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CCM2 antibody

CCM2 Reactivity: Human WB, IF Host: Mouse Monoclonal 5H4 unconjugated
Catalog No. ABIN2725247
  • Target See all CCM2 Antibodies
    CCM2 (Cerebral Cavernous Malformation 2 (CCM2))
    Reactivity
    • 24
    • 5
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 19
    • 4
    • 1
    Mouse
    Clonality
    • 23
    • 1
    Monoclonal
    Conjugate
    • 17
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CCM2 antibody is un-conjugated
    Application
    • 14
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Characteristics
    Homo sapiens cerebral cavernous malformation 2 (CCM2), transcript variant 2
    Purification
    Purified from mouse ascites fluids by affinity chromatography
    Immunogen
    Full length human recombinant protein of human CCM2(NP_113631) produced in HEK293T cell.
    Clone
    5H4
    Isotype
    IgG2b
    Top Product
    Discover our top product CCM2 Primary Antibody
  • Application Notes
    WB 1:2000, IF 1:100,
    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5-1.0 mg/mL
    Buffer
    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
  • Target
    CCM2 (Cerebral Cavernous Malformation 2 (CCM2))
    Alternative Name
    CCM2 (CCM2 Products)
    Synonyms
    C7orf22 antibody, OSM antibody, malcavernin antibody, CCM2 antibody, BC029157 antibody, TUF2 antibody, vtn antibody, zgc:110233 antibody, CCM2 scaffolding protein antibody, cerebral cavernous malformation 2 antibody, malcavernin antibody, CCM2 antibody, Ccm2 antibody, LOC100304744 antibody, ccm2 antibody
    Background
    This gene encodes a scaffold protein that functions in the stress-activated p38 Mitogen-activated protein kinase (MAPK) signaling cascade. The protein interacts with SMAD specific E3 ubiquitin protein ligase 1 (also known as SMURF1) via a phosphotyrosine binding domain to promote RhoA degradation. The protein is required for normal cytoskeletal structure, cell-cell interactions, and lumen formation in endothelial cells. Mutations in this gene result in cerebral cavernous malformations. Multiple transcript variants encoding different isoforms have been found for this gene.
    Molecular Weight
    48.7 kDa
    Gene ID
    83605
    NCBI Accession
    NM_031443
    HGNC
    83605
    Pathways
    Cell-Cell Junction Organization
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