TTPA 抗体 (C-Term)
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- 抗原 See all TTPA 抗体
- TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))
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抗原表位
- C-Term
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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 TTPA antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- Hamster, 人, 小鼠, 大鼠
- 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human alpha TTP. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product TTPA Primary Antibody
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- 应用备注
- WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
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Positive Control: IMR32 , mouse liver , rat liver
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))
- 别名
- alpha tocopherol transfer protein (TTPA 产品)
- 别名
- ATTP antibody, AVED antibody, TTP1 antibody, alphaTTP antibody, TTP antibody, alpha-TTP antibody, alpha tocopherol transfer protein antibody, tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency) antibody, tocopherol (alpha) transfer protein antibody, TTPA antibody, ttpa antibody, Ttpa antibody
- 背景
- Alpha tocopherol transfer protein , ATTP , AVED , TTP1 , alphaTTP,This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa. [provided by RefSeq]
- 分子量
- 32 kDa
- 基因ID
- 7274
- UniProt
- P49638
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