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Collagen Type I antibody

This Mouse Monoclonal antibody specifically detects Collagen Type I in ELISA and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN7112980

Quick Overview for Collagen Type I antibody (ABIN7112980)

Target

See all Collagen Type I (COL1) Antibodies
Collagen Type I (COL1) (Collagen, Type I (COL1))

Reactivity

  • 96
  • 61
  • 55
  • 19
  • 18
  • 17
  • 15
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 65
  • 38
  • 13
Mouse

Clonality

  • 78
  • 38
Monoclonal

Conjugate

  • 58
  • 14
  • 6
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
This Collagen Type I antibody is un-conjugated

Application

  • 75
  • 40
  • 38
  • 31
  • 31
  • 27
  • 27
  • 24
  • 18
  • 17
  • 16
  • 13
  • 8
  • 5
  • 4
  • 4
  • 1
ELISA, Immunohistochemistry (IHC)

Clone

3D7
  • Purification

    protein A+G purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    collagen, type I, alpha 2

    Isotype

    IgG1
  • Application Notes

    IHC: 1:2000 - 1:8000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 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

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    Collagen Type I (COL1) (Collagen, Type I (COL1))

    Alternative Name

    Collagen Type I

    Background

    Synonyms:Alpha 2 type I collagen, COL1A2, Collagen alpha 2(I) chain, Collagen Type I, collagen, type I, alpha 2, OI4 Background:This gene encodes the pro-alpha2 chain of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIB, recessive Ehlers-Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan syndrome. Symptoms associated with mutations in this gene, however, tend to be less severe than mutations in the gene for the alpha1 chain of type I collagen (COL1A1) reflecting the different role of alpha2 chains in matrix integrity. Three transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene.

    Gene ID

    1278

    UniProt

    P08123
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