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抗Mouse (Murine) Topoisomerase II alpha 抗体:
抗Rat (Rattus) Topoisomerase II alpha 抗体:
抗Human Topoisomerase II alpha 抗体:
Human Polyclonal Topoisomerase II alpha Primary Antibody for ICC, IF - ABIN4361369
Lindén, Segersten, Runeson, Wester, Busch, Pettersson, Lind, Malmström: Tumour expression of bladder cancer-associated urinary proteins. in BJU international 2013
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Human Monoclonal Topoisomerase II alpha Primary Antibody for IF, IHC (p) - ABIN563224
Poonperm, Takata, Hamano, Matsuda, Uchiyama, Hiraoka, Fukui: Chromosome Scaffold is a Double-Stranded Assembly of Scaffold Proteins. in Scientific reports 2015
Arabidopsis thaliana Polyclonal Topoisomerase II alpha Primary Antibody for IL, WB - ABIN334538
Xie, Lam: Abundance of nuclear DNA topoisomerase II is correlated with proliferation in Arabidopsis thaliana. in Nucleic acids research 1995
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Polyamide functionalisation at the N1-position offers a design strategy to improve drug-like properties. Dicationic HxIP* 3 increased topo IIalpha expression and chemosensitivity to topo II (显示 TOP2 抗体)-targeting agents.
We demonstrated that Nup98 (显示 NUP98 抗体)-TopIIbeta and Nup98 (显示 NUP98 抗体)-SETBP1 (显示 SETBP1 抗体) negatively regulate the XPO1 (显示 XPO1 抗体)-mediated protein export. Our results will contribute to the understanding of the molecular mechanism by which the Nup98 (显示 NUP98 抗体)-fusion proteins induce tumorigenesis.
TOP2 (显示 TOP2 抗体) and BAF (显示 BANF1 抗体) cooperate to recruit pluripotency factors, which explains some of the instructive roles of BAF (显示 BANF1 抗体) complexes.
Deletion or deficiency of PTEN (显示 PTEN 抗体) leads to down regulation of TOP2A, dysfunction of the decatenation checkpoint and incomplete DNA decatenation in G2 and M phases.
Inhibition of DNA topoisomerase II (显示 TOP2 抗体) selectively reduces the threat of tumorigenicity
Cohesin removal is a prerequisite for the posterior topoisomerase IIalpha-mediated resolution of persisting catenations between segregating chromatids during anaphase II.
Data show that unfolded protein response (UPR)-induced changes in topoisomerase IIalpha (Topo IIalpha) protein levels are not responsible for resistance to etoposide, and that the PERK plays a Topo IIalpha-independent role in altered sensitivity to the drug.
TOP2beta (显示 TOP2B 抗体) as a factor involved in regulating granulosa cell genomic integrity and follicle atresia.
Topoisomerase IIa not only contributes to stem-cell transcriptome regulation but also primes developmental genes for subsequent activation upon differentiation.
studies indicate that the ability of TOP2A to prevent DNA entanglement at mitosis requires BAF (显示 BANF1 抗体) complexes and suggest that this activity contributes to the role of BAF (显示 BANF1 抗体) subunits as tumour suppressors
Data show that comparing with Ki-67 (显示 MKI67 抗体) and TOP2A, RacGAP1 (显示 RACGAP1 抗体) allowed for a clearer prognostic statement.
These findings reveal a novel, p53 (显示 TP53 抗体)-independent activity of Mdm2 (显示 MDM2 抗体) and have important implications for the choice of chemotherapeutic agents in the treatment of Mdm2 (显示 MDM2 抗体)-overexpressing tumors. Herein is shown that tumor cells with MDM2 (显示 MDM2 抗体) amplification are selectively resistant to treatment with topoisomerase II (显示 TOP2 抗体) poisons but not other DNA damaging agents
The methodology is useful for a high-throughput analysis of drugs that poison Top2, allowing not just the discrimination of the Top2 isoform that is targeted but also to track its removal
TOP2A was identified in association with the progression and prognosis of pancreatic ductal adenocarcinoma probably by regulating cell cycle and p53 (显示 TP53 抗体) signaling pathway.
the relation between TOP2A levels and sensitivity for doxorubicin was examined, confirming reports that TOP2A mRNA levels were overexpressed in MPNST and showing that MPNST cell lines exhibited relatively high TOP2A protein levels and sensitivity to doxorubicin.
The decatenation checkpoint is regulated, not only by topo IIalpha, as previously reported, but also by topo IIbeta. The decatenation checkpoint is most efficient when both isoforms are present. Deletion of most of the C-terminus of topo IIalpha, while preserving the nuclear localization signal (NLS (显示 ALDH1A2 抗体)), enhances the decatenation checkpoint and sensitivity to topo II (显示 TOP2 抗体)-targeted drugs. Mutation of Y640 in topo IIalpha inhibi...
Tumors with higher topoisomerase IIalpha and/or mitosin (显示 CENPF 抗体) expression have a higher risk of recurrence after initial treatment, and these patients may benefit from adjuvant treatment and closer radiological follow-up
Both the genome instability and cell death of MRE11 (显示 MRE11A 抗体)-null and MRE11 (显示 MRE11A 抗体)-mutated H129N cells are significantly reversed by overexpression of Tdp2 (显示 TDP2 抗体), an enzyme that eliminates covalent Top2 conjugates; thus, the essential role of Mre11 (显示 MRE11A 抗体) nuclease (显示 DCLRE1C 抗体) activity is likely to remove the DNA lesions.
we show that TopoIIalpha forms protein-protein interactions with beta-catentin and TCF4 (显示 TCF4 抗体) and interacts with Wnt (显示 WNT2 抗体) response elements (WREs) and promoters of direct target genes of TCF (显示 HNF4A 抗体) transcription, including: MYC (显示 MYC 抗体), vimentin (显示 VIM 抗体), AXIN2 (显示 AXIN2 抗体) and LEF1 (显示 LEF1 抗体)
This study shows that both survivin (显示 BIRC5 抗体) and TIIalpha are independent prognostic predictors in human grade II/III astrocytomas stratified for IDH1 (显示 IDH1 抗体)-mutation status
This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This nuclear enzyme is involved in processes such as chromosome condensation, chromatid separation, and the relief of torsional stress that occurs during DNA transcription and replication. It catalyzes the transient breaking and rejoining of two strands of duplex DNA which allows the strands to pass through one another, thus altering the topology of DNA. Two forms of this enzyme exist as likely products of a gene duplication event. The gene encoding this form, alpha, is localized to chromosome 17 and the beta gene is localized to chromosome 3. The gene encoding this enzyme functions as the target for several anticancer agents and a variety of mutations in this gene have been associated with the development of drug resistance. Reduced activity of this enzyme may also play a role in ataxia-telangiectasia.
DNA topoisomerase II, alpha isozyme
, DNA Topoisomerase II alpha
, DNA topoisomerase 2-alpha
, topoisomerase (DNA) 2 alpha
, DNA gyrase
, DNA topoisomerase (ATP-hydrolyzing)
, DNA topoisomerase II, 170 kD
, DNA topoisomeraseII_alpha
, DNA topoisomerase 2-beta
, DNA topoisomerase II, beta isozyme