Welcome to Omnimabs!
TEL: 02154156726 Info: info@Omnimabs.com CN

TBX1 antibody - middle region

Catalog Number:OM106335
OM106335
Discount Price
OM106335-100ul
1~2 Week
100ul
OM106335-50ul
50ul
OM106335-20ul
20ul
1~2 Week
Product Profile
Product Name TBX1 antibody - middle region
Antibody Type Primary Antibodies
Immunogen The immunogen for anti-TBX1 antibody: synthetic peptide directed towards the middle region of human TBX1
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications WB
Species Reactivity Guinea Pig,Human,Mouse,Rabbit,Rat
Concentration 1mg/ml
Purification Affinity purified
Target Information
Gene Symbol TBX1
Gene Synonyms CAFS
CTHM
DGCR
DGS
DORV
TBX1C
TGA
VCFS
Gene Full Name T-box 1
Gene Summary TBX1 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. TBX1 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 TBX1 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. 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.
Alternative Names CAFS
CTHM
DGCR
DGS
DORV
TBX1C
TGA
VCFS
Molecular Weight(MW) 43kDa
Sequence 398 amino acids
Database Links
Entrez Gene 6899
SwissProt ID O43435
Protein Accession NP_542377
Application

Western blot

0.2-1 ug/ml
ELISA Titer: 1:62500
Positive Control: Human Lung
Additional Information
Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
validation
question title
question detaiil
Verification code