Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Alle Spezies anzeigen
Weitere Synonyme anzeigen
Wählen Sie die Spezies und Applikation aus
anti-Human Exonuclease 1 Antikörper:
anti-Mouse (Murine) Exonuclease 1 Antikörper:
anti-Rat (Rattus) Exonuclease 1 Antikörper:
Sie gelangen zu unserer vorgefilterten Suche.
Human Polyclonal Exonuclease 1 Primary Antibody für ChIP, ICC - ABIN4309747
Peterson, Li, Chait, Gottesman, Baer, Gautier: Cdk1 uncouples CtIP-dependent resection and Rad51 filament formation during M-phase double-strand break repair. in The Journal of cell biology 2011
Show all 3 Pubmed References
Human Polyclonal Exonuclease 1 Primary Antibody für IHC - ABIN966108
Qiu, Qian, Chen, Guan, Shen: Human exonuclease 1 functionally complements its yeast homologues in DNA recombination, RNA primer removal, and mutation avoidance. in The Journal of biological chemistry 1999
Show all 15 Pubmed References
Human Polyclonal Exonuclease 1 Primary Antibody für ELISA, WB - ABIN408657
Kim, Roh, Yoon, Kim, Park: MLH3 and EXO1 alterations in familial colorectal cancer patients not fulfilling Amsterdam criteria. in Cancer genetics and cytogenetics 2007
has exonuclease properties that are similar to the human WRN protein
The finding that a threading mechanism like that used by hFEN1 is also used by hEXO1 unifies the mode of operation for members of the 5'-nuclease superfamily that act on discontinuous substrates. As with hFEN1, intrinsic disorder of the arch region of the protein may explain how flaps can be threaded without a need for a coupled energy source.
These findings indicate that the coupling of EXO1 activation with its eventual degradation is a timing mechanism that limits the extent of DNA end resection for accurate DNA repair.
Mutations in the human EXO1 gene correlate with increased susceptibility to some cancers. This review summarizes recent studies on the enzymatic functions and biological roles of EXO1, its possible protective role against cancer and aging, and regulation of EXO1 by posttranslational modification. [review]
These results suggest that Metnase (zeige SETMAR Antikörper) enhances Exo1-mediated exonuclease activity on the lagging strand DNA by facilitating Exo1 loading onto a single strand gap at the stalled replication fork.
we present evidence that the inherited EXO1 polymorphism rs9350 may have a substantial influence on prostate cancer risk in Chinese people. We believe that the rs9350 could be a useful biomarker for assessing predisposition for and early diagnosis of prostate cancer.
study concludes that Exo1 gene polymorphism Lys589Glu may be associated with an increased risk of colorectal cancer in the Polish population
Mutations within the EXO1 gene are not associated with premature ovarian failure in Han Chinese women.
EXO1 is more active on DNA at temperatures below 37 degrees C and this manifests as an increase in nuclease (zeige DCLRE1C Antikörper) activity.EXO1 preferentially cleaves one nucleotide inwards in a double stranded region of forked and nicked DNA flap (zeige ALOX5AP Antikörper) substrates.
CRL4(Wdr70) regulates H2B monoubiquitination and facilitates Exo1-dependent DNA repair resection.
MSH2 (zeige MSH2 Antikörper), MSH6 (zeige MSH6 Antikörper), and EXO1 genes were overexpressed in gastroesophageal cancers.
like canonical DNA mismatch-repair proteins, EXO1 can restrain aberrant homologous recombination events between diverged sequence elements in the genome.
The results establish a key role for EXO1 in modulating the severity of hypomorphic MRE11 (zeige MRE11A Antikörper) complex mutations.
Exo1-mediated HR is dispensable for stem cell function in quiescent HSC (zeige FUT1 Antikörper), whereas it is essential to HSC (zeige FUT1 Antikörper) response to DNA damage processing after cell cycle entry, and its loss is not compensated by intact NHEJ
In contrast to Exo1(null/null) mice, Exo1(E109K/E109K) knockin mice retain mismatch repair activity and display normal class switch recombination and meiosis.
RNAi-mediated EXO1 knockdown in mouse fibroblasts directly results in an alkylation-tolerant phenotype.
Exo1 contributes to the metabolism of DNA ends during DNA double-strand breaks repair in B lymphocytes.
Study documents the combinatorial action of Apollo (zeige DCLRE1B Antikörper), POT1b, CST (zeige CORT Antikörper), and the 5' exonuclease Exo1 in postreplicative telomere end processing in mouse cells, clarifying the mechanism by which the telomeric 3' overhang is generated and modulated.
EXO1 can convert DNA nicks and point mutations into double-stranded DNA breaks for both core nonhomologous end-joining factors and alternative end-joining pathways of class-switch recombination.
Apc (zeige APC Antikörper)(1638N) Exo1 Fen1 (zeige FEN1 Antikörper) mice survive longer (18 months)
EXO1 contributes to DNA damage signal induction in mammalian cells, and deletion of Exo1 can prolong survival in the context of telomere dysfunction.
This gene encodes a protein with 5' to 3' exonuclease activity as well as an RNase H activity. It is similar to the Saccharomyces cerevisiae protein Exo1 which interacts with Msh2 and which is involved in mismatch repair and recombination. Alternative splicing of this gene results in three transcript variants encoding two different isoforms.
, exonuclease I Exo1
, RNA exonuclease
, exonuclease 1
, rad2 nuclease family member, homolog of S. cerevisiae exonuclease 1
, exonuclease I
, exonuclease ExoI