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SETMAR encodes a fusion protein that contains an N-terminal histone-lysine N-methyltransferase domain and a C-terminal mariner transposase domain. Additionally we are shipping SETMAR Proteins (15) and SETMAR Kits (4) and many more products for this protein.
Showing 10 out of 36 products:
Cow (Bovine) Polyclonal SETMAR Primary Antibody for WB - ABIN374285
Robertson, Zumpano: Molecular evolution of an ancient mariner transposon, Hsmar1, in the human genome. in Gene 1998
The SET domain is needed for the 5' end of ss-overhang cleavage with fork and non-fork DNA without affecting the Metnase-DNA interaction. This domain has a positive role in restart of replication fork and the 5' end of ss-overhang cleavage.
methylation of snRNP70 (show SNRNP70 Antibodies) by SETMAR regulates constitutive and/or alternative splicing
Metnase may possess an important role in DNA repair, topoisomerase II (show TOP2 Antibodies) function, and the maintenance of stemness during colon cancer development.
293 T transfected with Metnase revealed a large number of rescued plasmids.
found known and novel SETMAR splice variants to be significantly increased in acute myeloid leukemia (show BCL11A Antibodies)
a single mutation DDN(610) --> DDD (show KRT5 Antibodies)(610), which restores the ancestral catalytic site, results in loss of function in Metnase
phosphorylation of Metnase S495 differentiates between these two functions, enhancing DSB repair and repressing replication fork restart.
Data show that DBN1 (show DBN1 Antibodies), SETMAR and HIG2 (show HILPDA Antibodies) are direct transcriptional targets of the SOX11 (show SOX11 Antibodies) protein.
DNA repair protein (show ATRIP Antibodies) Metnase (also SETMAR), which has a SET histone methylase domain, localized to an induced DSB and directly mediated the formation of H3K36me2 near the induced DSB
results establish Metnase as a key factor that promotes restart of stalled replication forks, and implicate Metnase in the repair of collapsed forks.
The suppression of Notch-1 (show NOTCH1 Antibodies) led to increased expression of Oct4 (show POU5F1 Antibodies) and Sox2 (show SOX2 Antibodies), but in decreased gene expression of cMET, Setmar and CD44 (show CD44 Antibodies).
Metnase may have been selected for because it has a function opposing transposases and may thus play a key role in suppressing translocations that underlie oncogenicity.
This gene encodes a fusion protein that contains an N-terminal histone-lysine N-methyltransferase domain and a C-terminal mariner transposase domain. The encoded protein binds DNA and functions in DNA repair activities including non-homologous end joining and double strand break repair. The SET domain portion of this protein specifically methylates histone H3 lysines 4 and 36. This gene exists as a fusion gene only in anthropoid primates, other organisms lack mariner transposase domain. Alternate splicing results in multiple transcript variants.
SET domain and mariner transposase fusion gene
, histone-lysine N-methyltransferase SETMAR
, SET domain and mariner transposase fusion
, SET domain without mariner transposase fusion
, histone-lysine N-methyltransferase SETMAR-like
, SET domain and mariner transposase fusion gene-containing protein
, SET domain and mariner transposase fusion gene-containing protein homolog
, epidermal tumor expressed transcript 2