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- Tel: 858.663.9055
- Email: info@nsjbio.com
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6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene.
Optimal dilution of the PGDH antibody should be determined by the researcher.
An E.coli-derived human recombinant protein (amino acids D24-R447) was used as the immunogen for the PGDH antibody.
After reconstitution, the PGDG 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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