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Complement C2 anticorps (AA 265-612)

L’anticorps Lapin Polyclonal anti-Complement C2 a été validé pour WB et IF. Il convient pour détecter Complement C2 dans des échantillons de Humain.
N° du produit ABIN1886288

Aperçu rapide pour Complement C2 anticorps (AA 265-612) (ABIN1886288)

Antigène

Voir toutes Complement C2 Anticorps
Complement C2

Reactivité

  • 59
  • 12
  • 11
  • 8
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 52
  • 9
  • 1
  • 1
Lapin

Clonalité

  • 55
  • 8
Polyclonal

Conjugué

  • 36
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Complement C2 est non-conjugé

Application

  • 35
  • 20
  • 13
  • 13
  • 11
  • 9
  • 6
  • 5
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Épitope

    • 15
    • 11
    • 6
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 265-612

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 265 and 612 of Human C2
  • Indications d'application

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Antigène

    Complement C2

    Sujet

    Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system.Activated C1 cleaves C2 into C2a and C2b.The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase.Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration.This gene localizes within the class III region of the MHC on the short arm of chromosome 6.Alternative splicing results in multiple transcript variants encoding distinct isoforms.Additional transcript variants have been described in publications but their full-length sequence has not been determined.

    Poids moléculaire

    83 kDa

    ID gène

    717

    NCBI Accession

    NP_000054, NM_000063
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