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HSP40 Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年08月18日
  • W, IP, IF-IC, F
  • Rabbit
  • H,M,R,Mk
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      HSP40 Antibody

    • 抗原

      synthetic peptide corresponding to Glu300 of human HSP40/Hdj1

    • 应用范围

      W, IP, IF-IC, F

    • 宿主

      Rabbit

    • 适应物种

      H,M,R,Mk

    • 库存

      大量

    • 供应商

      CST

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 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  IP=Immunoprecipitation  IF-IC=Immunofluorescence (Immunocytochemistry)  F=Flow Cytometry
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey
    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 IP IF-IC F H M R Mk Endogenous 40 Rabbit
    Protocols
    Specificity / Sensitivity

    HSP40 Antibody detects endogenous levels of total HSP40 protein. This antibody does not cross-react with other HSPs.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to Glu300 of human HSP40/Hdj1. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa, C2C12 and C6 cells, using HSP40 Antibody.

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of HeLa cells, using HSP40 Antibody (blue) compared to a nonspecific negative control antibody (red).

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HeLa cells, untreated (left) or heat-treated (right), using HSP40 Antibody (green). Actin filaments have been labeled with Alexa Fluor® 555 phalloidin (red).


    Background

    HSP40 and HSP40-like proteins represent a large family of chaperone proteins that are homologous to E. coli DnaJ protein (1). These proteins are classified into three subtypes based on their structures. The common feature of the family is a conserved J domain, which is usually located at the amino terminus of proteins and responsible for their association with HSP70 (1,2). Human HSP40, also known as Hdj1, belongs to subtype II that contain a unique Gly/Phe-rich region (2). HSP40 family proteins bind unfolded proteins, prevent their aggregation, and then deliver them to HSP70 (2,3). Another major function of HSP40 is to stimulate ATPase activity of HSP70, which causes conformational change of the unfolded proteins (4,5). The HSP40-HSP70-unfolded protein complex further binds to co-chaperones Hip, Hop and HSP90 or components of the protein degradation machinery such as CHIP and BAG-1, which either leads to protein folding or degradation, respectively (6).

    1. Cheetham, M.E. and Caplan, A.J. (1998) Cell Stress Chaperones 3, 28-36.
    2. Fan, C.Y. et al. (2003) Cell Stress Chaperones 8, 309-316.
    3. Langer, T. et al. (1992) Nature 356, 683-689.
    4. Liberek, K. et al. (1991) Proc. Natl. Acad. Sci. USA 88, 2874-2878.
    5. Cyr, D.M. et al. (1992) J. Biol. Chem. 267, 20927-20931.
    6. Höhfeld, J. et al. (2001) EMBO Rep. 2, 885-890.
    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
    • Peptide substrate identification for yeast Hsp40 Ydj1 by screening the phage display library

      We have identified a peptide substrate for molecular chaperone Hsp40 Ydj1 by utilizing the combination of phage display library screening and isothemol titration calirimetry (ITC). The initial peptide substrate screening for Hsp40 Ydj

    • 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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