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TBX1 Rabbit anti-Human, Polyclonal Antibody, Abnova™
Descripción
This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98% amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq
Especificaciones
Especificaciones
| Antígeno | TBX1 |
| Aplicaciones | Immunofluorescence, Western Blot |
| Clasificación | Polyclonal |
| Conjugado | Unconjugated |
| Descripción | Rabbit polyclonal antibody raised against synthetic peptide of TBX1. |
| Dilución | Western Blot (1:500-1:1000) Immunofluorescence (1:500-1:1000) ELISA (1:20000) The optimal working dilution should be determined by the end user. |
| Formulación | In PBS, pH 7.4 (150mM NaCl, 0.02% sodium azide, 50% glycerol) |
| génica | TBX1 |
| Alias de gen | CAFS/CTHM/DGCR/DGS/DORV/TBX1C/TGA/VCFS |
| Símbolos de los genes | TBX1 |
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For Research Use Only
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