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)