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Members of the ten-eleven translocation (TET) gene family, including TET3, play a role in the DNA methylation process (Langemeijer et al., 2009 [PubMed 19923888]).[supplied by OMIM, Nov 2010].. Additionally we are shipping and many more products for this protein.
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Mouse (Murine) Polyclonal TET3 Primary Antibody for WB - ABIN2668513
Otani, Kimura, Sharif, Endo, Mishima, Kawakami, Koseki, Shirakawa, Suetake, Tajima: Cell cycle-dependent turnover of 5-hydroxymethyl cytosine in mouse embryonic stem cells. in PLoS ONE 2013
Human Polyclonal TET3 Primary Antibody for IHC, IHC (p) - ABIN4358587
Ni, Dansranjavin, Rogenhofer, Oeztuerk, Deuker, Bergmann, Schuppe, Wagenlehner, Weidner, Steger, Schagdarsurengin: TET enzymes are successively expressed during human spermatogenesis and their expression level is pivotal for male fertility. in Human reproduction (Oxford, England) 2016
TET1 (show TET1 Antibodies), TET2 (show TET2 Antibodies), and TET3 genes are downregulated in endometriosis.
Results revealed that TET3 acted as a suppressor of ovarian cancer by demethylating miR (show MLXIP Antibodies)-30d precursor gene promoter to block TGF-beta1 (show TGFB1 Antibodies)-induced epithelial-mesenchymal transition.
TET3 expression inhibits glioblastoma tumorigenesis and self-renewal in glioblastoma stem cells.
levels of TET3 and TDG (show TDG Antibodies) mRNAs were independent prognostic factors for early breast cancer patients who received anthracycline chemotherapy
Hypoxia deregulates TET3. TET1 (show TET1 Antibodies)/3 levels were associated with tumor hypoxia, tumor malignancy, and poor prognosis in breast cancer patients. Coordinate functions of TET1 (show TET1 Antibodies) and TET3 were needed to activate TNFalpha (show TNF Antibodies)-p38-MAPK (show MAPK14 Antibodies) signaling in hypoxia.
In hepatic stellate cells, cell proliferation rise significantly and cell apoptosis reduce obviously after knockdown of TET3.
GABRA3 (show GABRA3 Antibodies) also carries a microRNA (miR (show MLXIP Antibodies)-767) with predicted target sites in TET1 (show TET1 Antibodies) and TET3, two members of the ten-eleven-translocation family of tumor suppressor genes, involved in the conversion of 5-methylcytosines to 5-hydroxymethylcytosines in DNA.
TET1 (show TET1 Antibodies), TET2 (show TET2 Antibodies), and TET3 are highly phosphorylated.
TET1 (show TET1 Antibodies) depletion yields widespread reduction of 5hmC, while depletion of TET2 (show TET2 Antibodies) and TET3 reduces 5hmC at a subset of TET1 (show TET1 Antibodies) targets suggesting functional co-dependence.
OGT (show OGT Antibodies) catalyzes the O-GlcNAcylation of TET3, promotes TET3 nuclear export, and, consequently, inhibits the formation of 5-hydroxymethylcytosine catalyzed by TET3.
The CXXC domain of Tet3 has the capacity to bind to unmethylated and carboxylated cytosines at CpG sequences and a very restricted genomic localization pattern with a preference for transcription start sites.
Genetic ablation of TET3 in oocytes had no significant effect on oocyte development.
the stability of Foxp3 (show FOXP3 Antibodies) expression is markedly compromised in T reg (show KCNH2 Antibodies) cells from Tet2 (show TET2 Antibodies)/Tet3 double-deficient mice.
The DNA demethylation marks are dynamically regulated in both in vivo and in vitro aging conditions, which are associated with Tet3 over-expression and Tdg (show TDG Antibodies) repression.
Knockdown of Tet1 (show TET1 Antibodies) and Tet3 by RNAi in ex vivo cerebellar slice cultures inhibits dendritic arborization of developing cerebellar granule cells, a critical step in circuit formation
This paper demonstrates a Tet3-dependent mechanism underlying the dexamethasone-induced epigenetic reprogramming leading to heritable alterations of a fundamental player in cortical development.
We propose a mechanism for transcriptional activation in neurons that involves REST-guided targeting of TET3 to the DNA for directed 5hmC generation and NSD3 (show WHSC1L1 Antibodies)-mediated H3K36 trimethylation
results not only reveal a link between miRNAs, TET, and DNA demethylation but also demonstrate critical roles for miR (show MLXIP Antibodies)-15b and TET3 in maintaining the NPC (show NPC1 Antibodies) pool during early neocortical development.
Embryos lacking Tet1 (show TET1 Antibodies) and Tet3 (Tet1 (show TET1 Antibodies)/3 DKO) displayed a strong loss of 5-hydroxymethylcytosine (5hmC) and a concurrent increase in 5-methylcytosine (5mC) at the eight-cell stage.
Tet3 is important for neural progenitor cell maintenance and terminal differentiation of neurons.
Members of the ten-eleven translocation (TET) gene family, including TET3, play a role in the DNA methylation process (Langemeijer et al., 2009
probable methylcytosine dioxygenase TET3
, tet oncogene family member 3
, methylcytosine dioxygenase TET3