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Histone demethylase that specifically demethylates 'Lys- 27' of histone H3, thereby playing a central role in histone code. Additionally we are shipping Kdm6b Antibodies (95) and and many more products for this protein.
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Data show that Spi1 (show SPI1 ELISA Kits) is a downstream target of histone demethylase Jmjd3 (Jmjd3) during myelopoiesis.
loss of both kdm6ba and kdm6bb shows Kdm6b proteins share redundant and pleiotropic roles in organogenesis without impacting initial cell fate specification.
Data demonstrate that histone modifications silence promoters of numerous genes involved in zebrafish caudal fin regeneration, and that Kdm6b.1 may be the histone demethylase required during regeneration.
Our data show that chemical inhibition of the H3K27me3 demethylases Jmjd3/Utx blunts Neurogenin3 (show NEUROG3 ELISA Kits)-dependent gene activation in vitro. Conversely, inhibition of the H3K27me3 methyltransferase Ezh2 (show EZH2 ELISA Kits) enhances both the transactivation ability of Neurogenin3 (show NEUROG3 ELISA Kits) in cultured cells and the formation of insulin (show INS ELISA Kits)-producing cells during directed differentiation from pluripotent cells
Study indicates sequential chromatin events and identifies a crucial role for Jmjd3 in regulating the efficiency of the transition from Ngn3 (show NEUROG3 ELISA Kits)-low to Ngn3 (show NEUROG3 ELISA Kits)-high cells.
When JMJD3 levels were decreased by RNA interference, the embryo development rate and quality were improved, but the knockdown of UTX produced the opposite results.
binding of SMAD2 (show SMAD2 ELISA Kits)/3, the intracellular effectors of activin signaling, was significantly enriched at the Pmepa1 (show PMEPA1 ELISA Kits) gene, which encodes a negative feedback regulator of TGF-beta (show TGFB1 ELISA Kits) signaling in cancer cells, and at the Kdm6b gene, which encodes an epigenetic regulator promoting transcriptional plasticity.
Results identified Kdm6b as a novel regulator of the pro-fibrotic signature of peritoneal foam cells.
These results suggest that the demethylase activity of Jmjd3, but not that of Utx, affects mouse axial patterning in concert with alterations in Hox (show MSH2 ELISA Kits) gene expression.
Direct genetic and molecular evidence that JMJD3 is a key mediator for the kisspeptin-estrogen feedback loop.
Knockdown of Kdm6b in chondrocytes leads to abnormal cartilage development and accelerated osteoarthritis progression via inhibition of the anabolic metabolism of chondrocytes. The number of Kdm6b-positive chondrocytes was lower in osteoarthritis cartilage samples.
Preliminary evidence suggests a role of JMJD3 in removal of H3K27me3 mark from promoters of hepatic transcription factors, thus activating epigenetically poised hepatic genes in bone marrow progenitor cells prior to partial nuclear reprogramming.
Study provides evidence that miR (show MLXIP ELISA Kits)-148a-3p reciprocally regulates adipocyte and osteoblast differentiation through directly targeting Kdm6b.
The KDM6B inhibitor GSK-J4 perturbed the PMA-mediated differentiation of THP-1 (show GLI2 ELISA Kits) cells. The AURKA (show AURKA ELISA Kits) inhibitor alisertib accelerates the expression of the H3K27 demethylase KDM6B, dissociating AURKA (show AURKA ELISA Kits) and YY1 (show YY1 ELISA Kits) from the KDM6B promoter region and inducing differentiation.
The interaction of methyltransferase EZH2 (show EZH2 ELISA Kits) or demethylase JMJD3 on RGMA (show RGMA ELISA Kits), RARb2, AR, PGR (show PGR ELISA Kits), and ERa genes in the progression and aggressiveness of prostate cancer.
We demonstrate that extraskeletal osteosarcoma (ESOS) may include at least two small subsets: an MDM2 (show MDM2 ELISA Kits)-amplified deep soft-tissue ESOS and an H3K27me3-deficient organ-based ESOS
Our results demonstrate that in the early stage of sepsis, JMJD3 contributes to high levels of neutrophil mPR3 (show PRTN3 ELISA Kits) expression and thereby to the production of the inflammatory cytokine IL-1beta (show IL1B ELISA Kits)
Computational methods identifyied H3(17-33)-derived peptides with improved binding affinity that would allow co-crystallization with the KDM6B catalytic core. A co-crystallized H3(17-33)A21M peptide had interactions between the KDM6B zinc binding domain and the H3(17-23) region. KDM6B uses the zinc binding domain to achieve H3K27me3/me2 specificity. A 1564 His-to-Gln substitution explains its higher affinity than KDM6A.
Taken together, the authors propose that the miR (show MLXIP ELISA Kits)-939-Jmjd3 axis perturbs the accessibility of hepatitis B virus enhancer II/core promoter (En II) promoter to essential nuclear factors (C/EBPalpha (show CEBPA ELISA Kits) and SWI/SNF (show SNRPA ELISA Kits) complex) therefore leading to compromised viral RNA synthesis and hence restricted viral multiplication.
These results demonstrated that histone demethylase JMJD3 regulates CD11a (show ITGAL ELISA Kits) expression in lupus T cells by affecting the H3K27me3 levels in the ITGAL (CD11a (show ITGAL ELISA Kits)) promoter region, and JMJD3 might thereby serve as a potential therapeutic target for SLE.
In this study, we showed that aberrantly upregulated JMJD3 exerts an anti-apoptotic effect in diffuse large B-cell lymphoma
Our study therefore delineates KDM6B function that links NF-kappaB (show NFKB1 ELISA Kits) and MAPK (show MAPK1 ELISA Kits) signaling pathway mediating MM cell growth and survival, and validates KDM6B as a novel therapeutic target in MM.
Histone demethylase that specifically demethylates 'Lys- 27' of histone H3, thereby playing a central role in histone code. Demethylates trimethylated and dimethylated H3 'Lys-27'. Plays a central role in regulation of posterior development, by regulating HOX gene expression. Involved in inflammatory response by participating in macrophage differentiation in case of inflammation by regulating gene expression and macrophage differentiation.
jumonji domain containing 3
, lysine (K)-specific demethylase 6B
, jumonji domain containing 3, histone lysine demethylase
, lysine-specific demethylase 6B-like
, jmjC domain-containing protein 3
, jumonji domain-containing protein 3
, lysine-specific demethylase 6B
, lysine demethylase 6B
, jumonji domain-containing 3