BUD31 抗体
Quick Overview for BUD31 抗体 (ABIN7246052)
抗原
See all BUD31 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Antigen affinity purification
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免疫原
- Full length fusion protein
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亚型
- IgG
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anti-BUD31 Homolog (BUD31) (AA 1-144) antibody
BUD31 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-BUD31 Homolog (BUD31) (AA 5-54) antibodyBUD31 适用: 人, 大鼠 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-BUD31 Homolog (BUD31) (N-Term) antibodyBUD31 适用: 人, 大鼠 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-BUD31 Homolog (BUD31) (AA 35-144) antibodyBUD31 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1E10 unconjugated
anti-BUD31 Homolog (BUD31) (AA 1-144) antibodyBUD31 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-BUD31 Homolog (BUD31) (N-Term) antibodyBUD31 适用: 人, 大鼠, 小鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-BUD31 Homolog (BUD31) (N-Term) antibodyBUD31 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-BUD31 Homolog (BUD31) (AA 10-59) antibodyBUD31 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-BUD31 Homolog (BUD31) (N-Term) antibodyBUD31 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-BUD31 Homolog (BUD31) (AA 71-120) antibodyBUD31 适用: 人, 大鼠, 小鼠, Cow, 斑马鱼, 犬, 马, 兔, 豚鼠, Bat, 小鸡, Hamster, 猴, Pig, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1.5 mg/mL
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缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- BUD31 (BUD31 Homolog (BUD31))
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别名
- BUD31
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背景
- BUD31 (Protein G10 homolog, EDG-2) is a 144 amino acid protein encoded by the human gene BUD31. BUD31 is a nuclear protein that belongs to the BUD31 (G10) family. BUD31 is found on chromosome 7 which is about 158 milllion bases long, encodes over 1,000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the long (q) arm of human chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
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分子量
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Observed_MW: Refer to figures
Calculated_MW: 17 kDa
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UniProt
- P41223
抗原
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