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SURF1 抗体

This 兔 多克隆 antibody specifically detects SURF1 in WB. It exhibits reactivity toward 人.
产品编号 ABIN7469040
发货至: 中国
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Quick Overview for SURF1 抗体 (ABIN7469040)

抗原

See all SURF1 抗体
SURF1 (Surfeit 1 (SURF1))

适用

  • 22
  • 9
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宿主

  • 23
  • 1

克隆类型

  • 24
多克隆

标记

  • 17
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SURF1 antibody is un-conjugated

应用范围

  • 17
  • 8
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Western Blotting (WB)
  • 交叉反应

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human SURF1. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: Jurkat

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.83 mg/mL

    缓冲液

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    4 °C,-20 °C

    储存方法

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    SURF1 (Surfeit 1 (SURF1))

    别名

    SURF1 cytochrome c oxidase assembly factor

    背景

    Synonyms: SURF1 cytochrome c oxidase assembly factor , CMT4K

    Background: 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. [provided by RefSeq]

    分子量

    33 kDa

    基因ID

    6834

    UniProt

    Q15526

    途径

    Proton Transport, Ribonucleoside Biosynthetic Process
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