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anti-Human MED12 Anticorps:
anti-Mouse (Murine) MED12 Anticorps:
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Human Polyclonal MED12 Primary Antibody pour ICC, IF - ABIN250749
Tutter, Kowalski, Baltus, Iourgenko, Labow, Li, Kadam: Role for Med12 in regulation of Nanog and Nanog target genes. dans The Journal of biological chemistry 2009
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Human Polyclonal MED12 Primary Antibody pour ELISA, WB - ABIN564287
Rienzo, Casamassimi, Schiano, Grimaldi, Infante, Napoli: Distinct alternative splicing patterns of mediator subunit genes during endothelial progenitor cell differentiation. dans Biochimie 2012
Show all 2 Pubmed References
Human Polyclonal MED12 Primary Antibody pour ICC, IF - ABIN4333402
Pérot, Croce, Ribeiro, Lagarde, Velasco, Neuville, Coindre, Stoeckle, Floquet, MacGrogan, Chibon: MED12 alterations in both human benign and malignant uterine soft tissue tumors. dans PLoS ONE 2012
Study confirmed the association of MED12 mutations with smaller leiomyoma size, multiplicity and conventional hystotype, and revealed novel associations between the MED12-mutation status and leiomyoma location and parity.
High frequency of the MED12 mutation in uterine leiomyomas of South Korean patients.
The high rate of TERT (Montrer TERT Anticorps) promoter mutations, MED12 mutations, RBM10 (Montrer RBM10 Anticorps) mutations, and chromosome 1q gain highlight their likely association with tumor virulence
Role of MED12 as a tumor suppressor in other cancers to include CRC (Montrer CALR Anticorps), and suggest TGF-beta (Montrer TGFB1 Anticorps) signaling as a potential mediator of this effect.
High MED12 expression is associated with small cell lung cancer.
Data indicate that mediator complex subunit 12 (MED12) plays a central oncogenic role in breast fibroepithelial tumorigenesis.
MED12 mutation does not appear to represent a significant molecular alteration in this cohort of patients according to the analysis by the traditional "gold standard."
knockdown of MED12 was shown to confer resistance to apoptosis following pediatric T-cell acute lymphoblastic leukemia relevant chemotherapy drug treatment in Jurkat leukemia cells
Our findings provide new mechanistic insights into the MED12 functions and indicate that somatic nonsense mutations in early exons may avoid NMD.
With a strong genotype-phenotype correlation that is already known for MED12, this could be a new phenotype linked to MED12, thus expanding the phenotypic spectrum of MED12-related disorders.
Study provide evidence that Med12 regulates neural stem cell gene expression programs linked to adhesion and cell cycle progression but suppresses its adhesion by repressing the expression of cell adhesion molecules.
alterations in MED12-dependent enhancer regulation may control both physiological and malignant hematopoiesis.
The data reveal how the interplay between PRC1 (Montrer PRC1 Anticorps), ncRNA and Mediator complexes controls pluripotency and cellular differentiation.
Med1 and Med12, two subunits of the mediator complex implicated in transcription initiation and long-range enhancer/promoter loop formation, are dynamically recruited to the IgH locus enhancers.
leiomyomatous, Med12 c.131G>A variant-expressing uteri developed chromosomal rearrangements.
this work points to Med12 being an essential coregulator of transcription factors controlling neural tube closure.
show that in Med12 hypomorphic embryos, the Wnt (Montrer WNT2 Anticorps)/planar cell polarity pathway is disrupted and that canonical Wnt (Montrer WNT2 Anticorps)/beta-catenin (Montrer CTNNB1 Anticorps) signaling is impaired.
Nanog (Montrer NANOG Anticorps) and Med12 function in concert to regulate Nanog (Montrer NANOG Anticorps) target genes and identify a novel role for Med12 in embryonic stem cell regulation.
med12 mutants exhibit multiple defects in the development of the epithalamus, including failure of parapineal specification and disruption of cell differentiation and/or maintenance of specific cell types in the pineal organ and the habenula.
The kto/med12 mutation results in specific defects of boundary cell formation in the zebrafish hindbrain
critical targets of TRAP230 function may include proteins important for cell mobility, cell sorting, and tissue assembly
A critical function of the Trap230 subunit is shown for Sox9 (Montrer SOX9 Anticorps) as a coactivator; Trap230 also participates in Sox9 (Montrer SOX9 Anticorps)-independent transcriptional regulation.
reveal a regulatory role of motionless/Med12 in vertebrate neuronal development
Med12 modulates the ability of Casanova/Sox32 to induce sox17 expression in endodermal development.
The initiation of transcription is controlled in part by a large protein assembly known as the preinitiation complex. A component of this preinitiation complex is a 1.2 MDa protein aggregate called Mediator. This Mediator component binds with a CDK8 subcomplex which contains the protein encoded by this gene, mediator complex subunit 12 (MED12), along with MED13, CDK8 kinase, and cyclin C. The CDK8 subcomplex modulates Mediator-polymerase II interactions and thereby regulates transcription initiation and reinitation rates. The MED12 protein is essential for activating CDK8 kinase. Defects in this gene cause X-linked Opitz-Kaveggia syndrome, also known as FG syndrome, and Lujan-Fryns syndrome.
CAG repeat protein 45
, OPA-containing protein
, activator-recruited cofactor 240 kDa component
, human opposite paired
, mediator of RNA polymerase II transcription subunit 12
, mediator of RNA polymerase II transcription, subunit 12 homolog
, putative mediator subunit 12
, thyroid hormone receptor-associated protein complex 230 kDa component
, thyroid hormone receptor-associated protein, 230 kDa subunit
, trinucleotide repeat containing 11 (THR-associated protein, 230 kDa subunit)
, trinucleotide repeat-containing gene 11 protein
, trinucleotide repeat containing 11
, OPA-containing protein 1
, mediator complex subunit 12
, trinucleotide repeat containing 11 (THR-associated protein)
, protein kohtalo
, protein motionless
, thyroid hormone receptor-associated protein 230
, thyroid hormone receptor-associated protein complex component TRAP230