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p67phox Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月30日
  • W
  • Rabbit
  • H,M,R
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      p67phox Antibody

    • 抗原

      synthetic peptide corresponding to residues surrounding Ala25 of human p67phox

    • 应用范围

      W

    • 宿主

      Rabbit

    • 保质期

      详见说明书

    • 适应物种

      H,M,R

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 是否单克隆

      2

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting
    Reactivity Key:  H=Human  M=Mouse  R=Rat
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W H M R Endogenous 67 Rabbit
    Protocols
    Specificity / Sensitivity

    p67phox Antibody detects endogenous levels of total p67phox protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala25 of human p67phox. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from RAW 264.7 and C6 cells using p67phox Antibody.

    Background

    The phagocytic NADPH oxidase is a multiprotein enzyme that catalyzes the reduction of oxygen to superoxide in response to pathogenic invasion. The NADPH oxidase consists of 6 subunits, including the membrane-bound p91 phox and p22 phox heterodimers (also known as cytochrome b558), the cytosolic complex of p40phox, p47phox and p67phox, and the small GTPase Rac2. Activation of NADPH oxidase is initiated by cytosolic complex phosphorylation, which induces a conformational change that leads to the translocation of the cytosolic complex to the membrane and formation of an active enzyme with cytochrome b558 (1). Defects in p47phox, often resulting from recombination between p47phox and a nearby homologous pseudogene, cause chronic granulomatous disease (2-4). Elevated oxidative stress due to increased myocardial NADPH oxidase activity may be a contributing factor in heart failure (5,6).

    p67phox appears to coordinate assembly of NAPDH oxidase as it associates with multiple subunits as well as the α subunit of heterotrimeric G proteins (7). Mutations in the corresponding p67phox gene are also associated with a form of autosomal recessive chronic granulomatous disease (8).

    1. Babior, B.M. (1999) Blood 93, 1464-76.
    2. Noack, D. et al. (2001) Blood 97, 305-11.
    3. Görlach, A. et al. (1997) J Clin Invest 100, 1907-18.
    4. Chanock, S.J. et al. (2000) Blood Cells Mol Dis 26, 37-46.
    5. Heymes, C. et al. (2003) J Am Coll Cardiol 41, 2164-71.
    6. Doerries, C. et al. (2007) Circ Res 100, 894-903.
    7. Marty, C. et al. (2006) Mol Cell Biol 26, 5190-200.
    8. Leto, T.L. et al. (1990) Science 248, 727-30.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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    图标文献和实验
    相关实验
    • Translocation of p47phox and Activation of NADPH Oxidase in Mononuclear Cells

      subunits. Equimolar amounts of p47phox and p67phox in the cytosol combine to a form a highly basic 250 kDa protein. During activation, this complex migrates from the cytosol to the membrane where this complex combines with cytochrome b558 , which in turn

    • Generation of Antibody Molecules Through Antibody Engineering

      been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional

    • The Antibody Molecule

      The importance of antibody molecules was first recognized in the 1890s, when it was shown that immunity to tetanus and diphtheria was caused by antibodies against the bacterial exotoxins (1 ). Around the same time, it was shown that antisera

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