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COMP antibody

COMP Reactivity: Human, Mouse, Rat IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7257527
  • Target See all COMP Antibodies
    COMP (Cartilage Oligomeric Matrix Protein (COMP))
    Reactivity
    • 59
    • 34
    • 26
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 73
    • 8
    • 1
    • 1
    Rabbit
    Clonality
    • 75
    • 8
    Polyclonal
    Conjugate
    • 33
    • 12
    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This COMP antibody is un-conjugated
    Application
    • 75
    • 24
    • 24
    • 22
    • 13
    • 10
    • 9
    • 7
    • 6
    • 4
    • 4
    • 3
    • 1
    • 1
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human COMP (NP_000086.2).
    Isotype
    IgG
    Top Product
    Discover our top product COMP Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    COMP (Cartilage Oligomeric Matrix Protein (COMP))
    Alternative Name
    COMP (COMP Products)
    Background
    The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Contraction or expansion of a 5 aa aspartate repeat and other mutations can cause pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED).
    Gene ID
    1311
    UniProt
    P49747
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