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Collagen Type I Antikörper

Dieses Maus Monoklonal-Antikörper erkennt spezifisch Collagen Type I in ELISA und IHC. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7112980

Kurzübersicht für Collagen Type I Antikörper (ABIN7112980)

Target

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

Reaktivität

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

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

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

Klon

3D7
  • Aufreinigung

    protein A+G purified

    Reinheit

    ≥95 % as determined by SDS-PAGE

    Immunogen

    collagen, type I, alpha 2

    Isotyp

    IgG1
  • Applikationshinweise

    IHC: 1:2000 - 1:8000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    Haltbarkeit

    12 months
  • Target

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

    Andere Bezeichnung

    Collagen Type I

    Hintergrund

    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.

    Gen-ID

    1278

    UniProt

    P08123
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