RASSF8 抗体 (AA 101-200) (Biotin)
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- 抗原 See all RASSF8 抗体
- RASSF8 (Ras Association (RalGDS/AF-6) Domain Family (N-terminal) Member 8 (RASSF8))
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抗原表位
- AA 101-200
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适用
- 人
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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 RASSF8 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,Horse,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human RASSF8
- 亚型
- IgG
- Top Product
- Discover our top product RASSF8 Primary Antibody
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- RASSF8 (Ras Association (RalGDS/AF-6) Domain Family (N-terminal) Member 8 (RASSF8))
- 别名
- RASSF8 (RASSF8 产品)
- 别名
- c12orf2 antibody, rassf8 antibody, wu:fb96e06 antibody, zgc:64017 antibody, C12orf2 antibody, HOJ1 antibody, 5133400D11Rik antibody, AA815821 antibody, AW123240 antibody, Hoj1 antibody, mHoj-1 antibody, RGD1308820 antibody, Ras association domain family member 8 antibody, Ras association (RalGDS/AF-6) domain family (N-terminal) member 8b antibody, Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 antibody, RASSF8 antibody, rassf8b antibody, Rassf8 antibody
- 背景
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Synonyms: HOJ1, C12orf2, Ras association domain-containing protein 8, Carcinoma-associated protein HOJ-1, RASSF8
Background: This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t(12,22)(p11.2,q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
- 基因ID
- 11228
- UniProt
- Q8NHQ8
- 途径
- Chromatin Binding
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