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COL9A1 antibody

COL9A1 Reactivity: Human, Mouse WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7011211
  • Target See all COL9A1 Antibodies
    COL9A1 (Collagen, Type IX, alpha 1 (COL9A1))
    Reactivity
    • 28
    • 5
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 25
    • 5
    Rabbit
    Clonality
    • 28
    • 2
    Polyclonal
    Conjugate
    • 18
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This COL9A1 antibody is un-conjugated
    Application
    • 21
    • 13
    • 11
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human COL9A1 (NP_001842.3).
    Isotype
    IgG
  • Application Notes
    WB 1:500-1:2000 IHC 1:50-1:100
    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
    COL9A1 (Collagen, Type IX, alpha 1 (COL9A1))
    Alternative Name
    COL9A1 (COL9A1 Products)
    Background
    This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20 % ) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene.
    Molecular Weight

    Observed_MW: 65 kDa

    Calculated_MW: 35 kDa/64 kDa/91 kDa

    Gene ID
    1297
    UniProt
    P20849
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