Fibromodulin anticorps (AA 19-376)

N° du produit ABIN7825376

Cet anticorps anti-Fibromodulin est un anticorps Lapin Polyclonal détectant Fibromodulin dans WB, ELISA et FACS. Adapté pour Humain et Souris.

Aperçu rapide pour Fibromodulin anticorps (AA 19-376) (ABIN7825376)

Antigène: Fibromodulin (FMOD)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Fibromodulin est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Détail du produit anti-Fibromodulin anticorps

Épitope: AA 19-376

Fonction: Anti-Fibromodulin/FMOD Antibody

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

Attributs du produit: Anti-Fibromodulin/FMOD Antibody catalog # A05030-1. Tested in WB, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

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: Western blot, 0.25-0.5 μg/mL, Human, Mouse
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Détails sur Fibromodulin

Antigène: Fibromodulin (FMOD)

Autre désignation: FMOD

Sujet: 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: 60-70 kDa

ID gène: 2331

UniProt: Q06828

Pathways: Glycosaminoglycan Metabolic Process