BAZ1B 抗体 (N-Term)
(1 reference)Quick Overview for BAZ1B 抗体 (N-Term) (ABIN965640)
抗原
See all BAZ1B 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- N-Term
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纯化方法
- Purified by antigen-specific affinity chromatography.
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免疫原
- Polyclonal antibody produced in rabbits immunizing with a synthetic peptide corresponding to N-terminal residues of human BAZ1B (bromodomain adjacent to zinc finger domain, 1B)
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anti-Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B) (AA 1-260) antibody
BAZ1B 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B) (AA 1384-1483) antibodyBAZ1B 适用: 人 ELISA, IHC (p), PLA 宿主: 小鼠 Monoclonal 5E9 unconjugated
anti-Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B) (AA 1384-1484) antibodyBAZ1B 适用: 人 ELISA, IHC, IHC (p) 宿主: 小鼠 Monoclonal 5E9 unconjugated
anti-Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B) antibodyBAZ1B 适用: 人 WB, FACS, ICC, DB 宿主: 小鼠 Monoclonal BAZ1H4H9 unconjugated
anti-Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B) (AA 1384-1483) antibodyBAZ1B 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B) (C-Term) antibodyBAZ1B 适用: 人, 小鼠, 大鼠, 犬, 豚鼠, 马 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- ELISA, Western blotting: 1µg/ml for 2hrs.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- This antibody is stored in PBS, 50% glycerol
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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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: "A novel human gene, WSTF, is deleted in Williams syndrome." in: Genomics, Vol. 54, Issue 2, pp. 241-9, (1999) (PubMed).
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: "A novel human gene, WSTF, is deleted in Williams syndrome." in: Genomics, Vol. 54, Issue 2, pp. 241-9, (1999) (PubMed).
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- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
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别名
- BAZ1B
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背景
- The BAZ1B (bromodomain adjacent to zinc finger domain, 1B) is a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing of this gene generates at least 2 transcript variants.
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途径
- Nuclear Hormone Receptor Binding, Chromatin Binding
抗原
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