Anti-Jarid2抗体- ChIP Grade (ab93288)


  • 产品名称Anti-Jarid2抗体- ChIP Grade
    参阅全部 Jarid2 一抗
  • 描述
    小鼠多克隆抗体to Jarid2 - ChIP Grade
  • 经测试应用适用于: WB, ELISA, ChIPmore details
  • 种属反应性
    与反应: Human
  • 免疫原

    Partial recombinant fragment corresponding to amino acids 1130-1230 (LQLETSERRC QICQHLCYLS MVVQENENVV FCLECALRHV EKQKSCRGLK LMYRYDEEQI ISLVNQICGK VSGKNGSIEN CLSKPTPKRG PRKRATVDVP) of Human Jarid2 (NP_004964) with a proprietary tag.

  • 阳性对照
    • 293 cell lysate



Our Abpromise guarantee covers the use of ab93288 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

应用 Ab评论 说明
WB 1/500 - 1/2500. Predicted molecular weight: 139 kDa.
ELISA Use at an assay dependent dilution.
ChIP Use at an assay dependent concentration.


  • 功能Regulator of histone methyltransferase complexes that plays an essential role in embryonic development, including heart and liver development, neural tube fusion process and hematopoiesis. Acts by modulating histone methyltransferase activity and promoting the recruitment of histone methyltransferase complexes to their target genes. Binds DNA and mediates the recruitment of the PRC2 complex to target genes in embryonic stem cells. Does not have histone demethylase activity but regulates activity of various histone methyltransferase complexes. In embryonic stem cells, it associates with the PRC2 complex and inhibits trimethylation of 'Lys-27' of histone H3 (H3K27me3) by the PRC2 complex, thereby playing a key role in differentiation of embryonic stem cells and normal development. In cardiac cells, it is required to repress expression of cyclin-D1 (CCND1) by activating methylation of 'Lys-9' of histone H3 (H3K9me) by the GLP1/EHMT1 and G9a/EHMT2 histone methyltransferases. Also acts as a transcriptional repressor of ANF via its interaction with GATA4 and NKX2-5. Participates in the negative regulation of cell proliferation signaling.
  • 组织特异性During embryogenesis, predominantly expressed in neurons and particularly in dorsal root ganglion cells.
  • 序列相似性Contains 1 ARID domain.
    Contains 1 JmjC domain.
    Contains 1 JmjN domain.
  • 结构域The ARID domain is required to target the PRC2 complex to its target genes.
    The GSGFP motif is required for the interaction with SUZ12.
  • 细胞定位Nucleus. Colocalizes with the PRC2 complex on chromatin.
  • Information by UniProt
  • 数据库链接
  • 别名
    • JARD2 antibody
    • JARD2_HUMAN antibody
    • JARID2 antibody
    • JMJ antibody
    • Jumonji AT rich interactive domain 2 antibody
    • Jumonji homolog antibody
    • Jumonji like protein antibody
    • Jumonji protein antibody
    • Jumonji/ARID domain containing protein 2 antibody
    • Jumonji/ARID domain-containing protein 2 antibody
    • Protein Jumonji antibody
    see all

Anti-Jarid2 antibody - ChIP Grade 图像

  • Anti-Jarid2 antibody - ChIP Grade (ab93288) at 5 µg/ml (in 5% non-fat milk/PBST (0.2%) blocking buffer) + 293 cell lysate at 50 µg

    Goat Anti-Mouse IgG (H&L)-HRP Conjugate at 1/1000 dilution
    Developed using the ECL technique

    Predicted band size : 139 kDa
  • Anti-Jarid2 antibody - ChIP Grade (ab93288) at 5 µg/ml (in 5% non-fat milk/PBST (0.2%) blocking buffer) + immunogen at 0.2 µg

    Goat Anti-Mouse IgG (H&L)-HRP Conjugate at 1/2500 dilution
    Developed using the ECL technique

    Predicted band size : 139 kDa
    Observed band size : 37.11 kDa (why is the actual band size different from the predicted?)

Anti-Jarid2 antibody - ChIP Grade (ab93288)参考文献

ab93288 has not yet been referenced specifically in any publications.

Product Wall

Abcam guarantees this product to work in the species/application used in this Abreview.
Application ChIP
Sample Human Cell lysate - nuclear (HeLa)
Specification HeLa
Type Cross-linking (X-ChIP)
Duration of cross-linking step: 10 minute(s) and 0 second(s)
Specification of the cross-linking agent: Formaldehyde
Detection step Real-time PCR
Positive control Total Input DNA
Negative control Nonspecific IgG immunoprecipitation

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提交于 Nov 23 2011