BAZ1B 抗体
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- 抗原 See all BAZ1B 抗体
- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
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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 BAZ1B antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human BAZ1B (NP_115784.1).
- 亚型
- IgG
- Top Product
- Discover our top product BAZ1B Primary Antibody
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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
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IF(ICC) 1:50-200
IHC()
IF() - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
- 别名
- BAZ1B (BAZ1B 产品)
- 背景
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Synonyms: BAZ1B,WBSCR10,WBSCR9,WSTF
Background: This gene encodes 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.
- 基因ID
- 9031
- UniProt
- Q9UIG0
- 途径
- Nuclear Hormone Receptor Binding, Chromatin Binding
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