COX3 抗体 (C-Term)
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北京 101111
Quick Overview for COX3 抗体 (C-Term) (ABIN2784116)
抗原
See all COX3 (COX-3) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- C-Term
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原理
- COX3 Antibody - C-terminal region
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序列
- FESPFTISDG IYGSTFFVAT GFHGLHVIIG STFLTICFIR QLMFHFTSKH
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预测反应
- Human: 100%
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产品特性
- This is a rabbit polyclonal antibody against COX3. It was validated on Western Blot using a cell lysate as a positive control.
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纯化方法
- Affinity Purified
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免疫原
- The immunogen is a synthetic peptide directed towards the C terminal region of human COX3
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anti-Cytochrome C Oxidase Subunit 3 (COX-3) (Internal Region) antibody
COX-3 适用: 人, 小鼠 WB, IHC, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Cytochrome C Oxidase Subunit 3 (COX-3) (AA 48-77), (N-Term) antibodyCOX-3 适用: 人 WB 宿主: 兔 Polyclonal RB40383 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) (AA 1-100) antibodyCOX-3 适用: 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Cytochrome C Oxidase Subunit 3 (COX-3) (C-Term) 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
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应用备注
- Optimal working dilution should be determined by the investigator.
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说明
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP50251-100UG
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.5 mg/mL
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缓冲液
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- prevent freeze-thaw cycles
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储存条件
- 4 °C,-20 °C
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储存方法
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))
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别名
- COX3
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背景
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Background Information: 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.
Gene Name: Cytochrome c oxidase III
Alternative Symbols: COIII, MTCO3
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分子量
- 29kDa
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基因ID
- 4514
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NCBI登录号
- NP_536849
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UniProt
- P00414
抗原
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