G6PD polyclonal, anti-human

Background:
Glucose-6-phosphate 1-dehydrogenase (G6PD) plays an important role in the pentose phosphate pathway. It is a member of the glucose-6-phosphate dehydrogenase family of proteins. G6PD is a ubiquitous enzyme that produces pentose sugars for nucleic acid synthesis, but is also involved in carbohydrate degradation, as it is one of the main producers of NADPH reducing power. G6PD has NADP as a co-factor and structural element. It can be found as a homodimer or homotetramer, and is primarily detected in lymphoblasts, granulocytes and sperm. Defects in G6PD can cause chronic non-spherocytic hemolytic anemia (CNSHA), especially in areas in which malaria is an epidemic. Individuals with a high level of G6PD-deficiency are at higher risk of acute hemolytic attacks.

Alternative Name:
G6PD, G6PD, G6PD, G6PD1, G6pdx, Glucose 6 phosphate 1 dehydrogenase, Glucose 6 phosphate dehydrogenase, Glucose 6 phosphate dehydrogenase, G6PD, Glucose-6-phosphate 1-dehydrogenase, MET19, POS10, Zwf1p,

Application Dilution:
WB:1:500-1:2,000
ICC:1:50-1:200
IHC:1:50-1:200
FC:1:50-1:100

Specificity: G6PD polyclonal antibody detects endogenous levels of G6PD protein.

Immunogen:
recombinant protein

MW: 59 kDa

Swiss-Prot: P11413(Human)

Purification & Purity:
ProA affinity purified

Format:
Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2

Storage:
Store at +4°C after thawing. Aliquot store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

For research use only, not for use in diagnostic procedure.