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COMP anticorps

Cet anticorps anti-COMP est un anticorps Lapin Polyclonal détectant COMP dans WB et IF. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7261762

Aperçu rapide pour COMP anticorps (ABIN7261762)

Antigène

Voir toutes COMP Anticorps
COMP (Cartilage Oligomeric Matrix Protein (COMP))

Reactivité

  • 48
  • 23
  • 16
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 65
  • 10
  • 1
  • 1
Lapin

Clonalité

  • 67
  • 10
Polyclonal

Conjugué

  • 39
  • 11
  • 6
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp COMP est non-conjugé

Application

  • 68
  • 29
  • 22
  • 16
  • 15
  • 13
  • 13
  • 6
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human COMP (NP_000086.2).

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000 IF 1:10-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    COMP (Cartilage Oligomeric Matrix Protein (COMP))

    Autre désignation

    COMP

    Sujet

    The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Contraction or expansion of a 5 aa aspartate repeat and other mutations can cause pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED).

    Poids moléculaire

    Observed_MW: 110 kDa

    Calculated_MW: 77 kDa/82 kDa

    ID gène

    1311

    UniProt

    P49747
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