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COL9A1 antibody

The Rabbit Polyclonal anti-COL9A1 antibody has been validated for WB and IHC. It is suitable to detect COL9A1 in samples from Human and Mouse.
Catalog No. ABIN7011211

Quick Overview for COL9A1 antibody (ABIN7011211)

Target

See all COL9A1 Antibodies
COL9A1 (Collagen, Type IX, alpha 1 (COL9A1))

Reactivity

  • 28
  • 6
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 26
  • 6
Rabbit

Clonality

  • 29
  • 3
Polyclonal

Conjugate

  • 20
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This COL9A1 antibody is un-conjugated

Application

  • 23
  • 13
  • 13
  • 4
  • 4
  • 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

    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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