产品货号：
JN0713
中文名称：
重组人POMGNT1(N-乙酰氨基葡萄糖-甘露糖转移酶1)
英文名称：
Recombinant Human Protein O-Linked-Mannose beta-1 2-N-Acetylglucosaminyltransferase 1
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Leu59-Thr660在C端含有His标签。
POMGNT1质量控制：＞95%(还原性SDS-PAGE)
POMGNT1制剂：液体
POMGNT1保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于POMGNT1：
Protein O-Linked-Mannose β-1 2-N-Acetylglucosaminyltransferase 1 (POMGNT1) belongs to the Glycosyltransferase 13 family. Amino acid residues between 299-311 are important for both protein expression and enzymatic activity. The minimal catalytic domain is located between positions 299-651. It is suggested that the stem domain of the soluble form is unnecessary for activity, but that some amino acids play a crucial role in the membrane-bound form. Defects in POMGNT1 are the cause of muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies type A3 (MDDGA3).
相关搜索：重组人POMGNT1(N-乙酰氨基葡萄糖-甘露糖转移酶1)
POMGNT1质量控制：＞95%(还原性SDS-PAGE)
POMGNT1制剂：液体
POMGNT1保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。
关于POMGNT1：
Protein O-Linked-Mannose β-1 2-N-Acetylglucosaminyltransferase 1 (POMGNT1) belongs to the Glycosyltransferase 13 family. Amino acid residues between 299-311 are important for both protein expression and enzymatic activity. The minimal catalytic domain is located between positions 299-651. It is suggested that the stem domain of the soluble form is unnecessary for activity, but that some amino acids play a crucial role in the membrane-bound form. Defects in POMGNT1 are the cause of muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies type A3 (MDDGA3).
相关搜索：重组人POMGNT1(N-乙酰氨基葡萄糖-甘露糖转移酶1)