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使用5-乙炔基-2'-脱氧尿苷掺入并结合点击化学检测S期细胞周期进程,这是一种替代使用5-溴-2'-脱氧尿苷抗体的方法。

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.

作者信息

Buck Suzanne B, Bradford Jolene, Gee Kyle R, Agnew Brian J, Clarke Scott T, Salic Adrian

机构信息

Invitrogen Corporation, Eugene, OR 97402, USA.

出版信息

Biotechniques. 2008 Jun;44(7):927-9. doi: 10.2144/000112812.

Abstract

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.

摘要

细胞经5-溴-2'-脱氧尿苷(BrdU)标记后进行抗体染色,一直是直接测量处于S期细胞的标准方法。本文描述了一种基于点击化学(末端炔烃与叠氮化物之间的铜(I)催化的Huisgen [3+2]环加成变体)来检测S期细胞周期进程的改进方法。5-乙炔基-2'-脱氧尿苷(EdU)是胸腺嘧啶核苷类似物,在活跃的DNA合成过程中会掺入DNA,就像BrdU一样。虽然BrdU检测需要对螺旋DNA结构进行苛刻的化学或酶促破坏,以便通过抗BrdU抗体直接测量处于S期的细胞,但EdU方法则不需要。消除这一要求可保留螺旋DNA结构和其他细胞表面表位,减少检测时间,并提高重现性。

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