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COL2A1 antibody

The Mouse Monoclonal anti-COL2A1 antibody has been validated for IHC. It is suitable to detect COL2A1 in samples from Mouse and Rat.
Catalog No. ABIN7249870

Quick Overview for COL2A1 antibody (ABIN7249870)

Target

See all COL2A1 Antibodies
COL2A1 (Collagen, Type II, alpha 1 (COL2A1))

Reactivity

  • 91
  • 41
  • 39
  • 22
  • 12
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Mouse, Rat

Host

  • 86
  • 21
  • 3
  • 2
  • 1
Mouse

Clonality

  • 91
  • 22
Monoclonal

Conjugate

  • 68
  • 7
  • 6
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This COL2A1 antibody is un-conjugated

Application

  • 79
  • 46
  • 45
  • 26
  • 22
  • 13
  • 13
  • 12
  • 12
  • 12
  • 9
  • 5
  • 4
  • 4
  • 3
  • 3
Immunohistochemistry (IHC)

Clone

2F12D3
  • Characteristics

    Monoclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein corresponding to Mouse collagen II

    Isotype

    IgG
  • Application Notes

    IHC 1:300-1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    2.6 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 1 % BSA and 50 % glycerol, pH 7.4

    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

    COL2A1 (Collagen, Type II, alpha 1 (COL2A1))

    Alternative Name

    COL2A1

    Background

    This gene encodes the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene.

    UniProt

    P28481

    Pathways

    Sensory Perception of Sound, Growth Factor Binding
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