NDUFAF4 抗体 (AA 101-175)
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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
- AA 101-175
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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
- 应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human NDUFAF4
- 亚型
- IgG
- Top Product
- Discover our top product NDUFAF4 Primary Antibody
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 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
- 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- NDUFAF4 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 4 (NDUFAF4))
- 别名
- NDUFAF4 (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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Synonyms: NDUF4_HUMAN, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 4, Hormone-regulated proliferation-associated protein of 20 kDa, bA22L21.1, C6orf66, HRPAP20, HSPC125, My013.
Background: 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. [provided by RefSeq, Oct 2009].
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