Fibromodulin anticorps (AA 19-376) (PE)

N° du produit ABIN7990794

Cet anticorps Lapin Polyclonal détecte spécifiquement Fibromodulin dans FACS. Il présente une réactivité avec des échantillons de Humain et Souris.

Aperçu rapide pour Fibromodulin anticorps (AA 19-376) (PE) (ABIN7990794)

Antigène: Fibromodulin (FMOD)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Fibromodulin est conjugé à/à la PE

Application: Flow Cytometry (FACS)

Détail du produit anti-Fibromodulin anticorps (PE)

Épitope: AA 19-376

Fonction: Anti-Fibromodulin/FMOD Antibody PE Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human Fibromodulin,FMOD shares 93.3% amino acid (aa) sequence identity with both mouse,rat Fibromodulin,FMOD.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human Fibromodulin/FMOD recombinant protein (Position: Q19-I376). Human Fibromodulin/FMOD shares 93.3% amino acid (aa) sequence identity with both mouse and rat Fibromodulin/FMOD.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur Fibromodulin

Antigène: Fibromodulin (FMOD)

Autre désignation: FMOD

Sujet:

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.

Gene Full Name: fibromodulin

ID gène: 2331

UniProt: Q06828

Pathways: Glycosaminoglycan Metabolic Process