PMM2 抗体
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- 抗原 See all PMM2 抗体
- PMM2 (Phosphomannomutase 2 (PMM2))
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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 PMM2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- 纯化方法
- Immunogen affinity purified
- 纯度
- ≥95 % as determined by SDS-PAGE
- 免疫原
- phosphomannomutase 2
- 亚型
- IgG
- Top Product
- Discover our top product PMM2 Primary Antibody
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anti-Phosphomannomutase 2 (PMM2) (AA 1-246) antibody
PMM2 适用: 人 WB, IHC, ELISA, IP 宿主: 兔 Polyclonal unconjugated
anti-Phosphomannomutase 2 (PMM2) (AA 47-111) antibodyPMM2 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Phosphomannomutase 2 (PMM2) antibodyPMM2 适用: 人, 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Phosphomannomutase 2 (PMM2) (AA 47-111) antibodyPMM2 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2E9 unconjugated
anti-Phosphomannomutase 2 (PMM2) (C-Term) antibodyPMM2 适用: 人, 小鼠, 大鼠 WB, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Phosphomannomutase 2 (PMM2) (AA 1-246) antibodyPMM2 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2A5 unconjugated
anti-Phosphomannomutase 2 (PMM2) (AA 1-246) antibodyPMM2 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Phosphomannomutase 2 (PMM2) antibodyPMM2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Phosphomannomutase 2 (PMM2) (AA 1-246) antibodyPMM2 适用: 人 IP 宿主: 兔 Polyclonal unconjugated
anti-Phosphomannomutase 2 (PMM2) (AA 1-246) antibodyPMM2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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- 应用备注
- WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide and 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
- -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
- 有效期
- 12 months
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- 抗原
- PMM2 (Phosphomannomutase 2 (PMM2))
- 别名
- PMM2 (PMM2 产品)
- 背景
- Synonyms: Background:The protein encoded by this gene catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate, which is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides. Mutations in this gene have been shown to cause defects in glycoprotein biosynthesis, which manifests as carbohydrate-deficient glycoprotein syndrome type I.
- 分子量
- 28 kDa
- 基因ID
- 5373
- UniProt
- O15305
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