Where to buy 6-phosphate glucose dehydrogenase (G6PD) deficiency ELISA kit?

Synonyms
G6PD, g6pd, G6pd, Dsim\G6pd, Dsim\G6pdh, G-6PD, dsim_GLEANR_8868, Dsim\GD24877, GD24877, Zw, G6PD1, G6pdx, G-6-PD, G-6-pdh, G6-pd, G6PDH, DmelCG12529, CG12529, g6pdh, MGC69058, g6pd2, fj78b06, wu:fj78b06, si:dkey-90a13.8
Description
6-phosphate glucose dehydrogenase (G6PD) deficiency is an X-linked recessive hereditary disease characterised by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH), a metabolic enzyme involved in the pentose phosphate pathway, especially important in red blood cell metabolism. Individuals with the disease may exhibit nonimmune hemolytic anemia in response to a number of causes, most commonly infection or exposure to certain medications or chemicals. G6PD deficiency is closely linked to favism, a disorder characterized by a hemolytic reaction to consumption of broad beans, with a name derived from the Italian name of the broad bean (fava). The name favism is sometimes used to refer to the enzyme deficiency as a whole, although this is misleading as not all people with G6PD deficiency will manifest a physically observable reaction to consumption of broad beans. G6PD deficiency is the most common human enzyme defect.
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