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COX3 抗体 (C-Term)

COX-3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN635599
发货至: 中国
  • 抗原 See all COX3 (COX-3) 抗体
    COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))
    抗原表位
    • 15
    • 14
    • 8
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    适用
    • 30
    • 22
    • 19
    宿主
    • 46
    • 2
    克隆类型
    • 46
    • 2
    多克隆
    标记
    • 14
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This COX3 antibody is un-conjugated
    应用范围
    • 39
    • 18
    • 13
    • 13
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    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
  • 应用备注
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    说明

    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
  • 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
    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.
  • 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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