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TBX6 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. Additionally we are shipping T-Box 6 Proteins (4) and many more products for this protein.
Showing 10 out of 72 products:
Human Polyclonal TBX6 Primary Antibody for EIA, WB - ABIN955114
Fei, Wu, Wang, Zhou, Wang, Ding, Wang, Qiu: The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population. in Spine 2010
Show all 5 references for 955114
Cow (Bovine) Polyclonal TBX6 Primary Antibody for IHC, WB - ABIN2777918
Papapetrou, Putt, Fox, Edwards: The human TBX6 gene: cloning and assignment to chromosome 16p11.2. in Genomics 1999
Show all 3 references for 2777918
Cow (Bovine) Polyclonal TBX6 Primary Antibody for WB - ABIN2777917
Blin, Nury, Stefanovic, Neri, Guillevic, Brinon, Bellamy, Rücker-Martin, Barbry, Bel, Bruneval, Cowan, Pouly, Mitalipov, Gouadon, Binder, Hagège, Desnos, Renaud, Menasché, Pucéat: A purified population of multipotent cardiovascular progenitors derived from primate pluripotent stem cells engrafts in postmyocardial infarcted nonhuman primates. in The Journal of clinical investigation 2010
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Mutations of RBM8A (show RBM8A Antibodies) and TBX6 are associated with disorders of the mullerian ducts.
Compound inheritance of a rare null mutation and a hypomorphic allele of TBX6 accounted for up to 11% of congenital scoliosis cases in the series that we analyzed.
Data have identified TBX6 as a new gene associated with Mullerian aplasia. The results also support the relevance of LHX1 (show LHX1 Antibodies) and CNVs in the development of this congenital malformation.
we have used exome capture and next-generation sequencing to identify a stoploss mutation in TBX6 that segregates with disease in two generations of one family.
first report on single nucleotide polymorphisms of TBX6 gene in congenital scoliosis (CS) that suggests genetic variants of TBX6 gene is associated with CS in the Chinese Han population.
Tbx18 (show TBX18 Antibodies) interacts with Gata4 (show GATA4 Antibodies) and Nkx2-5 (show NKX2-5 Antibodies) and competes Tbx5 (show TBX5 Antibodies)-mediated activation of the cardiac Natriuretic peptide precursor type a-promoter. Tbx18 (show TBX18 Antibodies) down-regulates Tbx6-activated Delta-like 1 (show DLL1 Antibodies) expression in the somitic mesoderm in vivo
Segmental border is defined by Ripply2 (show RIPPLY2 Antibodies)-mediated Tbx6 repression independent of Mesp2 (show Mesp2 Antibodies).
Tbx6 and the Wnt (show WNT2 Antibodies) pathway cooperatively regulate proper Hes7 (show HES7 Antibodies) expression.
Tbx6 is required for cardiac myocyte differentiation and represses neural differentiation in the P19CL6 model.
Tbx6 acts in the mesoderm where it has a dual function. It promotes differentiation of cells into paraxial mesoderm, and it suppresses neural cell fate specification by repressing Sox2 (show SOX2 Antibodies).
Tbx6 represses Sox2 (show SOX2 Antibodies) by inactivating enhancer N1 to inhibit neural development, and this is an essential step for the specification of paraxial mesoderm from the axial stem cells.
determined the phenotypic and molecular consequences of ectopically expressing Tbx6 within the segmented paraxial mesoderm and its derivatives using a 3-component transgenic system
Data show that partial restoration of Tbx6 expression in null mutants rescues somite development, and that Tbx6 activity in the paraxial mesoderm is also required for their normal patterning.
Contol of Tbx6 gene expression during development.
uncovered four putative Tbx6 binding sites within a delta-like 1 (show DLL1 Antibodies) paraxial mesoderm enhancer
Tbx6 directly binds to the Mesp2 (show Mesp2 Antibodies) gene upstream region and mediates Notch (show NOTCH1 Antibodies) signaling, and subsequent Mesp2 (show Mesp2 Antibodies) transcription, in the anterior presomitic mesoderm.
Tbx6 is required for neural crest and intermediate mesoderm development in Xenopus
several signaling pathways are involved in regulating Tbx6 expression in the initiation of myogenesis
FGF8 (show FGF8 Antibodies), Wnt8 (show WNT8A Antibodies) and Myf5 (show MYF5 Antibodies) are target genes of Tbx6 during anteroposterior specification in Xenopus embryo
Data show that morpholino-induced knockdown of Xenopus Tbx6 impairs posterior development, indicating the requirement of XTbx6 in this process.
Based on our findings, we conclude that a part of the transcriptional repression at the anterior end of the PSM (show SH2B1 Antibodies) is caused by Bowline mediated transcriptional repression of Tbx6-dependent gene expression in X. laevis.
Tbx6, thylacine 1, and E47 synergistically activate bowline expression in Xenopus somitogenesis.
These results indicate that the appropriate expression of bowline/Ripply2 is regulated by a direct interaction between the Tbx6 and mespb proteins during Xenopus somitogenesis.
Xtbx6 is a direct regulator of pMesogenin1 (show MSGN1 Antibodies) and 2, which are both involved in somitogenesis and myogenesis including that of body wall muscle in Xenopus laevis
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. Knockout studies in mice indicate that this gene is important for specification of paraxial mesoderm structures.
, T-box protein 6
, T-box transcription factor TBX6