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- 抗原 See all MAN1B1 抗体
- MAN1B1 (Mannosidase, Alpha, Class 1B, Member 1 (MAN1B1))
- 适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This MAN1B1 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human MAN1B1
- 亚型
- IgG
- Top Product
- Discover our top product MAN1B1 Primary Antibody
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anti-Mannosidase, Alpha, Class 1B, Member 1 (MAN1B1) (AA 112-211) antibody
MAN1B1 适用: 人 WB, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 6B1 unconjugated
anti-Mannosidase, Alpha, Class 1B, Member 1 (MAN1B1) (Internal Region) antibodyMAN1B1 适用: 人, 小鼠, 大鼠 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Mannosidase, Alpha, Class 1B, Member 1 (MAN1B1) (Internal Region) antibodyMAN1B1 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500 - 1:2000
- 说明
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Widely expressed
- 限制
- 仅限研究用
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- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20C. Avoid freeze / thaw cycles.
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- 抗原
- MAN1B1 (Mannosidase, Alpha, Class 1B, Member 1 (MAN1B1))
- 别名
- MAN1B1 (MAN1B1 产品)
- 别名
- erman1 antibody, mana-er antibody, MAN1B1 antibody, ERMAN1 antibody, MANA-ER antibody, MRT15 antibody, E430019H13Rik antibody, ERMan1 antibody, Gm108 antibody, RGD1563595 antibody, mannosidase alpha class 1B member 1 antibody, mannosidase, alpha, class 1B, member 1 L homeolog antibody, endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase antibody, mannosidase, alpha, class 1B, member 1 antibody, MAN1B1 antibody, man1b1.L antibody, LOC480667 antibody, man1b1 antibody, Man1b1 antibody
- 背景
- This gene encodes an enzyme belonging to the glycosyl hydrolase 47 family. This enzyme functions in N-glycan biosynthesis, and is a class I alpha-1,2-mannosidase that specifically converts Man9GlcNAc to Man8GlcNAc isomer B. It is required for N-glycan trimming to Man5-6GlcNAc2 in the endoplasmic-reticulum-associated degradation pathway. Mutations in this gene cause autosomal-recessive intellectual disability. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 11.
- 分子量
- 79.58 kDa
- 基因ID
- 11253
- UniProt
- Q9UKM7
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