Coagulation Factor VIII-Associated 1 (F8A1) (AA 2-80) 抗体 (Biotin)
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- 抗原 See all Coagulation Factor VIII-Associated 1 (F8A1) 抗体
- Coagulation Factor VIII-Associated 1 (F8A1)
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抗原表位
- AA 2-80
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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
- Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Mouse,Rat,Cow
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human HAP40
- 亚型
- IgG
- Top Product
- Discover our top product F8A1 Primary Antibody
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anti-Coagulation Factor VIII-Associated 1 (F8A1) (AA 171-375) antibody
F8A1 适用: 小鼠 WB, IHC, ICC 宿主: 兔 Polyclonal unconjugated
anti-Coagulation Factor VIII-Associated 1 (F8A1) (AA 150-250) antibodyF8A1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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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
- Coagulation Factor VIII-Associated 1 (F8A1)
- 别名
- HAP40/F8a (F8A1 产品)
- 别名
- DXS522E antibody, F8A antibody, HAP40 antibody, F8a antibody, Hap40 antibody, RGD1566014 antibody, f8a antibody, f8a1 antibody, hap40 antibody, dxs522e antibody, MGC147036 antibody, coagulation factor VIII associated 1 antibody, coagulation factor VIII-associated 1 antibody, coagulation factor VIII antibody, F8A1 antibody, F8a1 antibody, f8a1 antibody
- 背景
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Synonyms: Coagulation factor 8 associated intronic transcript 1, Coagulation factor VIII associated intronic transcript 1, CpG island protein, DXS522E, F8a, F8A1, F8A2, F8A3, Factor 8 associated protein, Factor 8 intron 22 protein, Factor VIII associated protein, Factor VIII intron 22 protein, huntingtin associated protein 40, F8I2_HUMAN.
Background: The Huntingtin protein contains a polyglutamine region, which leads to Huntingtin?s disease (HD) when the number of glutamine repeats exceeds thirty-five. The mutated Huntingtin protein acts within the nucleus to induce neurodegeneration by a cell-specific apoptotic mechanism. The loss of activity of the Huntingtin protein may be contributed to abnormal interactions between the mutant protein and other associated cellular proteins. Huntingtin interacts with a variety of proteins including HAP1, glyceraldehyde phosphate dehydrogenase (GAPDH), HAP40, Rab5 and HIP1. HAP40 mediates the recruitment of Huntingtin by Rab5 onto early endosomes. Specifically, this complex regulates endosome motility, which may be a key event of the pathogenetic process leading to neurodegeneration in HD.
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