PGD Mouse Monoclonal Antibody [Kloon ID: LBI2A5]

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. [provided by RefSeq]

Carrier-free (BSA/glycerol-free) PGD mouse monoclonal antibody, clone LBI2A5

6PGD

Homo sapiens phosphogluconate dehydrogenase (PGD), transcript variant 1, mRNA.

5226

P52209

Unconjugated

Glutathione metabolism, Metabolic pathways, Pentose phosphate pathway

Glutathione metabolism, Metabolic pathways, Pentose phosphate pathway

WB 1:2000, IHC 1:150, IF 1:100

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

PGD

https://www.ncbi.nlm.nih.gov/gene/?term=5226

https://www.uniprot.org/uniprot/P52209