Beta-1,4-Gal-T5 Polyclonal Antibody, 20ul Immunoassays an autosomal recessive disorder characterized

an autosomal recessive disorder characterized by palmoplantar keratosis and periodontitis

this complex is required for nonhomologous joining of DNA ends and possesses increased single-stranded DNA endonuclease and 3' to 5' exonuclease activities

this protein induces ectopic bone formation and may promote fracture healing in human patients

1 μm pore size and a 75 mm diameter PES membrane

it enhanced transcription from a nuclear factor kappa-B (NFKB)-dependent reporter gene

Beta-1,4-Gal-T5 Polyclonal Antibody, 20ul Immunoassays an autosomal recessive disorder characterizedB4GALT5 is one of seven beta 1,4 galactosyltransferase (beta4GalT) genes. They encode type II membrane bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP galactose; all transfer galactose in a beta1,4 linkage to similar acceptor sugars: glcNAc, Glc, and Xyl. Each beta4GalT has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have an