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Titlebook: DNA Topoisomerases; Methods and Protocol Duncan J. Clarke Book 2009 Humana Press 2009 Cellular functions.Chromosom.Chromosome structure.DNA

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樓主: 譴責
31#
發(fā)表于 2025-3-26 22:02:44 | 只看該作者
32#
發(fā)表于 2025-3-27 03:52:22 | 只看該作者
Analysis of DNA Topoisomers, Knots, and Catenanes by Agarose Gel Electrophoresis,l-molecule ligands, analyzing conformational transitions in duplex DNA, measuring changes in helical repeat that accompany shifts in environmental conditions, and characterizing knotting and linking in duplex DNA.
33#
發(fā)表于 2025-3-27 05:24:52 | 只看該作者
Two-Dimensional Agarose Gel Electrophoresis of DNA Topoisomers,eps are conducted in orthogonal directions with different concentrations of DNA intercalating agents. These compounds alter the overall shape of the DNA and, thereby, change the relative mobility of individual DNA topoisomers.
34#
發(fā)表于 2025-3-27 10:35:32 | 只看該作者
Assays for the Preferential Binding of Human Topoisomerase I to Supercoiled DNA,filter binding assay compares the ability of nicked and supercoiled forms of the circular DNA to compete for the binding of a .H-labeled nicked DNA to the topoisomerase where the enzyme–DNA complexes are quantitated by the retention of the labeled DNA on a nitrocellulose membrane.
35#
發(fā)表于 2025-3-27 15:59:54 | 只看該作者
36#
發(fā)表于 2025-3-27 18:21:08 | 只看該作者
Studies in Computational Intelligenceoint using spindle morphology, chromosome condensation using fluorescently labeled chromosomal loci, and cell cycle progression by flow cytometry. Further characterization of this novel checkpoint is warranted so that we can further our understanding of the cell cycle, genomic stability, and the possibility of identifying novel drug targets.
37#
發(fā)表于 2025-3-27 22:03:48 | 只看該作者
38#
發(fā)表于 2025-3-28 03:44:40 | 只看該作者
39#
發(fā)表于 2025-3-28 08:59:57 | 只看該作者
Bahaaeddin Alareeni,Allam Hamdantterned photobleaching, LPk-GT2 cells were used to demonstrate the rapid dynamics of Topo IIα exchange in both interphase nuclei and mitotic chromosomes. These rapid dynamics are dependent on enzyme activity since ICRF159, a catalytic inhibitor of Topo IIα, slows dynamics significantly. The methods utilized in these studies are described herein.
40#
發(fā)表于 2025-3-28 10:55:49 | 只看該作者
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