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- 抗原 See all COX3 (COX-3) 抗体
- COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))
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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 COX3 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 特异性
- COX3 antibody was raised against the C terminal of COX3
- 纯化方法
- Affinity purified
- 免疫原
- COX3 antibody was raised using the C terminal of COX3 corresponding to a region with amino acids FESPFTISDGIYGSTFFVATGFHGLHVIIGSTFLTICFIRQLMFHFTSKH
- Top Product
- Discover our top product COX-3 Primary Antibody
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anti-Cytochrome C Oxidase Subunit 3 (COX-3) antibody
COX-3 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Cytochrome C Oxidase Subunit 3 (COX-3) (Internal Region) antibodyCOX-3 适用: 人, 小鼠 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Cytochrome C Oxidase Subunit 3 (COX-3) (AA 182-231) antibodyCOX-3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Cytochrome C Oxidase Subunit 3 (COX-3) antibodyCOX-3 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Cytochrome C Oxidase Subunit 3 (COX-3) (AA 1-100) antibodyCOX-3 适用: 小鼠 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB: 1 µg/mL
Optimal conditions should be determined by the investigator. - 说明
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COX3 Blocking Peptide, catalog no. 33R-2880, is also available for use as a blocking control in assays to test for specificity of this COX3 antibody
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of COX3 antibody in PBS
- 浓度
- Lot specific
- 缓冲液
- PBS
- 注意事项
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Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use. - 储存条件
- 4 °C/-20 °C
- 储存方法
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
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- 抗原
- COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))
- 别名
- COX3 (COX-3 产品)
- 别名
- COIII antibody, MTCO3 antibody, cytochrome c oxidase III antibody, cytochrome c oxidase subunit III antibody, cytochrome c oxidase subunit 3 antibody, cytochrome oxidasesubunit 3 antibody, COX3 antibody, cox3 antibody
- 背景
- COX3 is a multi-pass membrane protein. It belongs to the cytochrome c oxidase subunit 3 family. Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.
- 分子量
- 29 kDa (MW of target protein)
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