NDUFAF4 抗体 (full length)
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- 抗原 See all NDUFAF4 抗体
- NDUFAF4 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 4 (NDUFAF4))
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抗原表位
- full length
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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 NDUFAF4 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 产品特性
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Rabbit polyclonal antibody to HRPAP20 (chromosome 6 open reading frame 66)
HRPAP20 antibody [N1C3] - 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Full length human HRPAP20 Recombinant protein.
- 亚型
- IgG
- Top Product
- Discover our top product NDUFAF4 Primary Antibody
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- 应用备注
- Suggested dilution Reference Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceWestern blot1:500-1:3000*
- 说明
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Positive Control: 293T , Raji
- 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, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.
- 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
- -20 °C
- 储存方法
- Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- NDUFAF4 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 4 (NDUFAF4))
- 别名
- HRPAP20 (NDUFAF4 产品)
- 别名
- C6orf66 antibody, 1110007M04Rik antibody, 3000003G13Rik antibody, AW214064 antibody, C9H6ORF66 antibody, HRPAP20 antibody, My013 antibody, bA22L21.1 antibody, Hrpap20 antibody, NADH:ubiquinone oxidoreductase complex assembly factor 4 antibody, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 4 antibody, NDUFAF4 antibody, Ndufaf4 antibody
- 背景
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NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene are a cause of mitochondrial complex I deficiency.
Cellular Localization: Mitochondrion - 分子量
- 20 kDa
- 基因ID
- 29078
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