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COA5 Protein (Myc-DYKDDDDK Tag)

COA5 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2714096
发货至: 中国
  • 抗原 See all COA5 蛋白
    COA5 (Cytochrome C Oxidase Assembly Factor 5 (COA5))
    蛋白类型
    Recombinant
    宿主
    • 1
    • 1
    • 1
    • 1
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    资源
    • 5
    • 2
    HEK-293 Cells
    标记
    This COA5 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Chromosome 2 open reading frame 64 (C2orf64) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product COA5 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    COA5 (Cytochrome C Oxidase Assembly Factor 5 (COA5))
    别名
    Chromosome 2 Open Reading Frame 64 (c2orf64) (COA5 产品)
    别名
    C2orf64 Protein, C11H2ORF64 Protein, 6330578E17Rik Protein, Pet191 Protein, 1700001A24Rik Protein, zgc:153408 Protein, c2orf64 Protein, pet191 Protein, chromosome 2 open reading frame 64 Protein, cytochrome c oxidase assembly factor 5 Protein, cytochrome C oxidase assembly factor 5 Protein, cytochrome c oxidase assembly factor 5 S homeolog Protein, COA5 Protein, Coa5 Protein, coa5 Protein, coa5.S Protein
    背景
    This gene encodes an ortholog of yeast Pet191, which in yeast is a subunit of a large oligomeric complex associated with the mitochondrial inner membrane, and required for the assembly of the cytochrome c oxidase complex. Mutations in this gene are associated with mitochondrial complex IV deficiency, a disorder of the mitochondrial respiratory chain with heterogeneous clinical manifestations, ranging from isolated myopathy to a severe disease affecting several tissues and organs.
    分子量
    8.2 kDa
    NCBI登录号
    NP_001008216
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