Glypican 3 anticorps

N° du produit ABIN7091174

Cet anticorps anti-Glypican 3 est un anticorps Lapin Monoclonal détectant Glypican 3 dans FACS, IF, WB et ICC. Adapté pour Humain.

Aperçu rapide pour Glypican 3 anticorps (ABIN7091174)

Antigène: Glypican 3 (GPC3)

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp Glypican 3 est non-conjugé

Application: Flow Cytometry (FACS), Immunofluorescence (IF), Western Blotting (WB), Immunocytochemistry (ICC)

Clone: G8A2

Détail du produit anti-Glypican 3 anticorps

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human Glypican 3

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
FCM 1:20-100
IF()
ICC 1:100-500

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur Glypican 3

Antigène: Glypican 3 (GPC3)

Autre désignation: Glypican 3

Sujet:

Synonyms: GPC3, glypican3, glypican-3, Intestinal protein OCI-5, GTR2-2, MXR7.Intestinal protein OCI-5, GPC3_HUMAN.

Background: Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

ID gène: 2719

UniProt: P51654

Pathways: Glycosaminoglycan Metabolic Process