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SUV420H1 encodes a protein that contains a SET domain. De plus, nous expédions Suppressor of Variegation 4-20 Homolog 1 (Drosophila) Protéines (5) et beaucoup plus de produits pour cette protéine.
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Dog (Canine) Polyclonal SUV420H1 Primary Antibody pour IHC, WB - ABIN2775877
Twells, Metzker, Brown, Cox, Garey, Hammond, Hey, Levy, Nakagawa, Philips, Todd, Hess: The sequence and gene characterization of a 400-kb candidate region for IDDM4 on chromosome 11q13. dans Genomics 2001
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Cow (Bovine) Polyclonal SUV420H1 Primary Antibody pour WB - ABIN2775991
Ewing, Chu, Elisma, Li, Taylor, Climie, McBroom-Cerajewski, Robinson, OConnor, Li, Taylor, Dharsee, Ho, Heilbut, Moore, Zhang, Ornatsky, Bukhman, Ethier, Sheng, Vasilescu, Abu-Farha, Lambert, Duewel et al.: Large-scale mapping of human protein-protein interactions by mass spectrometry. ... dans Molecular systems biology 2007
epsilon-globin expression is regulated by SUV4-20h1.
Altogether, these results reveal Suv4-20h-mediated histone H4K20 tri-methylation as a critical determinant in the selection of active replication initiation sites in heterochromatin regions of mammalian genomes.
overexpression of SUV420H1 may result in activation of the ERK signaling pathway
Strong statistical evidence for a causal role of SUV420H1 in autism.
This study suggests a novel role of FRG1 as epigenetic regulator of muscle differentiation and indicates that Suv4-20h1 has a gene-specific function in myogenesis.
The crystal structure of SUV420H1 was used to characterize substrate selectivity and product specificity.
SUV420H1 and SUV420H2 isoforms have different in their cellular localization and effects on myogenic differentiation
The data indicate that Suv4-20 generates nearly ubiquitous dimethylation that facilitates the DNA damage response and selective trimethylation that is involved in heterochromatin formation.[Suv4-20]
dissect the GRIP1:Suv4-20h1 interaction in vitro and in vivo and examine its potential involvement in hormone-dependent transcriptional regulation by GR
Suv4-20h1/h2 are mostly absent in mouse embryos before implantation, underscoring a rapid decrease of H4K20me3 from the two-cell stage onward
Suv4-20h1, an H4K20 dimethyltransferase, controls Skeletal muscle stem cell quiescence by promoting formation of facultative heterochromatin.
Data suggest that Suv4-20h1/Suv4-20h2 activity is required for fidelity of chromosome distribution during meiosis in oocyte; Suv4-20h1/Suv4-20h2 appear to control histone 4 methylation, centromere structure, and oocyte maturation/oogenesis.
murine Suv4-20h1/h2 double-knockout embryonic stem (DKO ES) cells exhibit increased Oct4 protein levels before and during EB formation, and reveal a compromised and biased capacity for in vitro differentiation, when compared to normal ES cells
Abrogation of Suv4-20h enzymes and loss of heterochromatic mark H4K20me3 at telomeric heterochromatin facilitates telomere reprogramming and provides an increased tumorigenic potential to induced pluripotent stem cells.
There is a novel role for histone lysine methylation in controlling telomere recombination.
This gene encodes a protein that contains a SET domain. SET domains appear to be protein-protein interaction domains that mediate interactions with a family of proteins that display similarity with dual-specificity phosphatases (dsPTPases). The function of this gene has not been determined. Two alternatively spliced transcript variants have been found for this gene.
suppressor of variegation 4-20 homolog 1 (Drosophila)
, histone-lysine N-methyltransferase SUV420H1
, su(var)4-20 homolog 1
, suppressor of variegation 4-20 protein-like 1
, histone-lysine N-methyltransferase SUV420H1-like
, histone-lysine N-methyltransferase SUV420H1-A
, su(var)4-20 homolog 1-A
, suppressor of variegation 4-20 homolog 1-A
, suv4-20 h1
, lysine N-methyltransferase 5B