产品货号：
JN1271
中文名称：
重组人PGD(6-磷酸葡萄糖酸脱氢酶)
英文名称：
Recombinant Human 6-phosphogluconate dehydrogenase
产品规格：
10μg|50μg|500μg|1mg
发货周期：
1～3天
产品价格：
询价
本品由我们的哺乳动物细胞表达系统制备而成，目的基因编码的Met1-Ala483在C端含有His标签。
PGD质量控制：＞95%(还原性SDS-PAGE)
PGD制剂：液体
PGD保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于PGD：
6-phosphogluconate dehydrogenase(PGD) is a cytoplasm-located protein, and belongs to the 6-phosphogluconate dehydrogenase family. 6PGD is the second dehydrogenase in the pentose phosphate shunt. It catalyzes the oxidative decarboxylation of 6-phosphogluconate to ribulose 5-phosphate and CO2, with concomitant reduction of NADP to NADPH. Mutations within the gene coding this enzyme result in 6-phosphogluconate dehydrogenase deficiency, an autosomal hereditary disease effecting the red blood cells.
相关搜索：重组人PGD(6-磷酸葡萄糖酸脱氢酶)
PGD质量控制：＞95%(还原性SDS-PAGE)
PGD制剂：液体
PGD保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于PGD：
6-phosphogluconate dehydrogenase(PGD) is a cytoplasm-located protein, and belongs to the 6-phosphogluconate dehydrogenase family. 6PGD is the second dehydrogenase in the pentose phosphate shunt. It catalyzes the oxidative decarboxylation of 6-phosphogluconate to ribulose 5-phosphate and CO2, with concomitant reduction of NADP to NADPH. Mutations within the gene coding this enzyme result in 6-phosphogluconate dehydrogenase deficiency, an autosomal hereditary disease effecting the red blood cells.
相关搜索：重组人PGD(6-磷酸葡萄糖酸脱氢酶)