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Fibromodulin anticorps

L’anticorps Lapin Polyclonal anti-Fibromodulin a été validé pour WB, IHC et ELISA. Il convient pour détecter Fibromodulin dans des échantillons de Humain, Rat et Souris.
N° du produit ABIN7114223

Aperçu rapide pour Fibromodulin anticorps (ABIN7114223)

Antigène

Voir toutes Fibromodulin (FMOD) Anticorps
Fibromodulin (FMOD)

Reactivité

  • 56
  • 28
  • 22
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 49
  • 9
  • 2
Lapin

Clonalité

  • 53
  • 7
Polyclonal

Conjugué

  • 27
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Fibromodulin est non-conjugé

Application

  • 48
  • 23
  • 22
  • 13
  • 13
  • 13
  • 6
  • 6
  • 5
  • 3
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Fonction

    FMOD antibody

    Purification

    Immunogen affinity purified

    Pureté

    ≥95 % as determined by SDS-PAGE

    Immunogène

    fibromodulin

    Isotype

    IgG
  • Indications d'application

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 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.

    Conseil sur la manipulation

    Avoid repeated freeze / thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    -20°C for 12 months

    Date de péremption

    12 months
  • Antigène

    Fibromodulin (FMOD)

    Autre désignation

    FMOD

    Sujet

    Synonyms: Fibromodulin (FM)|Collagen-binding 59 kDa protein|Keratan sulfate proteoglycan fibromodulin (KSPG fibromodulin)|FMOD|FM|SLRR2E

    Background: Fibromodulin belongs to the family of small interstitial proteoglycans. The encoded protein possesses a central region containing leucine-rich repeats with 4 keratan sulfate chains, flanked by terminal domains containing disulphide bonds. Owing to the interaction with type I and type II collagen fibrils and in vitro inhibition of fibrillogenesis, the encoded protein may play a role in the assembly of extracellular matrix. It may also regulate TGF-beta activities by sequestering TGF-beta into the extracellular matrix. Sequence variations in this gene may be associated with the pathogenesis of high myopia. Alternative splicing results in multiple transcript variants.

    Poids moléculaire

    45 kDa

    ID gène

    2331

    UniProt

    Q06828

    Pathways

    Glycosaminoglycan Metabolic Process
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