GPNMB Polyclonal Antibody, 50ul Pipette Filler Defects in protein kinase C

Defects in protein kinase C gamma have been associated with neurodegenerative disorder spinocerebellar ataxia-14 (SCA14)

It also interacts with Src family protein-tyrosine kinases in a phosphorylation-dependent manner| suggesting that this protein may function in cell-cell adhesion as well as in cellular signaling

SLC3A2 is a member of the solute carrier family and encodes a cell surface

3 kb is more widel

Binds to pre-mRNA in spliceosome C complex

GPNMB Polyclonal Antibody, 50ul Pipette Filler Defects in protein kinase CThe protein encoded by this gene is a type I transmembrane glycoprotein which shows homology to the pMEL17 precursor, a melanocyte specific protein. GPNMB shows expression in the lowly metastatic human melanoma cell lines and xenografts but does not show expression in the highly metastatic cell lines. GPNMB may be involved in growth delay and reduction of metastatic potential. Two transcript variants encoding different isoforms have been found for