GSC2 antibody (AA 100-180)

Catalog No. ABIN7215174

This Rabbit Polyclonal antibody specifically detects GSC2 in WB and ELISA. It exhibits reactivity toward Human and Mouse.

Quick Overview for GSC2 antibody (AA 100-180) (ABIN7215174)

Target: GSC2 (Goosecoid Homeobox 2 (GSC2))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GSC2 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-GSC2 Antibody

Binding Specificity: AA 100-180

Purpose: GSC2 Polyclonal Antibody

Specificity: 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

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

Isotype: IgG

Application Details

Application Notes: 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.

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: 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.

Target Details for GSC2

Target: GSC2 (Goosecoid Homeobox 2 (GSC2))

Alternative Name: GSC2

Background: 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

Molecular Weight: observerd band 25kDa

Gene ID: 2928

UniProt: O15499