产品货号：
JN2020
中文名称：
重组人磷酸甘露糖变位酶2(PMM2)
英文名称：
Recombinant Human Phosphomannomutase 2
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-Ser246在C端含有His标签。
PMM2质量控制：＞95%(还原性SDS-PAGE)
PMM2制剂：液体
PMM2保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于PMM2：
Phosphomannomutase 2 (PMM2) is an enzyme that is a member of the highly variable methyltransferase superfamily. PMM2 is a cytoplasmic protein and catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate.In addition, PMM2 involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose that required for a number of critical mannosyl transfer reactions. Defects in PMM2 can results in congenital disorder of glycosylation type 1A (CDG1A). Congenital disorders of glycosylation are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation.
相关搜索：重组人磷酸甘露糖变位酶2(PMM2)，Recombinant Human Phosphomannomutase 2
PMM2质量控制：＞95%(还原性SDS-PAGE)
PMM2制剂：液体
PMM2保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于PMM2：
Phosphomannomutase 2 (PMM2) is an enzyme that is a member of the highly variable methyltransferase superfamily. PMM2 is a cytoplasmic protein and catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate.In addition, PMM2 involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose that required for a number of critical mannosyl transfer reactions. Defects in PMM2 can results in congenital disorder of glycosylation type 1A (CDG1A). Congenital disorders of glycosylation are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation.
相关搜索：重组人磷酸甘露糖变位酶2(PMM2)，Recombinant Human Phosphomannomutase 2