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C1QBP antibody

C1QBP Reactivity: Human WB, IP, IF, FACS, Func, IA Host: Mouse Monoclonal 74-5-2 unconjugated
Catalog No. ABIN2191879
  • Target See all C1QBP Antibodies
    C1QBP (Complement Component 1, Q Subcomponent Binding Protein (C1QBP))
    Reactivity
    • 60
    • 40
    • 25
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 72
    • 16
    • 1
    Mouse
    Clonality
    • 74
    • 15
    Monoclonal
    Conjugate
    • 44
    • 12
    • 12
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C1QBP antibody is un-conjugated
    Application
    • 75
    • 26
    • 19
    • 14
    • 14
    • 13
    • 13
    • 13
    • 12
    • 8
    • 7
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    Western Blotting (WB), Immunoprecipitation (IP), Immunofluorescence (IF), Flow Cytometry (FACS), Functional Studies (Func), Immunoassay (IA)
    Cross-Reactivity (Details)
    Cross reactivity: Rat : Yes
    Sterility
    0.2 μm filtered
    Clone
    74-5-2
    Isotype
    IgG1
    Top Product
    Discover our top product C1QBP Primary Antibody
  • Application Notes
    For flow cytometry and Western blotting, dilutions to be used depend on detection system applied. It is recommended that users test the reagent and determine their own optimal dilutions. The typical starting working dilution is 1:50. For functional studies, in vitro dilutions have to be optimized in user's experimental setting. Website:
    Restrictions
    For Research Use only
  • Buffer
    PBS, containing 0.1 % bovine serum albumin.
    Storage
    4 °C
    Storage Comment
    Product should be stored at 4 °C. Under recommended storage conditions, product is stable for one year.
    Expiry Date
    12 months
  • Sansonno, Tucci, Ghebrehiwet, Lauletta, Peerschke, Conteduca, Russi, Gatti, Sansonno, Dammacco: "Role of the receptor for the globular domain of C1q protein in the pathogenesis of hepatitis C virus-related cryoglobulin vascular damage." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 183, Issue 9, pp. 6013-20, (2009) (PubMed).

    Peerschke, Bayer, Ghebrehiwet, Xiong: "gC1qR/p33 blockade reduces Staphylococcus aureus colonization of target tissues in an animal model of infective endocarditis." in: Infection and immunity, Vol. 74, Issue 8, pp. 4418-23, (2006) (PubMed).

    Ghebrehiwet, Lim, Kumar, Feng, Peerschke: "gC1q-R/p33, a member of a new class of multifunctional and multicompartmental cellular proteins, is involved in inflammation and infection." in: Immunological reviews, Vol. 180, pp. 65-77, (2001) (PubMed).

    Ghebrehiwet, Lu, Zhang, Lim, Eggleton, Leigh, Reid, Peerschke: "Identification of functional domains on gC1Q-R, a cell surface protein that binds to the globular "heads" of C1Q, using monoclonal antibodies and synthetic peptides." in: Hybridoma, Vol. 15, Issue 5, pp. 333-42, (1997) (PubMed).

  • Target
    C1QBP (Complement Component 1, Q Subcomponent Binding Protein (C1QBP))
    Abstract
    C1QBP Products
    Synonyms
    SF2 antibody, X38k antibody, gC1qR antibody, C1QBP antibody, GC1QBP antibody, HABP1 antibody, SF2p32 antibody, gC1Q-R antibody, p32 antibody, AA407365 antibody, AA986492 antibody, D11Wsu182e antibody, P32 antibody, gC1qBP antibody, Habp1 antibody, complement C1q binding protein antibody, complement component 1, q subcomponent binding protein S homeolog antibody, complement component 1, q subcomponent binding protein antibody, C1QBP antibody, c1qbp.S antibody, LOC100227158 antibody, C1qbp antibody
    Background
    The monoclonal antibody 74.5.2 recognizes a cell membrane C1q binding molecule that recognises the globular heads of C1q. It is also present in plasma and the extracellular matrix. The molecule is an unusually acidic, single chain protein with an apparent molecular weight of 33 kDa. It does not possess a conventional sequence motif compatible with a membrane spanning segment nor a consensus site for a GPI anchor. gC1qR migrates as a single chain under both reducing and non-reducing conditions, but it behaves as an oligomer on gel-filtration in non-dissociating conditions. Its multimer formation may be a critical process by which the gC1qR molecule increases its affinity for multivalent ligands such as C1q. gC1qR has been shown to inhibit complement activation by preventing the binding of C1q to antibodies, suggesting that the binding site for gC1qR and the binding site for immune complexes, which are present on the C1q globular 'heads', may be located at the same position. gC1qR is capable of interacting with several proteins involved in blood clotting, namely, thrombin, prothrombin, the heparinbinding form of vitronectin, the ternary complex, vitronectin-thrombin-antithrombin, as well as high-molecular-weight kininogen and Hageman factor. Besides its role in the complement pathway, gC1qR participates in enhancement of Fc-receptor and CR1-mediated phagocytosis, procoagulant activity on platelets, and chemotactic activity on mast cells, eosinophils, neutrophils, and fibroblasts. gC1qR is expressed on a wide variety of cells and can serve as a binding site for plasma and microbial proteins. Its antigenic sites may be cryptic on cells in suspension but become exposed when the cells are fixed by bifunctional cross-linkers. Probably it is also expressed on the cell membrane as a tetramer. Crosslinking or activation may thus bring about a tetrameric assembly of gC1qR followed by a conformational change within the molecule, thereby exposing epitopes which are otherwise hidden. A form of gC1qR is also found inside the cell. Intracellular gC1qR has been shown to bind the cytoplasmic tail of the α1B-adrenergic receptor and to PKCμ. The monoclonal antibody 74.5.2 is directed against epitopes in the XC15 peptide that contains a binding site for high-molecular-weight kininogen and Factor XII.
    Pathways
    Ribonucleoprotein Complex Subunit Organization, Ribosome Assembly
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