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SH3BP2 Antibody, Biotin conjugated

  • 中文名稱:
    SH3BP2兔多克隆抗體, Biotin偶聯
  • 貨號:
    CSB-PA021224LD01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) SH3BP2 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
  • 別名:
    3BP-2 antibody; 3BP2 antibody; 3BP2_HUMAN antibody; Abl SH3 binding protein 2 antibody; Cherubism antibody; CRBM antibody; CRPM antibody; FLJ42079 antibody; FLJ54978 antibody; RES4-23 antibody; SH3 domain binding protein 2 antibody; SH3 domain-binding protein 2 antibody; Sh3bp2 antibody; TNFAIP3 interacting protein 2 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human SH3 domain-binding protein 2 protein (165-301AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Biotin
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA
  • Protocols:
  • 儲存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期:
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
  • 用途:
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 功能:
    Binds differentially to the SH3 domains of certain proteins of signal transduction pathways. Binds to phosphatidylinositols; linking the hemopoietic tyrosine kinase fes to the cytoplasmic membrane in a phosphorylation dependent mechanism.
  • 基因功能參考文獻:
    1. All members featured a heterozygous missense c.1244G>C; p.Arg415Pro SH3BP2 mutation PMID: 28721660
    2. The adaptor 3BP2 is required for KIT receptor expression and human mast cell survival. PMID: 25810396
    3. A c.1244G>A (p.Arg415Gln) mutation in SH3BP2 gene causes cherubism in a Turkish family PMID: 24608212
    4. Authors conclude that a novel p.Asp419Tyr alteration in SH3BP2 to be a cherubism-causing mutation in a Turkish family. PMID: 23083484
    5. In the first family, a missense mutation Arg415Gln was found in exon 9 of SH3BP2 in all affected individuals. The unaffected individuals did not have the mutation. In the second family, a missense mutation Pro418Thr was identified in exon 9 of the SH3BP2 PMID: 22795151
    6. These results demonstrate that PARP1 regulates expression of SH3BP2. PMID: 22820184
    7. P416R mutation of 3BP2 causes the gain of function in B cells by increasing the interaction with specific signaling molecules. PMID: 21794028
    8. if a primary genetic defect is the cause for CGCG it is either located in SH3BP2 gene exons not yet related to cherubism or in a different gene. PMID: 21680150
    9. The SH-3BP-2 mutation may participate in the differentiation and maturation of osteoclast-like cells in the lesion of cherubism. PMID: 19576004
    10. over expression of SH3BP2 in RAW 264.7 cells potentiates sRANKL-stimulated phosphorylation of PLCgamma1 and PLCgamma2. PMID: 20872577
    11. No SH3BP2 gene mutation was found in PGCL. PMID: 20002873
    12. Regulation of FcepsilonRI-mediated degranulation by an adaptor protein 3BP2 in rat basophilic leukemia RBL-2H3 cells. PMID: 12200378
    13. 3BP2 may regulate b cell receptor-mediated gene activation through Vav proteins. PMID: 15345594
    14. Adaptor protein SH3BP2 regulates transcription factors through its tyrosine phosphorylation and SH2 domain. PMID: 15751964
    15. CD244-3BP2 association regulates cytolytic function but not IFN-gamma release PMID: 16177062
    16. no mutations...in giant cell granuloma PMID: 16713042
    17. How SH3BP2 affects leukocyte signaling and influences cherubism PMID: 16802602
    18. a novel A1517G missense mutation at the SH3BP2 gene in a Chinese family with multiple affected individuals with cherubism was identified PMID: 17147794
    19. Mutated in a rare human disease involved in cranial-facial development called cherubism, suggesting a role for 3BP2 in regulating osteoclast and hematopoietic cell function. [REVIEW] PMID: 17156730
    20. unexpected role of 3BP2 in endocytic and cytoskeletal regulation through its interaction with CIN85 and HIP-55 PMID: 17306257
    21. A new mutation in a family affected with cherubism PMID: 17321449
    22. People with Giant Cell Granuloma of the Jaw do not harbour cherubism-related germline SH3BP2 mutations. PMID: 17544554
    23. Point mutations in the SH3BP2 gene have been revealed in cherubism patients. PMID: 18596838
    24. 2 novel mutations were found; heterozygous missense mutation c.1442A>T (Q481L) in exon 11 in one sporadic case of CGCL and heterozygous germline and tumor tissue missense mutation c.320C>T (T107M) in exon 4 in one patient with cherubism. PMID: 19017279
    25. 3BP2 induces the protein complex with cellular signaling molecules through phosphorylation of Tyr(183) and SH2 domain leading to the activation of NFAT in B cells PMID: 19833725

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  • 相關疾病:
    Cherubism (CRBM)
  • 組織特異性:
    Expressed in a variety of tissues including lung, liver, skeletal muscle, kidney and pancreas.
  • 數據庫鏈接:

    HGNC: 10825

    OMIM: 118400

    KEGG: hsa:6452

    STRING: 9606.ENSP00000422168

    UniGene: Hs.167679



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