BUD31 抗体
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- 抗原 See all BUD31 抗体
- BUD31 (BUD31 Homolog (BUD31))
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适用
- 人, 大鼠, 小鼠
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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 BUD31 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Antigen affinity purification
- 免疫原
- Full length fusion protein
- 亚型
- IgG
- Top Product
- Discover our top product BUD31 Primary Antibody
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- 应用备注
- WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1.5 mg/mL
- 缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 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 -20°C. Avoid freeze / thaw cycles.
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- 抗原
- BUD31 (BUD31 Homolog (BUD31))
- 别名
- BUD31 (BUD31 产品)
- 别名
- Cwc14 antibody, EDG-2 antibody, EDG2 antibody, G10 antibody, YCR063W antibody, fSAP17 antibody, g10l antibody, zgc:110615 antibody, CWC14 antibody, DDBDRAFT_0190998 antibody, DDBDRAFT_0233523 antibody, DDB_0190998 antibody, DDB_0233523 antibody, bud31 antibody, Edg2 antibody, C77604 antibody, g10 antibody, c77604 antibody, BUD31 homolog antibody, BUD31 homolog (S. cerevisiae) antibody, protein BUD31 homolog antibody, U2 snRNP complex subunit BUD31 antibody, U2 snRNP complex subunit antibody, hypothetical protein antibody, BUD31 homolog (yeast) antibody, BUD31 homolog L homeolog antibody, maternal g10 transcript antibody, Protein BUD31 homolog antibody, BUD31 antibody, bud31 antibody, Bud31 antibody, bud31.L antibody, LOC5569643 antibody, CC1G_08861 antibody, bud-31 antibody, LOC109464260 antibody, LOC108703088 antibody
- 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.
- 分子量
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Observed_MW: Refer to figures
Calculated_MW: 17 kDa
- UniProt
- P41223
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