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anti-Human PITX2 Anticorps:
anti-Mouse (Murine) PITX2 Anticorps:
anti-Rat (Rattus) PITX2 Anticorps:
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Human Monoclonal PITX2 Primary Antibody pour IF, ELISA - ABIN562251
Acharya, Lingenfelter, Huang, Gage, Walter: Human PRKC apoptosis WT1 regulator is a novel PITX2-interacting protein that regulates PITX2 transcriptional activity in ocular cells. dans The Journal of biological chemistry 2009
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Horse (Equine) Polyclonal PITX2 Primary Antibody pour WB - ABIN2779638
Holmberg, Ingner, Johansson, Leander, Hjalt: PITX2 gain-of-function induced defects in mouse forelimb development. dans BMC developmental biology 2008
Cow (Bovine) Polyclonal PITX2 Primary Antibody pour IHC, WB - ABIN2776373
Martin, Skidmore, Philips, Vieira, Gage, Condie, Raphael, Martinez, Camper: PITX2 is required for normal development of neurons in the mouse subthalamic nucleus and midbrain. dans Developmental biology 2004
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This study for the first time demonstrates that the PITX2 mutation could lead to non-syndromic orodental anomalies in humans. We propose that the specific location in the C-terminal domain of PITX2 is exclusively necessary for tooth development.
Rs17042171, near PITX2 on chromosome 4q25, is associated with atrial fibrillation susceptibility in the Chinese Han population from the central plains, suggesting that this SNP can provide a new strategy for clinical diagnosis in atrial fibrillation patients.
NMR methodology was employed for determining the dynamics of lysine side-chain amino groups via (15)N relaxation measurements in the Lys50-class homeodomains from the Drosophila protein Bicoid and the human protein Pitx2
Results demonstrate that BBP (Montrer TP53BP2 Anticorps) decreases endometrial mesenchymal stem/stromal cell (EN-MSC (Montrer MSC Anticorps)) myogenic differentiation through up-regulation of miR (Montrer MLXIP Anticorps)-137 and decreased transcription of PITX2. Also, BBP (Montrer TP53BP2 Anticorps) affects PITX2 expression through miR (Montrer MLXIP Anticorps)-137 targeting the 3' untranslated region of PITX2 mRNA.
For non-metastatic triple-negative breast cancer patients, selective determination of the PITX2 DNA-methylation (Montrer HELLS Anticorps) status may serve as a cancer biomarker for predicting response to anthracycline-based adjuvant chemotherapy.
MiR (Montrer MLXIP Anticorps)-21 was down-regulated while PITX2 was up-regulated in pituitary adenoma tissues; MiR (Montrer MLXIP Anticorps)-21 can inhibit pituitary adenoma cell HP75 proliferation and facilitate apoptosis via inhibiting PITX2 expression
PITX2 and PANCR methylation status were shown to be independent predictors for overall survival in HNSCC patients. Tissue-based methylation testing could therefore potentially be employed to identify patients with a high risk for death who might benefit from a more radical or alternative treatment.
Data suggest that mutations affecting conserved non-coding elements of PITX2 may constitute an important class of mutations in patients with ASD (Montrer ARSD Anticorps) for whom the molecular cause of their disease have not yet been identified.
we propose that the Smad4 (Montrer SMAD4 Anticorps)-Pitx2-PPP2R2A (Montrer PPP2R2A Anticorps) axis, a new signaling pathway, suppresses the pancreatic carcinogenesis
Pitx2 is essential to maintain iHepSCs stem cell characteristics
data demonstrate that HTD, but not HTN, can impair Pitx2>>Wnt (Montrer WNT2 Anticorps) pathway providing thus a molecular link to AF
Defined a transcriptional architecture for atrial rhythm control organized as an incoherent feed-forward loop, driven by TBX5 (Montrer TBX5 Anticorps) and modulated by PITX2. TBX5 (Montrer TBX5 Anticorps)/PITX2 interplay provides tight control of atrial rhythm effector gene expression, and perturbation of the co-regulated network caused atrial fibrillation susceptibility.
Uncovering a Pitx2-Sox2 (Montrer SOX2 Anticorps)-Lef-1 (Montrer LEF1 Anticorps) transcriptional mechanism that regulates dental epithelial stem cells homeostasis and dental development.
Study reports that p27 (Montrer CDKN1B Anticorps) normally exerts a negative feedback on p21 (Montrer D4S234E Anticorps) expression: p27 (Montrer CDKN1B Anticorps) directly represses the expression of the transcription factor Pitx2 which in turn maintains decreased p21 (Montrer D4S234E Anticorps) levels. Consequently, in cells lacking p27 (Montrer CDKN1B Anticorps), de-repression of Pitx2 causes the up-regulation of p21 (Montrer D4S234E Anticorps) showing a new mechanism by which p27 (Montrer CDKN1B Anticorps) regulates cell cycle progression by transcriptionally regulating the expression of Pitx2 and p21 (Montrer D4S234E Anticorps).
demonstrate a dose-dependent relation between Pitx2 expression and the expression of atrial fibrillation susceptibility genes
Data suggest a putative role of the homeobox protein PITX2 (PITX2B) isoform during ventricular septation as well as in the maturation of the right portion of the atrioventricular canal.
Pitx2 represses left-side expression of a conserved lncRNA Playrr. Pitx2 auto-regulation directs chromatin topology to coordinate left-right transcription and organogenesis.
The AP-2beta (Montrer TFAP2B Anticorps) transcription factor is an important effector of PITX2 function during corneal development, required for differentiation of corneal endothelium and establishment of angiogenic privilege.
Pitx2-deficient neonatal mouse hearts failed to repair after apex (Montrer APEX1 Anticorps) resection, whereas adult mouse cardiomyocytes with Pitx2 gain-of-function efficiently regenerated after myocardial infarction
Late zygotic oep (Montrer TDGF1 Anticorps) mutants have strongly reduced or absent pitx2 expression in the lateral plate mesoderm (LPM), but this expression can be rescued to strong levels by restoring oep (Montrer TDGF1 Anticorps) in midline structures only.
asymmetric expression of fatty acid elongase 6 gene is controlled by left right Nodal signaling and is independent of Pitx2 function in zebrafish
This study found PITX2 to be decreased in patients with sustained Atrial Fibrillation, suggesting a PITX2 loss of function mechanism in Atrial Fibrillation.
Antagonism between Nodal and Pitx2c activities sets an upper limit on parapineal cell numbers. Restricting parapineal cell number is crucial for the correct elaboration of epithalamic asymmetry.
Pitx2, implicated in left-right asymmetry, possessed appropriate 'atypical' Pegasus (Montrer IKZF5 Anticorps) binding sites in its promoter.
Data indicate that retinoic acid (RA) induces the expression patterns of genes normally expressed in the posterior tooth-forming region, such as pitx2 and dlx2b.
Pitx2 is essential for proper eye and craniofacial development in zebrafish.
Retinoic acid regulation of pitx2 is essential for coordinating interactions among neural crest, mesoderm, and developing eye.
Zebrafish pitx2 demonstrates conserved expression during ocular and craniofacial development. Thirteen conserved noncoding sequences positioned within a gene desert as far as 1.1 Mb upstream of the human PITX2
ESR1 (Montrer ESR1 Anticorps) inhibits the expression of Pitx2 gene by binding to a left side-specific enhancer region in Pitx2 gene and recruiting histone deacetylase 1 (Montrer HDAC1 Anticorps) to this region, leading to the suppression of Pitx2 gene in the left lateral plate mesoderm.
A novel spliced variant of cattle PITX2 was identified. In addition, a 24bp deletion detected in the PITX2 gene was found to have significant associations with cattle growth traits.
This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. The encoded protein acts as a transcription factor and regulates procollagen lysyl hydroxylase gene expression. This protein plays a role in the terminal differentiation of somatotroph and lactotroph cell phenotypes, is involved in the development of the eye, tooth and abdominal organs, and acts as a transcriptional regulator involved in basal and hormone-regulated activity of prolactin. Mutations in this gene are associated with Axenfeld-Rieger syndrome, iridogoniodysgenesis syndrome, and sporadic cases of Peters anomaly. A similar protein in other vertebrates is involved in the determination of left-right asymmetry during development. Alternatively spliced transcript variants encoding distinct isoforms have been described.
ALL1-responsive protein ARP1
, all1-responsive gene 1
, homeobox protein PITX2
, paired-like homeodomain transcription factor 2
, pituitary homeobox 2
, rieg bicoid-related homeobox transcription factor 1
, BRX1 homeoprotein
, orthodenticle-like homeobox 2
, paired-like homeodomain transcription factor Munc 30
, paired-like homeodomain transcription factor 2a
, homeodomain transcription factor 2
, transcription factor Pitx2
, homeodomain transcription factor Pitx2