• merck millipore,默克密理博,04-825,Anti-PDGFRβ Antibody, clone 4A56, rabbit monoclonal
  • merck millipore,默克密理博,04-825,Anti-PDGFRβ Antibody, clone 4A56, rabbit monoclonal

    产品名称:Anti-PDGFRβ Antibody, clone 4A56, rabbit monoclonal
    产品型号:04-825
    This Anti-PDGFRβ Antibody, clone 4A56 is validated for use in IP, WB for the detection of PDGFRβ.

    merck millipore,默克密理博,04-825,Anti-PDGFRβ Antibody, clone 4A56, rabbit monoclonal

  • 产品介绍
  • merck millipore,默克密理博,04-825,Anti-PDGFRβ Antibody, clone 4A56, rabbit monoclonal

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    H, MWBRbCulture SupernatantMonoclonal Antibody
    描述
    产品目录编号 04-825
    Replaces 05-825
    品牌系列 Upstate
    商名
    • Upstate
    描述 Anti-PDGFRβ Antibody, clone 4A56, rabbit monoclonal
    产品信息
    格式 Culture Supernatant
    控制
    • RIPA lysates from mouse NIH/3T3, 3T3/A31, or human HFF cells
    演示 Cultured supernantant in 0.05% sodium azide
    应用
    应用 This Anti-PDGFRβ Antibody, clone 4A56 is validated for use in IP, WB for the detection of PDGFRβ.
    主要应用
    • Western Blotting
    应用说明 Westerm Blot Analysis:
    A 1:2,000 dilution of this lot detected PDGFRβ in RIPA lysates from mouse NIH/3T3, 3T3/A31, and human HFF cells.

    Immunoprecipitation: 4 μg of a previous lot immunoprecipitated PDGFRβ from 500 μg of 3T3/A31 RIPA lysate.
    生物信息
    免疫原品种 KLH-conjugated, synthetic peptide corresponding to amino acids 710-718 of human PDGF Receptor β. An N-terminus cysteine was added to facilitate conjugation. This sequence corresponds to amino acids 709-717 of mouse PDGF Receptor β.
    克隆 4A56
    宿主 Rabbit
    特异性 PDGFRβ, does not cross-react with EGF receptor
    同种型 IgG
    品种反应性 HumanMouse
    Species Reactivity Note Mouse and human.
    抗体类型 Monoclonal Antibody
    Entrez基因编号
    • NM_002608
    Entrez基因汇总 This gene encodes a cell surface tyrosine kinase receptor for members of the platelet-derived growth factor family. These growth factors are mitogens for cells of mesenchymal origin. The identity of the growth factor bound to a receptor monomer determines whether the functional receptor is a homodimer or a heterodimer, composed of both platelet-derived growth factor receptor alpha and beta polypeptides. This gene is flanked on chromosome 5 by the genes for granulocyte-macrophage colony-stimulating factor and macrophage-colony stimulating factor receptor; all three genes may be implicated in the 5-q syndrome. A translocation between chromosomes 5 and 12, that fuses this gene to that of the translocation, ETV6, leukemia gene, results in chronic myeloproliferative disorder with eosinophilia.
    基因符号
    • PDGFRB
    • PDGF-R-beta
    • CD140B
    • JTK12
    • PDGFR
    • CD140b
    • PDGFR1
    UniProt编号
    • P09619
    UniProt汇总 FUNCTION: SwissProt: P09619 # Receptor that binds specifically to PDGFB and PDGFD and has a tyrosine-protein kinase activity. Phosphorylates Tyr residues at the C-terminus of PTPN11 creating a binding site for the SH2 domain of GRB2.
    SIZE: 1106 amino acids; 123968 Da
    SUBUNIT: Homodimer, and heterodimer with PDGFRA. Interacts with APS. The autophosphorylated form interacts directly with SHB and with PIK3C2B, maybe indirectly.
    SUBCELLULAR LOCATION: Membrane; Single-pass type I membrane protein.
    DISEASE: SwissProt: P09619 # A chromosomal aberration involving PDGFRB is found in a form of chronic myelomonocytic leukemia (CMML). Translocation t(5;12)(q33;p13) with EVT6/TEL. It is characterized by abnormal clonal myeloid proliferation and by progression to acute myelogenous leukemia (AML). & A chromosomal aberration involving PDGFRB may be a cause of acute myelogenous leukemia. Translocation t(5;14)(q33;q32) with TRIP11. The fusion protein may be involved in clonal evolution of leukemia and eosinophilia. & A chromosomal aberration involving PDGFRB may be a cause of juvenile myelomonocytic leukemia. Translocation t(5;17)(q33;p11.2) with SPECC1. & A chromosomal aberration involving PDGFRB is a cause in many instances of chronic myeloproliferative disorder with eosinophilia (MPE) [MIM:131440]. Translocation t(5;12) with ETV6 on chromosome 12 creating an PDGFRB-ETV6 fusion protein. & A chromosomal aberration involving PDGFRB may be the cause of a myeloproliferative disorder (MBD) associated with eosinophilia. Translocation t(1;5)(q23;q33) that forms a PDE4DIP- PDGFRB fusion protein.
    SIMILARITY: SwissProt: P09619 ## Belongs to the protein kinase superfamily. Tyr protein kinase family. CSF-1/PDGF receptor subfamily. & Contains 5 Ig-like C2-type (immunoglobulin-like) domains. & Contains 1 protein kinase domain.
    产品使用声明
    质量保证 routinely evaluated by immunoblot on RIPA lysates from mouse NIH/3T3, 3T3/A31, or human HFF cells
    使用声明
    • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
    储存和货运信息
    存储条件 Stable for 1 year at -20°C from date of receipt.
    For maximum recovery of product, centrifuge the vial prior to removing the cap.
    包装信息
    数量 100 µL

    merck millipore,默克密理博,04-825,Anti-PDGFRβ Antibody, clone 4A56, rabbit monoclonal

上一件merck millipore产品:merck millipore,默克密理博,01-201,Heregulin-β3, Epidermal growth factor (EGF) domain
下一件merck millipore产品:merck millipore,默克密理博,05-1238,Anti-PARN Antibody, clone 7A7.1



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