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

Experience the power of LightNing™ MluI Restriction Enzymes

Melanoma inhibitory activity (cartilage-derived retinoic acid-sensitive protein (CD-RAP)

LXN encodes the only known protein inhibitor of zinc-dependent metallocarboxypeptidases

Mutations in this gene are also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lact

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.