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The protein encoded by EHMT1 is a histone methyltransferase that is part of the E2F6 complex, which represses transcription. De plus, nous expédions EHMT1 Protéines (4) et EHMT1 Kits (2) et beaucoup plus de produits pour cette protéine.
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Human Polyclonal EHMT1 Primary Antibody pour WB - ABIN387855
Ogawa, Ishiguro, Gaubatz, Livingston, Nakatani: A complex with chromatin modifiers that occupies E2F- and Myc-responsive genes in G0 cells. dans Science (New York, N.Y.) 2002
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Human Polyclonal EHMT1 Primary Antibody pour EIA, WB - ABIN4620519
Ota, Suzuki, Nishikawa, Otsuki, Sugiyama, Irie, Wakamatsu, Hayashi, Sato, Nagai, Kimura, Makita, Sekine, Obayashi, Nishi, Shibahara, Tanaka, Ishii, Yamamoto, Saito, Kawai, Isono, Nakamura, Nagahari et al.: Complete sequencing and characterization of 21,243 full-length human cDNAs. ... dans Nature genetics 2003
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The stress-induced Brg1 (Montrer SMARCA4 Anticorps)-G9a (Montrer EHMT2 Anticorps)/GLP (Montrer GOLGA6A Anticorps)-Dnmt3 interactions and sequence of repressive chromatin assembly on Myh6 (Montrer MYH6 Anticorps) promoter illustrates a molecular mechanism by which the heart epigenetically responds to environmental signals.
data provide genetic and pharmacologic evidence that EHMT1 and EHMT2 (Montrer EHMT2 Anticorps) are epigenetic regulators involved in gamma-globin repression and represent a novel therapeutic target for SCD (Montrer SCD Anticorps).
histone methyltransferase activities of GLP (Montrer GOLGA6A Anticorps) and G9a (Montrer EHMT2 Anticorps) are stimulated by neighboring nucleosomes that are premethylated at H3K9
Prdm16 (Montrer PRDM16 Anticorps) was required in young mice to suppress the expression of white-fat-selective genes in BAT (Montrer BAAT Anticorps) through recruitment of the histone methyltransferase Ehmt1.
G9a (Montrer EHMT2 Anticorps) and GLP (Montrer GOLGA6A Anticorps) have an essential role in normal morphogenesis of the atrioventricular septum through regulation of the size of the atrioventricular cushion.
Reduced Euchromatin histone methyltransferase 1 (Montrer DNMT1 Anticorps) causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice.
EHMT1 is an essential BAT (Montrer BAAT Anticorps)-enriched lysine methyltransferase in the PRDM16 (Montrer PRDM16 Anticorps) transcriptional complex and controls brown adipose cell fate
These data demonstrate that Ehmt1 haploinsufficiency in mice leads to learning deficits and synaptic dysfunction, providing a possible mechanism for the ID phenotype in patients with Kleefstra syndrome
Metallothionein 1 (Montrer MT1 Anticorps) h tumour suppressor activity in prostate cancer is mediated by euchromatin methyltransferase 1 (Montrer DNMT1 Anticorps).
EHMT1 protein binds to nuclear factor-kappaB p50 (Montrer NFKB1 Anticorps) and represses gene expression.
we find an estrogen receptor (Montrer ESR1 Anticorps)-independent synthetic lethal interaction between a GATA3 (Montrer GATA3 Anticorps) frameshift mutant with an extended C-terminus and the histone methyltransferases G9A (Montrer EHMT2 Anticorps) and GLP (Montrer RCBTB1 Anticorps), indicating perturbed epigenetic regulation
Selective degradation of the mutant EHMT1 mRNA leads to Kleefstra syndrome.
G9a (Montrer EHMT2 Anticorps) and GLP (Montrer RCBTB1 Anticorps) are required for stable maintenance of imprinted DNA methylation (Montrer HELLS Anticorps) in embryonic stem cells.
the clinical picture we found in Norwegian patients with Kleefstra syndrome is similar to the findings described in the literature. An interesting point is that in the literature >85% of the patients have a deletion of 9q34.3 and the remaining have a mutation in the EHMT1 gene, whereas in this study we found 50% with a deletion, and 50% with a mutation.
Data indicate zinc finger proteins ZNF644 (Montrer ZNF644 Anticorps) and WIZ (Montrer ZNF803 Anticorps) as two core subunits in the histone-lysine N-methyltransferase G9a (Montrer EHMT2 Anticorps)/GLP (Montrer RCBTB1 Anticorps) complex, and interact with the transcription activation domain of G9a (Montrer EHMT2 Anticorps) and GLP (Montrer RCBTB1 Anticorps).
data provide genetic and pharmacologic evidence that EHMT1 and EHMT2 (Montrer EHMT2 Anticorps) are epigenetic regulators involved in gamma-globin (Montrer HBG1 Anticorps) repression and represent a novel therapeutic target for SCD (Montrer SCD Anticorps).
The expression level of EHMT1 and EHMT2 (Montrer EHMT2 Anticorps) inversely correlates with the type I interferon (Montrer IFNA Anticorps) responsiveness in chronic myeloid leukemia (Montrer BCL11A Anticorps) cell lines.
The current knowledge on the mechanisms of action and function of EHMT1, with particular emphasis on their interplay in the regulation of chromatin states and biological processes.
Haploinsufficiency of EHMT1 caused by either microdeletions at 9q34.3 or intragenic mutations are associated with Kleefstra syndrome.
PRC2 and G9a (Montrer EHMT2 Anticorps)/GLP (Montrer RCBTB1 Anticorps) interact physically and functionally.
The protein encoded by this gene is a histone methyltransferase that is part of the E2F6 complex, which represses transcription. The encoded protein methylates the Lys-9 position of histone H3, which tags it for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome). Two transcript variants encoding different isoforms have been found for this gene.
euchromatic histone methyltransferase 1
, histone-lysine N-methyltransferase, H3 lysine-9 specific 5
, euchromatic histone-lysine N-methyltransferase 1
, histone-lysine N-methyltransferase EHMT1
, histone-lysine N-methyltransferase, H3 lysine-9 specific 5-like
, G9a-like protein 1
, lysine N-methyltransferase 1D
, G9a like protein
, H3-K9-HMTase 5
, histone H3-K9 methyltransferase 5