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HP1α/� (C7F11) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • 2623
  • USA
  • 2025年10月07日
  • W, IP, IHC-P, IF-IC
  • 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

      HP1α/� (C7F11) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to the carboxy terminus of human HP1 α

    • 应用范围

      W, IP, IHC-P, IF-IC

    • 适应物种

      H,M,R,Mk

    • 库存

      大量

    • 级别

      详见MSDS文件

    • 保质期

      详见说明书

    • 供应商

      CST

    • 是否单克隆

      1

    • 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  IHC-P=Immunohistochemistry (Paraffin)  IF-IC=Immunofluorescence (Immunocytochemistry)
    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) Isotype
    W IP IHC-P IF-IC H M R Mk Endogenous 25 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    HP1 α (C7F11) Rabbit mAb detects endogenous levels of total HP1 α protein. The antibody does not cross-react with HP1 β or HP1 γ proteins.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to the carboxy terminus of human HP1 α.

    Western Blotting

    Western Blotting

    Western blot analysis of lysates from HeLa, NIH/3T3, C6 and COS cells using HP1 α (C7F11) Rabbit mAb.

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human lung carcinoma, showing nuclear localization using HP1 α (C7F11) Rabbit mAb.

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human breast carcinoma using HP1 α (C7F11) Rabbit mAb in the presence of control peptide (left) or HP1 alpha blocking peptide #1004 (right).


    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HeLa cells using HP1α (C7F11) Rabbit mAb (green). Actin filaments have been labeled with Alexa Fluor® 555 phalloidin (red).

    Background

    Heterochromatin protein 1 (HP1) is a family of heterochromatic adaptor molecules involved in both gene silencing and higher order chromatin structure (1). All three HP1 family members (α, β, and γ) are primarily associated with centromeric heterochromatin; however, HP1β and γ also localize to euchromatic sites in the genome (2,3). HP1 proteins are approximately 25 kDa in size and contain a conserved amino-terminal chromodomain, followed by a variable hinge region and a conserved carboxy-terminal chromoshadow domain. The chromodomain facilitates binding to histone H3 tri-methylated at Lys9, a histone "mark" closely associated with centromeric heterochromatin (4,5). The variable hinge region binds both RNA and DNA in a sequence-independent manner (6). The chromoshadow domain mediates the dimerization of HP1 proteins, in addition to binding multiple proteins implicated in gene silencing and heterochromatin formation, including the SUV39H histone methyltransferase, the DNMT1 and DNMT3a DNA methyltransferases, and the p150 subunit of chromatin-assembly factor-1 (CAF1) (7-9). In addition to contributing to heterochromatin formation and propagation, HP1 and SUV39H are also found complexed with retinoblastoma (Rb) and E2F6 proteins, both of which function to repress euchromatic gene transcription in quiescent cells (10,11). HP1 proteins are subject to multiple types of post-translational modifications, including phosphorylation, acetylation, methylation, ubiquitination, and sumoylation, suggesting multiple means of regulation (12-14).

    1. Maison, C. and Almouzni, G. (2004) Nat. Rev. Mol. Cell Biol. 5, 296-304.
    2. Minc, E. et al. (2000) Cytogenet. Cell Genet. 90, 279-284.
    3. Nielsen, A.L. et al. (2001) Mol. Cell 7, 729-739.
    4. Lachner, M. et al. (2001) Nature 410, 116-120.
    5. Bannister, A.J. et al. (2001) Nature 410, 120-124.
    6. Muchardt, C. et al. (2002) EMBO Rep. 3, 975-981.
    7. Yamamoto, K. and Sonoda, M. (2003) Biochem. Biophys. Res. Commun. 301, 287-292.
    8. Fuks, F. et al. (2003) Nucleic Acids Res. 31, 2305-2312.
    9. Murzina, N. et al. (1999) Mol. Cell 4, 529-540.
    10. Nielsen, S.J. et al. (2001) Nature 412, 561-565.
    11. Ogawa, H. et al. (2002) Science 296, 1132-1136.
    12. Minc, E. et al. (1999) Chromosoma 108, 220-234.
    13. Zhao, T. et al. (2001) J. Biol. Chem. 276, 9512-9518.
    14. Lomberk, G. et al. (2006) Nat. Cell Biol. 8, 407-415.
    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
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    • Purification of mAb (IgG)

        Purification of mAb (IgG) by Chang-Duk Jun, 03/14/2000 Purpose Materials Antibody 7E3 , 2L sup grown in flasks, frozen and thawed overnight. BioRad Affi-Gel Protein A MAPS II Buffers

    • Testing Rabbit Bleeds By Elisa

      as a solid if soluble. Mix, adding glutaraldehyde last. Peptide and BSA turn a little yellow even before adding glutaraldehyde. Incubate 90'' at 37 deg C. Add 0.1 volumes of 0.1 M NaBH4 in 0.1 M NaHCO3. There will be some bubbling. Add

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