GSC2 anticorps (AA 100-180)

N° du produit ABIN7215174

Cet anticorps Lapin Polyclonal détecte spécifiquement GSC2 dans WB et ELISA. Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour GSC2 anticorps (AA 100-180) (ABIN7215174)

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 100-180

Fonction: GSC2 Polyclonal 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

Immunogène: Synthesized peptide derived from the C-terminal region of human GSC2 at AA range: 100-180

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:20000). Not yet tested in other applications.

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur GSC2

Antigène: GSC2 (Goosecoid Homeobox 2 (GSC2))

Autre désignation: GSC2

Sujet: Rabbit Anti-GSC2 Polyclonal Antibody,GSC2, GSCL, Homeobox protein goosecoid-2, GSC-2, Homeobox protein goosecoid-like, GSC-L,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. GSC2 is expressed in a limited number of adult tissues, as well as in early human development.,Homeobox protein goosecoid-2

Poids moléculaire: observerd band 25kDa

ID gène: 2928

UniProt: O15499