GALM Polyclonal Antibody, 100ul Buffer Solutions |Can degrade fibrillar type I|

|Can degrade fibrillar type I| II| and III collagens

The mechanisms of dishevelled function in Wnt signaling are likely to be conserved among metazoans

covalently bound through di-sulfide bonds to one of several possible light chains

Mutations in this gene cause nephronophthisis (NPHP)| an autosomal recessive kidney disease characterized by tubular basement membrane disruption| interstitial lymphohistiocytic cell infiltration| and development of cysts at the corticomedullary border of the kidneys

GALM Polyclonal Antibody, 100ul Buffer Solutions |Can degrade fibrillar type I|This gene encodes an enzyme that catalyzes the epimerization of hexose sugars such as glucose and galactose. The encoded protein is expressed in the cytoplasm and has a preference for galactose. The encoded protein may be required for normal galactose metabolism by maintaining the equilibrium of alpha and beta anomers of galactose.