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首页> 外文期刊>BioTechniques >Detection of S-phase cell cycle progression using 5-ethynyl-2'-deoxyuridine incorporation with click chemistry, an alternative to using 5-bromo-2'-deoxyuridine antibodies.
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Detection of S-phase cell cycle progression using 5-ethynyl-2'-deoxyuridine incorporation with click chemistry, an alternative to using 5-bromo-2'-deoxyuridine antibodies.

机译:使用5-乙炔基-2'-脱氧尿苷与点击化学结合检测S期细胞周期进程,是使用5-溴-2'-脱氧尿苷抗体的替代方法。

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摘要

The 5-bromo-2'-deoxyuridine (BrdU) labeling of cells followed by antibody staining has been the standard method for direct measurement of cells in the S-phase. Described is an improved method for the detection of S-phase cell cycle progression based upon the application of click chemistry, the copper(I)-catalyzed variant of the Huisgen [3+2] cycloaddition between a terminal alkyne and an azide. 5-ethynyl-2'-deoxyuridine (EdU) is a nucleoside analog of thymidine that is incorporated into DNA during active DNA synthesis, just like BrdU. While the BrdU assay requires harsh chemical or enzymatic disruption of helical DNA structure to allow for direct measurement of cells in the S-phase by the anti-BrdU antibody, the EdU method does not. Elimination of this requirement results in the preservation of helical DNA structure and other cell surface epitopes, decreased assay time, and increased reproducibility.
机译:对细胞进行5-溴-2'-脱氧尿苷(BrdU)标记,然后进行抗体染色,已成为直接测量S期细胞的标准方法。描述了一种基于点击化学的应用,用于检测S期细胞周期进程的改进方法,点击化学是末端炔烃与叠氮化物之间的Huisgen [3 + 2]环加成反应的铜(I)催化变体。 5-乙炔基-2'-脱氧尿苷(EdU)是胸苷的核苷类似物,与BrdU一样,在活性DNA合成过程中被掺入DNA中。虽然BrdU分析需要严格的化学或酶促破坏螺旋DNA结构才能通过抗BrdU抗体直接测量S期细胞,但EdU方法却不需要。消除此要求可保留螺旋DNA结构和其他细胞表面表位,减少测定时间并提高重现性。

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