产品货号：
JN0888
中文名称：
重组人半乳糖激酶(Galactokinase)
英文名称：
Recombinant Human Galactokinase
产品规格：
10μg|50μg|500μg|1mg
发货周期：
1～3天
产品价格：
询价
本品由我们的大肠杆菌表达系统制备而成，目的基因编码的Met1-Leu392在C端含有His标签。
Galactokinase质量控制：＞95%(还原性SDS-PAGE)
Galactokinase制剂：液体
Galactokinase保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于Galactokinase：
Galactokinase belongs to the GHMP kinase family and GalK subfamily. Galactokinase is more important to the galactose metabolism pathway. It modifies galactose to create a similar molecule called Galactose-1-Phosphate.Thus, a series of additional steps converts Galactose-1-Phosphate to another simple sugar Glucose, which is the main energy source for most cells. Galactokinase deficiency results in Galactosemia II, an autosomal recessive deficiency characterized by congenital cataracts during infancy and presenile cataracts in the adult population. The cataracts are secondary to accumulation of Galactitol in the lenses.
相关搜索：重组人半乳糖激酶(Galactokinase)，Recombinant Human Galactokinase
Galactokinase质量控制：＞95%(还原性SDS-PAGE)
Galactokinase制剂：液体
Galactokinase保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于Galactokinase：
Galactokinase belongs to the GHMP kinase family and GalK subfamily. Galactokinase is more important to the galactose metabolism pathway. It modifies galactose to create a similar molecule called Galactose-1-Phosphate.Thus, a series of additional steps converts Galactose-1-Phosphate to another simple sugar Glucose, which is the main energy source for most cells. Galactokinase deficiency results in Galactosemia II, an autosomal recessive deficiency characterized by congenital cataracts during infancy and presenile cataracts in the adult population. The cataracts are secondary to accumulation of Galactitol in the lenses.
相关搜索：重组人半乳糖激酶(Galactokinase)，Recombinant Human Galactokinase