Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
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. Additionally we are shipping TCF12 Antibodies (92) and many more products for this protein.
Showing 7 out of 7 products:
Heb expression is regulated by Med19 (show MED19 Proteins) 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 (show RUNX1 Proteins) and its partners SIN3A (show SIN3A Proteins) and TCF12 in myeloid leukemia (show BCL11A Proteins).
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 (show TCF3 Proteins), function as components of the stable AML1 (show RUNX1 Proteins)-ETO (show RUNX1T1 Proteins)-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 (show TWIST1 Proteins)urs in mice with 50% of the wild-type dosage of both the T (show TWIST1 Proteins)cf12 and Twist1 genes highlights the key role of TCF12 acting with TWIST1.
the CD91 (show LRP1 Proteins)/IKK (show CHUK Proteins)/NF-kappaB (show NFKB1 Proteins) signaling cascade is involved in secreted HSP90alpha (show HSP90AA2 Proteins)-induced TCF12 expression, leading to E-cadherin (show CDH1 Proteins) down-regulation and enhanced CRC (show CALR Proteins) cell migration/invasion
we identified transcription factor TCF12 as a new target of miR (show MLXIP Proteins)-211 in oral squamous cell carcinoma
HEB 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 (show TWIST1 Proteins) genes highlights the key role of TCF12 acting with TWIST1 (show TWIST1 Proteins) in the normal development of the coronal sutures
Deficiency in the E proteins, E2A (show TCF3 Proteins) and HEB, led to increased frequency of terminally differentiated effector KLRG1 (show KLRG1 Proteins)(hi) CD8 (show CD8A Proteins)(+) T cells in mice during infection, and decreased generation of longer-lived memory-precursor cells during the immune response.
Deletion of HEB and E2A (show TCF3 Proteins) in DP thymocytes specifically blocked the development of CD4 (show CD4 Proteins)(+) lineage T cells. Furthermore, deletion of the E protein inhibitors Id2 and Id3 (show ID3 Proteins) allowed CD4 (show CD4 Proteins)(+) T cell development but blocked CD8 (show CD8A Proteins)(+) lineage development.
the earliest event in B-cell specification involves the induction of FOXO1 (show FOXO1 Proteins) expression and requires the combined activities of E2A (show TCF3 Proteins) and HEB
These results showed a new set of interactions between HEB, Notch1 (show NOTCH1 Proteins), and GATA3 (show GATA3 Proteins) that regulate the T-cell fate choice in developing thymocytes.
Developmental progression of fetal HEB(-/-) precursors to the pre-T-cell stage is restored by HEBAlt.
HEB is a specific and essential factor in T-cell development and in the generation of the iNKT cell lineage.
the dosage of HEB determines pT alpha (show PTCRA Proteins) 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