Galectin-3 Monoclonal Antibody(8D7), 100ul Cell Function Analysis Mutations in this gene cause

Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD)

These proteins are associated with pre-mRNAs in the nucleus and regulate alternative splicing

PPP1R14C is an inhibitor of PP1

The expression of this gene is downregulated or undetectable in many cancer cell lines

Galectin-3 Monoclonal Antibody(8D7), 100ul Cell Function Analysis Mutations in this gene causeThis gene encodes a member of the galectin family of carbohydrate binding proteins. Members of this protein family have an affinity for beta galactosides. The encoded protein is characterized by an N terminal proline rich tandem repeat domain and a single C terminal carbohydrate recognition domain. This protein can self associate through the N terminal domain allowing it to bind to multivalent saccharide ligands. This protein localizes to the