Wnt-10b Monoclonal Antibody, 100ul Cell Screening and Imaging Interacts with CLTC

Interacts with CLTC

Alström syndrome

Loss of function mutations in SLC16A2 are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes

Members of this family are characterized by a highly conserved N-terminal J domain

SIRT2 encodes a member of the sirtuin family of proteins

Wnt-10b Monoclonal Antibody, 100ul Cell Screening and Imaging Interacts with CLTCThe WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It may be involved in breast cancer, and its protein signaling is likely a molecular switch that governs adipogenesis. This protein is 96%