power of LightNing™

SKU: 6746892857

4.8
USD97.20 USD128.20

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WFS1 Polyclonal Antibody, 20ul Cell Screening and Imaging Experience the power of LightNing™This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system.

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Description

Experience the power of LightNing™ MluI Restriction Enzymes

It is not active until the last two amino acids of the carboxy-terminus have been cleaved off

a member of the epidermal growth factor receptor family of receptor tyrosine kinases

The active site residues of carboxypeptidases A and B are conserved in this protein

The enzyme encoded by this gene is a type I gamma-glutamyltransferase that catalyzes the transfer of the glutamyl moiety of glutathione to a variety of amino acids and dipeptide acceptors

WFS1 Polyclonal Antibody, 20ul Cell Screening and Imaging Experience the power of LightNing™This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system.

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