Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

Fibulin 5 anticorps

Cet anticorps anti-Fibulin 5 est un anticorps Lapin Polyclonal détectant Fibulin 5 dans WB et IF. Adapté pour Humain et Souris.
N° du produit ABIN7264982

Aperçu rapide pour Fibulin 5 anticorps (ABIN7264982)

Antigène

Voir toutes Fibulin 5 (FBLN5) Anticorps
Fibulin 5 (FBLN5)

Reactivité

  • 65
  • 35
  • 27
  • 1
Humain, Souris

Hôte

  • 61
  • 10
  • 1
Lapin

Clonalité

  • 60
  • 14
Polyclonal

Conjugué

  • 32
  • 9
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Fibulin 5 est non-conjugé

Application

  • 55
  • 28
  • 18
  • 9
  • 5
  • 4
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human FBLN5 (NP_006320.2).

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000 IF 1:50-1:100

    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

    Fibulin 5 (FBLN5)

    Autre désignation

    FBLN5

    Sujet

    The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3).

    Poids moléculaire

    Observed_MW: 72 kDa

    Calculated_MW: 50 kDa

    ID gène

    10516

    UniProt

    Q9UBX5

    Pathways

    SARS-CoV-2 Protein Interactome
Vous êtes ici:
Chat with us!