Tri-Methyl-Histone H3 (Lys36) (D5A7) XP   Rabbit mAb__®产品图

Tri-Methyl-Histone H3 (Lys36)

(D5A7) XP Rabbit mAb__®
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  • 询价
  • Cell Signaling Technology已认证
  • 4909
  • USA
  • 2026年05月28日
  • W, ChIP
  • H,M,R,Mk,Hm,C,Dm,X,Z,B
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Tri-Methyl-Histone H3 (Lys36) (D5A7) XP Rabbit mAb__®

    • 抗原

      synthetic peptide corresponding to the amino terminus of histone H3 in which Lys36 is tri-methylated

    • 应用范围

      W, ChIP

    • 保质期

      详见说明书

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 适应物种

      H,M,R,Mk,Hm,C,Dm,X,Z,B

    • 库存

      大量

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      40 ul (4 western blots)/100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:40 ul (4 western blots)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  ChIP=Chromatin IP
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Hm=Hamster  Mk=Monkey  C=Chicken  Dm=D. melanogaster  X=Xenopus  Z=Zebrafish  B=Bovine
    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 ChIP H M R Mk (Hm) (C) (Dm) (X) (Z) (B) Endogenous 17 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    Tri-Methyl-Histone H3 (Lys36) (D5A7) XP® Rabbit mAb detects endogenous levels of histone H3 only when tri-methylated on Lys36. The antibody does not cross-react with non-methylated, mono-methylated, or di-methylated Lys36. In addition, the antibody does not cross-react with histone H3 methylated at Lys4, Lys9, Lys27 or histone H4 methylated at Lys20.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to the amino terminus of histone H3 in which Lys36 is tri-methylated.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using Tri-Methyl-Histone H3 (Lys36) (D5A7) XP® Rabbit mAb.

    ELISA

    ELISA

    Tri-Methyl Histone H3 (Lys36) (D5A7) XP® Rabbit mAb specificity was determined by peptide ELISA. The graph depicts the binding of the antibody to pre-coated tri-methyl histone H3 (Lys36) peptide in the presence of increasing concentrations of various competitor peptides. As shown, only the tri-methyl histone H3 (Lys36) peptide competed away binding of the antibody.

    Chromatin IP

    Chromatin IP

    Chromatin immunoprecipitations were performed with cross-linked chromatin from 4 x 106 HeLa cells and either 10 μl of Tri-Methyl-Histone H3 (Lys36) (D5A7) XP® Rabbit mAb or 2 μl of Normal Rabbit IgG #2729 using SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003. The enriched DNA was quantified by real-time PCR using SimpleChIP® Human γ-Actin Promoter Primers #5037, SimpleChIP® Human γ-Actin Intron 3 Primers #5047, SimpleChIP® Human GAPDH Promoter Primers #4471, and SimpleChIP® Human GAPDH Intron 2 Primers #4478. The amount of immunoprecipitated DNA in each sample is represented as signal relative to the total amount of input chromatin, which is equivalent to one.


    Background

    The nucleosome, made up of four core histone proteins (H2A, H2B, H3, and H4), is the primary building block of chromatin. Originally thought to function as a static scaffold for DNA packaging, histones have now been shown to be dynamic proteins, undergoing multiple types of post-translational modifications, including acetylation, phosphorylation, methylation, and ubiquitination (1). Histone methylation is a major determinant for the formation of active and inactive regions of the genome and is crucial for the proper programming of the genome during development (2,3). Arginine methylation of histones H3 (Arg2, 17, 26) and H4 (Arg3) promotes transcriptional activation and is mediated by a family of protein arginine methyltransferases (PRMTs), including the co-activators PRMT1 and CARM1 (PRMT4) (4). In contrast, a more diverse set of histone lysine methyltransferases has been identified, all but one of which contain a conserved catalytic SET domain originally identified in the Drosophila Su(var)3-9, Enhancer of zeste, and Trithorax proteins. Lysine methylation occurs primarily on histones H3 (Lys4, 9, 27, 36, 79) and H4 (Lys20) and has been implicated in both transcriptional activation and silencing (4). Methylation of these lysine residues coordinates the recruitment of chromatin modifying enzymes containing methyl-lysine binding modules such as chromodomains (HP1, PRC1), PHD fingers (BPTF, ING2), tudor domains (53BP1), and WD-40 domains (WDR5) (5-8). The discovery of histone demethylases such as PADI4, LSD1, JMJD1, JMJD2, and JHDM1 has shown that methylation is a reversible epigenetic marker (9).

    1. Peterson, C.L. and Laniel, M.A. (2004) Curr. Biol. 14, R546-R551.
    2. Kubicek, S. et al. (2006) Ernst Schering Res. Found Workshop , 1-27.
    3. Lin, W. and Dent, S.Y. (2006) Curr. Opin. Genet. Dev. 16, 137-142.
    4. Lee, D.Y. et al. (2005) Endocr. Rev. 26, 147-170.
    5. Daniel, J.A. et al. (2005) Cell Cycle 4, 919-926.
    6. Shi, X. et al. (2006) Nature 442, 96-99.
    7. Wysocka, J. et al. (2006) Nature 442, 86-90.
    8. Wysocka, J. et al. (2005) Cell 121, 859-872.
    9. Trojer, P. and Reinberg, D. (2006) Cell 125, 213-217.
    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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