PGD Polyclonal Antibody

Background:
phosphogluconate dehydrogenase(PGD) Homo sapiens 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. [provided by RefSeq, Jan 2015],

Alternative Names:
PGD, PGDH, 6-phosphogluconate dehydrogenase, decarboxylating

Immunogen: The antiserum was produced against synthesized peptide derived from human PGD. AA range:71-120

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

Observed band: 40

GeneID: PGD

Storage: -20°C/1 year

NOTE: For Research Use Only