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Collagen Type I anticorps

Cet anticorps Souris Monoclonal détecte spécifiquement Collagen Type I dans WB, IHC (p) et EIA. Il présente une réactivité envers Humain et Souris.
N° du produit ABIN782308

Aperçu rapide pour Collagen Type I anticorps (ABIN782308)

Antigène

Voir toutes Collagen Type I (COL1) Anticorps
Collagen Type I (COL1) (Collagen, Type I (COL1))

Reactivité

  • 98
  • 60
  • 56
  • 19
  • 18
  • 17
  • 15
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 68
  • 38
  • 13
Souris

Clonalité

  • 81
  • 38
Monoclonal

Conjugué

  • 60
  • 15
  • 6
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Cet anticorp Collagen Type I est non-conjugé

Application

  • 77
  • 42
  • 38
  • 35
  • 31
  • 27
  • 26
  • 24
  • 18
  • 17
  • 17
  • 13
  • 11
  • 5
  • 4
  • 4
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Clone

3G3
  • Specificité

    Recognizes Collagen type I (COL1A1).

    Réactivité croisée (Details)

    Species reactivity (expected):Mouse.
    Species reactivity (tested):Human.

    Purification

    Protein A Chromatography

    Immunogène

    Recombinant Human COL1A1

    Isotype

    IgG3
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    PBS, pH 7.4

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène

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

    Autre désignation

    Collagen Type I

    Sujet

    Collagens are highly conserved throughout evolution and are characterised by an uninterrupted "Glycine X Y" triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor.Synonyms: Alpha-1 type I collagen, Alpha-2 type I collagen, COL1A1, COL1A2

    ID gène

    1277

    NCBI Accession

    NP_000079

    UniProt

    P02452
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