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The protein encoded by TCF12 is a member of the basic helix-loop-helix (bHLH) E-protein family that recognizes the consensus binding site (E-box) CANNTG. De plus, nous expédions TCF12 Anticorps (92) et TCF12 Protéines (7) et beaucoup plus de produits pour cette protéine.
Heb expression is regulated by Med19 (Montrer MED19 Kits ELISA) in breast cancer cells.
enforced expression of transcription factor 12 suppressed cell proliferation, migration, and invasion in vitro and inhibited tumor growth in vivo. In conclusion, transcription factor 12 protein may be a novel molecule which plays a critical role in prostate cancer progression and patients' prognosis, suggesting it might be a promising therapeutic target for prostate cancer therapy
HEB may be involved in GBM cell proliferation, as HEB silencing reduced proliferation in cells cultured as monolayers or neurospheres. Furthermore, the results suggested a potential role for HEB in the maintenance of GBM stem cells, as HEB silencing affected the differentiation capacity of cells.
Two novel translocations leading to the inactivation of RUNX1 (Montrer RUNX1 Kits ELISA) and its partners SIN3A and TCF12 in myeloid leukemia (Montrer BCL11A Kits ELISA).
Studies suggest that transcription factor 12 (TCF12) should be included in level 2 genetic testing.
show that these mutations compromise TCF12 transcriptional activity and are associated with a more aggressive tumour type
several familial cases of coronal synostosis associated with mutations in TCF12
In t(8;21) leukemia cells, the two E proteins, HEB and E2A (Montrer TCF3 Kits ELISA), function as components of the stable AML1 (Montrer RUNX1 Kits ELISA)-ETO (Montrer RUNX1T1 Kits ELISA)-containing transcription factor complex (AETFC). The AETFC components cooperatively regulate gene expression and contribute to leukemogenesis.
haploinsufficiency of TCF12 causes coronal synostosis in humans and that severe bilateral coronal synostosis occ (Montrer TWIST1 Kits ELISA)urs in mice with 50% of the wild-type dosage of both the T (Montrer TWIST1 Kits ELISA)cf12 and Twist1 genes highlights the key role of TCF12 acting with TWIST1.
the CD91 (Montrer LRP1 Kits ELISA)/IKK (Montrer CHUK Kits ELISA)/NF-kappaB (Montrer NFKB1 Kits ELISA) signaling cascade is involved in secreted HSP90alpha-induced TCF12 expression, leading to E-cadherin (Montrer CDH1 Kits ELISA) down-regulation and enhanced CRC (Montrer CALR Kits ELISA) cell migration/invasion
we identified transcription factor TCF12 as a new target of miR (Montrer MLXIP Kits ELISA)-211 in oral squamous cell carcinoma
HEB (Montrer FREM1 Kits ELISA) is a fundamental link between Nodal signalling, the derepression of a specific class of poised promoters during differentiation, and lineage specification in mouse embryonic stem cells
severe bilateral coronal synostosis occurs in mice with 50% of the wild-type dosage of both the Tcf12 and Twist1 (Montrer TWIST1 Kits ELISA) genes highlights the key role of TCF12 acting with TWIST1 (Montrer TWIST1 Kits ELISA) in the normal development of the coronal sutures
Deficiency in the E proteins, E2A (Montrer TCF3 Kits ELISA) and HEB (Montrer FREM1 Kits ELISA), led to increased frequency of terminally differentiated effector KLRG1 (Montrer KLRG1 Kits ELISA)(hi) CD8 (Montrer CD8A Kits ELISA)(+) T cells in mice during infection, and decreased generation of longer-lived memory-precursor cells during the immune response.
Deletion of HEB (Montrer FREM1 Kits ELISA) and E2A (Montrer TCF3 Kits ELISA) in DP thymocytes specifically blocked the development of CD4 (Montrer CD4 Kits ELISA)(+) lineage T cells. Furthermore, deletion of the E protein inhibitors Id2 and Id3 (Montrer ID3 Kits ELISA) allowed CD4 (Montrer CD4 Kits ELISA)(+) T cell development but blocked CD8 (Montrer CD8A Kits ELISA)(+) lineage development.
the earliest event in B-cell specification involves the induction of FOXO1 (Montrer FOXO1 Kits ELISA) expression and requires the combined activities of E2A (Montrer TCF3 Kits ELISA) and HEB (Montrer FREM1 Kits ELISA)
These results showed a new set of interactions between HEB (Montrer FREM1 Kits ELISA), Notch1 (Montrer NOTCH1 Kits ELISA), and GATA3 (Montrer GATA3 Kits ELISA) that regulate the T-cell fate choice in developing thymocytes.
Developmental progression of fetal HEB (Montrer FREM1 Kits ELISA)(-/-) precursors to the pre-T-cell stage is restored by HEBAlt.
HEB (Montrer FREM1 Kits ELISA) is a specific and essential factor in T-cell development and in the generation of the iNKT cell lineage.
the dosage of HEB (Montrer FREM1 Kits ELISA) determines pT alpha (Montrer PTCRA Kits ELISA) gene expression in immature T cells
The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH) E-protein family that recognizes the consensus binding site (E-box) CANNTG. This encoded protein is expressed in many tissues, among them skeletal muscle, thymus, B- and T-cells, and may participate in regulating lineage-specific gene expression through the formation of heterodimers with other bHLH E-proteins. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
transcription factor 12
, transcription factor 12 (HTF4, helix-loop-helix transcription factors 4)
, DNA-binding protein HTF4
, E-box-binding protein
, class B basic helix-loop-helix protein 20
, helix-loop-helix transcription factor 4
, transcription factor HTF-4
, class A helix-loop-helix transcription factor ME1
, SCBP alpha
, salivary-specific cAMP response element-binding protein alpha
, basic helix-loop-helix protein
, class A helix-loop-helix transcription factor GE1