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- Tel: 858.663.9055
- Email: info@nsjbio.com
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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.
Optimal dilution of the GALT antibody should be determined by the researcher.
A recombinant human partial protein corresponding to amino acids Q188-A379 was used as the immunogen for the GALT antibody.
After reconstitution, the GALT antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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