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Chicken Polyclonal MRE11A Primary Antibody für ChIP, FACS - ABIN151076
Wang, Cortez, Yazdi, Neff, Elledge, Qin: BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures. in Genes & development 2000
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Human Monoclonal MRE11A Primary Antibody für ELISA, Func - ABIN151920
Carney, Maser, Olivares, Davis, Le Beau, Yates, Hays, Morgan, Petrini: The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response. in Cell 1998
Show all 23 Pubmed References
Human Monoclonal MRE11A Primary Antibody für IF, WB - ABIN968498
Haber: The many interfaces of Mre11. in Cell 1998
Show all 3 Pubmed References
Human Polyclonal MRE11A Primary Antibody für IF (p), IHC (p) - ABIN747293
Yuan, Han, Cong, Ge, Ma, Dai, Li, Bi: Docetaxel-loaded solid lipid nanoparticles suppress breast cancer cells growth with reduced myelosuppression toxicity. in International journal of nanomedicine 2014
Human Polyclonal MRE11A Primary Antibody für IHC (p), WB - ABIN4335394
Salvati, Scarsella, Porru, Rizzo, Iachettini, Tentori, Graziani, DIncalci, Stevens, Orlandi, Passeri, Gilson, Zupi, Leonetti, Biroccio: PARP1 is activated at telomeres upon G4 stabilization: possible target for telomere-based therapy. in Oncogene 2010
the essential role of Nbs1 (zeige NBN Antikörper) is via its interaction with Mre11 and that most of the Nbs1 (zeige NBN Antikörper) protein is dispensable for Mre11 complex functions and suggest that Mre11 and Rad50 (zeige RAD50 Antikörper) directly activate ATM (zeige ATM Antikörper).
Low MRE11 expression is associated with B-cell lymphomas.
cyclin A2 (zeige CCNA2 Antikörper) controlled Mre11 abundance through a C-terminal RNA binding domain that selectively and directly binds Mre11 transcripts to mediate polysome loading and translation.
MRE11 complex influences the elimination of oocytes with unrepaired meiotic double-strand breaks post-natally, in addition to its previously described role in double-strand break repair and homologous synapsis during female meiosis.
Inhibiting MRE11 by mirin during meiotic maturation results in anaphase bridges and also increases the number of gammaH2AX (zeige H2AFX Antikörper) foci in metaphase II. Compromised DNA integrity in mirin-treated oocytes indicates a role for MRE11 in chromosome integrity during meiotic maturation.
The authors demonstrate that ATM (zeige ATM Antikörper) can be activated by DNA double-strand breaks in the absence of the Mre11-Rad50 (zeige RAD50 Antikörper)-NBS1 (zeige NBN Antikörper) (MRN) sensor complex.
TRIP13 (zeige TRIP13 Antikörper)-deficient spermatocytes also progress to an H1t (zeige HIST1H1T Antikörper)-positive stage if ATM (zeige ATM Antikörper) activity is attenuated by hypomorphic mutations in Mre11 or Nbs1 (zeige NBN Antikörper) or by elimination of the ATM (zeige ATM Antikörper)-effector kinase CHK2 (zeige CHEK2 Antikörper)
Impairment of Mre11 complex functions promotes the progression of mammary hyperplasias into invasive and metastatic breast cancers
results suggest that the MRE11-RAD50 (zeige RAD50 Antikörper) complex plays important roles in recognition of dsDNA and initiation of STING-dependent signaling, in addition to its role in DNA-damage responses
The critical role of the MRE11 GAR motif in DSB repair is a mechanistic link between post-translational modifications at the MRE11 GAR motif and DSB processing, as well as the ATR (zeige ATR Antikörper)/CHK1 (zeige CHEK1 Antikörper) checkpoint signaling.
MRE11A gene polymorphism is associated with colorectal cancer.
Low MRE11 expression is associated with low-grade epithelial ovarian cancer.
although recruitment of the MRE11-RAD50 (zeige RAD50 Antikörper)-NBS1 (zeige NBN Antikörper) (MRN) DSB-sensing complex to viral genomes and activation of the ATM (zeige ATM Antikörper) kinase can promote KSHV replication, proteins involved in nonhomologous end joining (NHEJ) repair restrict amplification of viral DNA.
Mre11-Rad50 (zeige RAD50 Antikörper)-Nbs1 (zeige NBN Antikörper) complex initiates DNA double strand break repair.
we show that Plk1 (zeige PLK1 Antikörper) phosphorylates Mre11 at S649 during G2 DNA damage recovery and Mre11 phosphorylation at S649/S689 drives premature checkpoint termination and reduced DNA repair
In the absence of RAD51 (zeige RAD51 Antikörper), the unprotected newly replicated genome is degraded by the exonuclease (zeige EXO1 Antikörper) activity of MRE11, and the fragmented nascent DNA accumulates in the cytosol, initiating an innate immune response.
Both the genome instability and cell death of MRE11-null and MRE11-mutated H129N cells are significantly reversed by overexpression of Tdp2 (zeige TDP2 Antikörper), an enzyme that eliminates covalent Top2 (zeige TOP2A Antikörper) conjugates; thus, the essential role of Mre11 nuclease (zeige DCLRE1C Antikörper) activity is likely to remove the DNA lesions.
The results illuminate the important role of Nbs1 (zeige NBN Antikörper) and CtIP (zeige RBBP8 Antikörper) in determining the substrates and consequences of human Mre11/Rad50 (zeige RAD50 Antikörper) nuclease (zeige DCLRE1C Antikörper) activities on protein-DNA lesions.
Cdk-dependent phosphorylation of TRF1 on threonine 371 promotes TRF1 to interact with APBs in S and G2 phases independently of its binding to telomeric DNA. We have demonstrated that the interaction of (pT371)TRF1 with APBs is dependent upon ATM and homologous-recombination-promoting factors such as Mre11 and BRCA1.
Ataxia-telangiectasia-like disease (A-TLD (zeige BMP1 Antikörper)) is clinically similar to mild Ataxia-telangiectasia and caused by hypomorphic mutations in the MRE11 gene.
This gene encodes a nuclear protein involved in homologous recombination, telomere length maintenance, and DNA double-strand break repair. By itself, the protein has 3' to 5' exonuclease activity and endonuclease activity. The protein forms a complex with the RAD50 homolog\; this complex is required for nonhomologous joining of DNA ends and possesses increased single-stranded DNA endonuclease and 3' to 5' exonuclease activities. In conjunction with a DNA ligase, this protein promotes the joining of noncomplementary ends in vitro using short homologies near the ends of the DNA fragments. This gene has a pseudogene on chromosome 3. Alternative splicing of this gene results in two transcript variants encoding different isoforms.
meiotic recombination 11 homolog A
, MRE11 meiotic recombination 11 homolog A (S. cerevisiae)
, MRE11 homolog 1
, MRE11 homolog A
, double-strand break repair protein MRE11A
, meiotic recombination 11 homolog 1
, AT-like disease
, DNA recombination and repair protein
, endo/exonuclease Mre11
, meiotic recombination 11-like protein