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MeCP2 (D4F3) XP Rabbit mAb__

®
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  • 询价
  • Cell Signaling Technology已认证
  • 3456
  • USA
  • 2025年08月20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

      MeCP2 (D4F3) XP Rabbit mAb__®

    • 抗原

      synthetic peptide corresponding to the carboxy terminus of human MeCP2

    • 应用范围

      W, IP, IHC-P, IF-IC

    • 适应物种

      H,M,R,Mk

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 供应商

      CST

    • 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  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 75 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    MeCP2 (D4F3) XP® Rabbit mAb detects endogenous levels of MeCP2 (both isoforms A and B). This antibody does not cross-react with other MBD proteins.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to the carboxy terminus of human MeCP2.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using MeCP2 (D4F3) XP® Rabbit mAb.

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded human lung carcinoma using MeCP2 (D4F3) XP® Rabbit mAb.

    IHC-P (paraffin)

    IHC-P (paraffin)

    Immunohistochemical analysis of paraffin-embedded mouse brain using MeCP2 (D4F3) XP® Rabbit mAb in the presence of control peptide (left) and antigen-specific peptide (right).


    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of SH-SY5Y cells using MeCP2 (D4F3) XP® Rabbit mAb (green). Actin filaments have been labeled with DY-554 phalloidin (red).

    Background

    Methyl-CpG-binding protein 2 (MeCP2) is the founding member of a family of methyl-CpG-binding domain (MBD) proteins that also includes MBD1, MBD2, MBD3, MBD4, MBD5 and MBD6 (1-3). Apart from MBD3, these proteins bind methylated cytosine residues in the context of the di-nucleotide 5�-CG-3� to establish and maintain regions of transcriptionally inactive chromatin by recruiting a variety of co-repressor proteins (2). MeCP2 recruits histone deacetylases HDAC1 and HDAC2, and the DNA methyltransferase DNMT1 (4-6). MBD1 couples transcriptional silencing to DNA replication and interacts with the histone methyltransferases ESET and SUV39H1 (7,8). MBD2 and MBD3 co-purify as part of the NuRD (nucleosome remodeling and histone de-acetylation) co-repressor complex, which contains the chromatin remodeling ATPase Mi-2, HDAC1 and HDAC2 (9,10). MBD5 and MBD6 have recently been identified and little is known regarding their protein interactions. MBD proteins are associated with cancer and other diseases; MBD4 is best characterized for its role in DNA repair and MBD2 has been linked to intestinal cancer (11,12). Mutations in the MeCP2 gene cause the neurologic developmental disorder Rett Syndrome (13). MeCP2 protein levels are high in neurons, where it plays a critical role in multiple synaptic processes (14). In response to various physiological stimuli, MeCP2 is phosphorylated on Ser421 and regulates the expression of genes controlling dendritic patterning and spine morphogenesis (14). Disruption of this process in individuals with altered MeCP2 may cause the pathological changes seen in Rett Syndrome.

    1. Clouaire, T. and Stancheva, I. (2008) Cell Mol Life Sci 65, 1509-22.
    2. Hendrich, B. and Bird, A. (1998) Mol Cell Biol 18, 6538-47.
    3. Roloff, T.C. et al. (2003) BMC Genomics 4, 1.
    4. Nan, X. et al. (1998) Nature 393, 386-9.
    5. Jones, P.L. et al. (1998) Nat Genet 19, 187-91.
    6. Fuks, F. et al. (2003) J Biol Chem 278, 4035-40.
    7. Sarraf, S.A. and Stancheva, I. (2004) Mol Cell 15, 595-605.
    8. Fujita, N. et al. (2003) J Biol Chem 278, 24132-8.
    9. Zhang, Y. et al. (1999) Genes Dev 13, 1924-35.
    10. Wade, P.A. et al. (1999) Nat Genet 23, 62-6.
    11. Hendrich, B. et al. (1999) Nature 401, 301-4.
    12. Sansom, O.J. et al. (2003) Nat Genet 34, 145-7.
    13. Miltenberger-Miltenyi, G. and Laccone, F. (2003) Hum Mutat 22, 107-15.
    14. Zhou, Z. et al. (2006) Neuron 52, 255-69.
    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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    • 三生三世,一场组化,一次豪赌

      h)即可。2. 修复大法——不仅仅是「煮一煮」微波炉修复:简单易行效果好,CST 推荐使用微波炉完成修复。合适的修复液:根据抗体说明书使用合适的修复液。用柠檬酸修复后,切片需浸泡在修复液中,自然冷却;而用 EDTA 修复后,切片可直接从修复缸中取出,直接进行下一步。注:使用不同的修复方式和不同生产商的抗体检测人肺癌组织中 EGFR 的表达。第一排为 CST 的 EGF Receptor (D38B1) XP® Rabbit mAb(#4267),EDTA 的修复方式明显优于柠檬酸盐及胃蛋白

    • Using Soil DNA Kit (D5625) to Clean Up DNA containing inhibitors

      ) and incubate for 4 minutes. Centrifuge at max speed for 30 seconds and discard flowthrough. 7. Add equal volume of XP2 buffer to the cleared lysate, mix the sample throughly by vortexing. 8. Apply entire sample including any precipitation

    • 手把手课程之 IHC 关键操作步骤

      的染色强度。获得合适的染色强度后,将载玻片置于蒸馏水 (dH2O) 中以阻止进一步显色。抗体:Phospho–Stat3(Tyr705)(D3A7) XP® Rabbit mAb #9145样本:石蜡包埋的人类乳腺肿瘤显色检测:利用 SignalStain® DAB Substrate Kit #8059(左),竞争者提供的 DAB(中和右)CST 的 IHC/IF 明星产品推荐:生化试剂:Catalog NumberProduct NameProduct

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