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SURF1 抗体

SURF1 适用: 人, 大鼠, 小鼠 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7256170
发货至: 中国
  • 抗原 See all SURF1 抗体
    SURF1 (Surfeit 1 (SURF1))
    适用
    • 22
    • 7
    • 7
    • 2
    • 2
    • 2
    • 1
    人, 大鼠, 小鼠
    宿主
    • 22
    • 1
    克隆类型
    • 23
    多克隆
    标记
    • 16
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SURF1 antibody is un-conjugated
    应用范围
    • 16
    • 7
    • 6
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human SURF1 (NP_003163.1).
    亚型
    IgG
    Top Product
    Discover our top product SURF1 Primary Antibody
  • 应用备注
    IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    SURF1 (Surfeit 1 (SURF1))
    别名
    SURF1 (SURF1 产品)
    别名
    BcDNA:GH23574 antibody, CG9943 antibody, Dmel\\CG9943 antibody, GB14201 antibody, SURF1 antibody, im:6898613 antibody, zgc:158646 antibody, Ab1-205 antibody, SURF-1 antibody, 0610010F23Rik antibody, Surf-1 antibody, SURFEIT 1 antibody, Surfeit 1 antibody, surfeit locus protein 1 antibody, SURF1, cytochrome c oxidase assembly factor antibody, surfeit 1 antibody, surfeit gene 1 antibody, Surfeit locus 1 cytochrome c oxidase biogenesis protein antibody, Surf1 antibody, LOC413781 antibody, SURF1 antibody, surf1 antibody
    背景
    This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency.
    基因ID
    6834
    UniProt
    Q15526
    途径
    Proton Transport, Ribonucleoside Biosynthetic Process
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