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AOC3 antibody

AOC3 Reactivity: Mouse IF, IHC (fro), IP, Func Host: Rat Monoclonal 01-07-88 unconjugated
Catalog No. ABIN1105387
  • Target See all AOC3 Antibodies
    AOC3 (Amine Oxidase, Copper Containing 3 (Vascular Adhesion Protein 1) (AOC3))
    Reactivity
    • 49
    • 4
    • 4
    Mouse
    Host
    • 36
    • 10
    • 3
    • 1
    Rat
    Clonality
    • 38
    • 11
    • 1
    Monoclonal
    Conjugate
    • 27
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This AOC3 antibody is un-conjugated
    Application
    • 37
    • 24
    • 13
    • 13
    • 9
    • 9
    • 8
    • 6
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    Immunofluorescence (IF), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunoprecipitation (IP), Functional Studies (Func)
    Specificity
    The monoclonal antibody 7-88 recognizes mouse Vascular Adhesion Protein-1 (VAP-1) which is a glycosylated homodimeric membrane protein consisting of two 90 kDa subunits connected by disulfide bonds. It inhibits migration of granulocytes and monocytes in acute models of inflammation.
    Cross-Reactivity (Details)
    Species reactivity (tested):Mouse.
    Purification
    Protein G Chromatography
    Immunogen
    Vessels from mouse lymph nodes
    Clone
    01-07-88
    Isotype
    IgG2b
    Top Product
    Discover our top product AOC3 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Concentration
    0.1 mg/mL
    Buffer
    PBS, 0.1 % BSA
    Storage
    4 °C
    Storage Comment
    Store undiluted at 2-8 °C.
  • Target
    AOC3 (Amine Oxidase, Copper Containing 3 (Vascular Adhesion Protein 1) (AOC3))
    Alternative Name
    AOC3 / VAP1 (AOC3 Products)
    Background
    VAP-1 is a glycosylated homodimeric membrane protein consisting of two 90 kDa subunits connected by disulfide bonds. It contains a short N-terminal cytoplasmic tail, a single membrane-spanning domain and a large extracellular part. A soluble form of VAP-1 (sVAP-1) has been described, which presumably results from the proteolytic cleavage of membrane-bound VAP-1. Structurally VAP-1 belongs to enzymes called semicarbamizide-sensitive amine oxidases, which contain copper as a cofactor. These enzymes deaminate primary amines in a reaction producing hydrogen peroxide, aldehyde, and ammonia. VAP-1 is expressed in endothelial cells, smooth muscle cells, adipocytes, and in follicular dendritic cells. In endothelial cells the majority of VAP-1 is stored within intracellular granules and translocated to the surface upon inflammation where it regulates leukocyte tissue infiltration. Furthermore, the end-products formed by VAP-1 can also regulate leukocyte migration by signaling effects, have insulin-like effects in energy metabolism, and can cause vascular damage by direct cytotoxicity. In white adipose tissue of obese and diabetic db-/- mice increased expression of VAP-1 has been observed suggesting that it contributes to the arthrosclerosis and vascular dysfunction observed in these diseases. Moreover, inhibition of VAP-1reduced the accumulation of myeloid cells into tumors and attenuates tumor growth.Synonyms: Copper amine oxidase, HPAO, Membrane primary amine oxidase, Semicarbazide-sensitive amine oxidase, Vascular adhesion protein 1
    Gene ID
    11754
    NCBI Accession
    NP_033805
    UniProt
    O70423
    Pathways
    Feeding Behaviour
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