GSC2 anticorps (AA 131-180)

N° du produit ABIN1533500

Cet anticorps anti-GSC2 Polyclonal Lapin (ABIN1533500) détecte spécifiquement GSC2 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour GSC2 anticorps (AA 131-180) (ABIN1533500)

Antigène: GSC2 (Goosecoid Homeobox 2 (GSC2))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GSC2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-GSC2 anticorps

Épitope: AA 131-180

Fonction: GSC2 Antibody

Specificité: GSC2 Polyclonal Antibody detects endogenous levels of GSC2 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Pureté: > 95 %

Immunogène: The antiserum was produced against synthesized peptide derived from human GSC2. AA range:131-180

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000. ELISA: 1:20000. Not yet tested in other applications.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 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: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur GSC2

Antigène: GSC2 (Goosecoid Homeobox 2 (GSC2))

Autre désignation: GSC2

Sujet:

Synonyms: GSC2, GSCL, Homeobox protein goosecoid-2, GSC-2, Homeobox protein goosecoid-like, GSC-L

Background: Goosecoidlike (GSCL), a homeodomain-containing gene, resides in the critical region for VCFS/DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS/DGS derive from the pharyngeal arches of the developing embryo, it is believed that haploinsufficiency of a gene involved in embryonic development may be responsible for its etiology. The gene is expressed in a limited number of adult tissues, as well as in early human development. [provided by RefSeq, Jul 2008],

Gene Name: GSC2

Protein Name: Homeobox protein goosecoid-2

Poids moléculaire: 21 kDa

ID gène: 2928

OMIM: 601845

UniProt: O15499