CD58 Polyclonal Antibody, 50ul[BT-AP02361] Cell Labeling & Imaging Mutations in this gene are

Mutations in this gene are the cause of certain genetically-related cataract disorders

cell motility and morphogenesis in numerous cell and tissue types

Multiple alternatively spliced transcript variants have been found for PFKFB1

5'-triiodothyronine (RT3) and 3

GPIb alpha chain provides the VWF binding site

CD58 Polyclonal Antibody, 50ul[BT-AP02361] Cell Labeling & Imaging Mutations in this gene areCNNM2 encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play an important role in magnesium homeostasis by mediating the epithelial transport and renal reabsorption of Mg2+. Mutations in CNNM2 are associated with renal hypomagnesemia. Alternatively spliced transcript variants encoding multiple