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NDUFAF1 Protein (Myc-DYKDDDDK Tag)

NDUFAF1 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 ABIN2727012
发货至: 中国
  • 抗原 See all NDUFAF1 蛋白
    NDUFAF1 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 1 (NDUFAF1))
    蛋白类型
    Recombinant
    宿主
    • 2
    • 1
    • 1
    • 1
    • 1
    资源
    • 3
    • 2
    • 1
    HEK-293 Cells
    标记
    This NDUFAF1 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human NDUFAF1 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 NDUFAF1 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
    NDUFAF1 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 1 (NDUFAF1))
    别名
    Ndufaf1 (NDUFAF1 产品)
    别名
    2410001M24Rik Protein, CGI-65 Protein, CIA30 Protein, CGI65 Protein, Cia30 Protein, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 1 Protein, NADH:ubiquinone oxidoreductase complex assembly factor 1 Protein, Ndufaf1 Protein, NDUFAF1 Protein
    背景
    This gene encodes a complex I assembly factor protein. Complex I (NADH-ubiquinone oxidoreductase) 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. The encoded protein is required for assembly of complex I, and mutations in this gene are a cause of mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19.
    分子量
    37.6 kDa
    NCBI登录号
    NP_057097
    途径
    SARS-CoV-2 Protein Interactome
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