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SUV420H2 and the related enzyme SUV420H1 (MIM 610881) function as histone methyltransferases that specifically trimethylate nucleosomal histone H4 (see MIM 602822) on lysine-20 (K20) (Schotta et al., 2004. Additionally we are shipping Suppressor of Variegation 4-20 Homolog 2 (Drosophila) Proteins (7) and many more products for this protein.
Showing 10 out of 21 products:
Mouse (Murine) Polyclonal SUV420H2 Primary Antibody for WB - ABIN656011
Yang, Pesavento, Starnes, Cryderman, Wallrath, Kelleher, Mizzen: Preferential dimethylation of histone H4 lysine 20 by Suv4-20. in The Journal of biological chemistry 2008
Human Polyclonal SUV420H2 Primary Antibody for EIA, WB - ABIN453403
Tryndyak, Kovalchuk, Pogribny: Loss of DNA methylation and histone H4 lysine 20 trimethylation in human breast cancer cells is associated with aberrant expression of DNA methyltransferase 1, Suv4-20h2 histone methyltransferase and methyl-binding proteins. in Cancer biology & therapy 2006
Human Polyclonal SUV420H2 Primary Antibody for FACS, WB - ABIN390405
Souza, Völkel, Trinel, Vandamme, Rosnoblet, Héliot, Angrand: The histone methyltransferase SUV420H2 and Heterochromatin Proteins HP1 interact but show different dynamic behaviours. in BMC cell biology 2009
Upregulation of long non-coding RNA PAPAS (show PSTPIP1 Antibodies) in response to hypoosmotic stress does not increase H4K20me3 because of Nedd4 (show NEDD4 Antibodies)-dependent ubiquitinylation and proteasomal degradation of Suv4-20h2.
One of the most downregulated genes in response to SUV420H2 expression was the Src (show SRC Antibodies) substrate, tensin-3 (show TNS3 Antibodies), a focal adhesion protein that contributes to cancer cell migration.
The crystal structure of SUV420H2 was used to characterize substrate selectivity and product specificity.
SUV420H1 (show SUV420H1 Antibodies) and SUV420H2 isoforms have different in their cellular localization and effects on myogenic differentiation
data indicate that H4K20me3 invokes gene repression by antagonizing hMOF (show KAT8 Antibodies)-mediated H4K16Ac
The decrease in trimethylation of lysine 20 of histone H4 in breast cancer cells was accompanied by diminished expression of Suv4-20h2 histone methyltransferase.
Upregulation of long non-coding RNA PAPAS (show PSTPIP1 Antibodies) in response to hypoosmotic stress does not increase H4K20me3 because of Nedd4-dependent ubiquitinylation and proteasomal degradation of Suv4-20h2.
Results uncover a lncRNA-mediated mechanism that guides Suv4-20h2 to specific genomic loci to establish a more compact chromatin structure in growth-arrested cells.
Data suggest that Suv4-20h1 (show SUV420H1 Antibodies)/Suv4-20h2 activity is required for fidelity of chromosome distribution during meiosis in oocyte; Suv4-20h1 (show SUV420H1 Antibodies)/Suv4-20h2 appear to control histone 4 methylation, centromere structure, and oocyte maturation/oogenesis.
Suv4-20h2 is involved in the initial loading or maintenance of cohesion subunits
SUV420H2 and the related enzyme SUV420H1 (MIM 610881) function as histone methyltransferases that specifically trimethylate nucleosomal histone H4 (see MIM 602822) on lysine-20 (K20) (Schotta et al., 2004
suppressor of variegation 4-20 homolog 2 (Drosophila)
, suppressor of variegation 4-20 protein-like 2
, histone-lysine N-methyltransferase SUV420H2-like
, histone-lysine N-methyltransferase SUV420H2
, su(var)4-20 homolog 2
, lysine N-methyltransferase 5C