Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene.

推荐稀释比 WB:1/500-1/1000;IHC:1/50-1/100

Western blot analysis of GALT in Human fetal liver lysates using GALT antibody

Immunohistochemistry analysis of paraffin-embedded Human brain using GALT antibody. High-pressure and temperature Sodium Citrate pH 6.0 was used for antigen retrieval.

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