Beta-1,3-Gal-TL Polyclonal Antibody, 50ul Primary Antibodies Bardet-Biedl syndrome is an autosomal

Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy

Classical cadherins consist of a large extracellular domain which contains DXD and DXNDN repeats responsible for mediating calcium-dependent adhesion

This gene encodes a tyrosine protein kinase

and are required for the formation of actin-based cellular protrusions

This gene is highly expressed in organs involved in lipid metabolism| and may play a role in Zellweger syndrome| in which cells are deficient in peroxisomes and have impaired bile acid synthesis

Beta-1,3-Gal-TL Polyclonal Antibody, 50ul Primary Antibodies Bardet-Biedl syndrome is an autosomalBeta 1,3 glucosyltransferase encoded by B3GALTL is a beta 1,3 glucosyltransferase that transfers glucose to O linked fucosylglycans on thrombospondin type 1 repeats (TSRs) of several proteins. The encoded protein is a type II membrane protein. Defects in this gene are a cause of Peters plus syndrome (PPS).