GALM Polyclonal Antibody, 100ul Buffer Solutions The translocation t(2

The translocation t(2

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

The encoded protein circulates in the plasma and is involved with metabolic and hormonal processes

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 The translocation t(2This 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.