• 靶点：
• ALG1

• 简介：
• >>N-Glycan biosynthesis;>>Various types of N-glycan biosynthesis;>>Metabolic pathways

• 基因名称：
• ALG1 HMAT1 HMT1 PSEC0061 UNQ861/PRO1870

• 蛋白名称：
• ALG1

• Human Gene Id：
• 56052

• Human Swiss Prot No：
• Q9BT22

• Mouse Gene Id：
• 208211

• Mouse Swiss Prot No：
• Q921Q3

• 免疫原：
• Synthesized peptide derived from human ALG1 AA range: 180-230

• 特异性：
• This antibody detects endogenous levels of ALG1 at Human/Mouse

• 组成：
• Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

• 来源：
• Polyclonal, Rabbit,IgG

• 稀释：
• WB 1：500-2000

• 纯化工艺：
• The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

• 浓度：
• 1 mg/ml

• 储存：
• -15°C to -25°C/1 year(Do not lower than -25°C)

• 分子量：
• 51kD

• 背景：
• The enzyme encoded by this gene catalyzes the first mannosylation step in the biosynthesis of lipid-linked oligosaccharides. This gene is mutated in congenital disorder of glycosylation type Ik. [provided by RefSeq, Dec 2008],

• 功能：
• catalytic activity:GDP-mannose + chitobiosyldiphosphodolichol = GDP + beta-1,4-D-mannosylchitobiosyldiphosphodolichol.,disease:Defects in ALG1 are the cause of congenital disorder of glycosylation type 1K (CDG1K) [MIM:608540]. CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.,function:Participates in the formation of the lipid-linked precursor oligosaccharide for N-glycosylation. Involved in assembli

• 细胞定位：
• Endoplasmic reticulum membrane ; Single-pass type II membrane protein .

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