Versican anticorps

N° du produit ABIN7271309

Détail du produit anti-Versican anticorps

Antigène: Versican (Vcan)

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp Versican est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Fonction: Versican Rabbit mAb

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Monoclonal Antibodies

Purification: Affinity purification

Immunogène: A synthesized peptide derived from human Versican

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,0.05 % BSA,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.

Détails sur Versican

Antigène: Versican (Vcan)

Autre désignation: VCAN (Vcan Produits)

Synonymes: anticorps br146, anticorps cspg2, anticorps cspg2a, anticorps sb:cb63, anticorps versican, anticorps CSPG2, anticorps Cspg2, anticorps wgn, anticorps ervr, anticorps pg-m, anticorps wgn1, anticorps Xversican, anticorps dcan, anticorps cspg2b, anticorps fb99b07, anticorps wu:fb99b07, anticorps ERVR, anticorps GHAP, anticorps PG-M, anticorps WGN, anticorps WGN1, anticorps 5430420N07Rik, anticorps 9430051N09, anticorps DPEAAE, anticorps NG2, anticorps PG-M(V0), anticorps PG-M(V1), anticorps hdf, anticorps versican a, anticorps versican, anticorps versican b, anticorps vcana, anticorps VCAN, anticorps Vcan, anticorps vcan, anticorps vcanb

Sujet: This gene is a member of the aggrecan/versican proteoglycan family. The protein encoded is a large chondroitin sulfate proteoglycan and is a major component of the extracellular matrix. This protein is involved in cell adhesion, proliferation, proliferation, migration and angiogenesis and plays a central role in tissue morphogenesis and maintenance. Mutations in this gene are the cause of Wagner syndrome type 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009],CSPG2, ERVR, GHAP, PG-M, WGN, WGN1,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,Signal Transduction,VCAN

Poids moléculaire: 373kDa

ID gène: 1462

UniProt: P13611

Pathways: Glycosaminoglycan Metabolic Process