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Collagen Type I Antikörper

Dieses Maus Monoklonal-Antikörper erkennt spezifisch Collagen Type I in WB, IHC (p) und EIA. Er zeigt eine Reaktivität gegenüber Human und Maus.
Produktnummer ABIN782308

Kurzübersicht für Collagen Type I Antikörper (ABIN782308)

Target

Alle Collagen Type I (COL1) Antikörper anzeigen
Collagen Type I (COL1) (Collagen, Type I (COL1))

Reaktivität

  • 96
  • 60
  • 55
  • 19
  • 18
  • 17
  • 15
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Maus

Wirt

  • 65
  • 38
  • 13
Maus

Klonalität

  • 78
  • 38
Monoklonal

Konjugat

  • 58
  • 14
  • 6
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Dieser Collagen Type I Antikörper ist unkonjugiert

Applikation

  • 74
  • 41
  • 38
  • 32
  • 31
  • 27
  • 26
  • 24
  • 17
  • 17
  • 16
  • 13
  • 8
  • 5
  • 4
  • 4
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Klon

3G3
  • Spezifität

    Recognizes Collagen type I (COL1A1).

    Kreuzreaktivität (Details)

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

    Aufreinigung

    Protein A Chromatography

    Immunogen

    Recombinant Human COL1A1

    Isotyp

    IgG3
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    1.0 mg/mL

    Buffer

    PBS, pH 7.4

    Handhabung

    Avoid repeated freezing and thawing.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

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

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

    Andere Bezeichnung

    Collagen Type I

    Hintergrund

    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

    Gen-ID

    1277

    NCBI Accession

    NP_000079

    UniProt

    P02452
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