GSC2 Polyclonal Antibody
€0.00
In stock
SKU
ELK-ES2484
Catalog Number: ELK-ES2484
Reactivity: Human, Mouse
Applications: WB, ELISA
Information
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Questions? Contact us!
Reactivity: Human, Mouse
Applications: WB, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Background:
goosecoid homeobox 2(GSC2) Homo sapiens 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],
Alternative Names:
GSC2, GSCL, Homeobox protein goosecoid-2, GSC-2, Homeobox protein goosecoid-like, GSC-L
Immunogen: The antiserum was produced against synthesized peptide derived from human GSC2. AA range:131-180
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 25
GeneID: GSC2
Storage: -20°C/1 year
NOTE: For Research Use Only
goosecoid homeobox 2(GSC2) Homo sapiens 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],
Alternative Names:
GSC2, GSCL, Homeobox protein goosecoid-2, GSC-2, Homeobox protein goosecoid-like, GSC-L
Immunogen: The antiserum was produced against synthesized peptide derived from human GSC2. AA range:131-180
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 25
GeneID: GSC2
Storage: -20°C/1 year
NOTE: For Research Use Only
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