碘化丙啶
多聚甲醛
DNA
溶解
化学
分子生物学
染色
固定(群体遗传学)
污渍
生物
生物化学
细胞凋亡
遗传学
程序性细胞死亡
基因
有机化学
作者
Awtar Krishan,Ronald M. Hamelik
标识
DOI:10.1002/0471142956.cy0736s52
摘要
The Click-iT EdU cell proliferation assay (Invitrogen) for detection of replicating cells is based on incorporation of EdU into newly synthesized DNA and its recognition by azide dyes via a copper mediated "click" reaction. In the protocol provided by Invitrogen, cells are fixed with paraformaldehyde and stained with 7-aminoactinomycin D (7-AAD) for DNA content analysis. Both of these procedures result in DNA histograms with a broad coefficient of variation. We have modified this protocol and show that after EdU incorporation, nuclei isolated by hypotonic lysis of cells can be directly labeled using the Click-iT Alexa Fluor 488 Assay kit and stained with propidium iodide. This modified procedure using isolated nuclei and propidium iodide staining results in DNA histograms with better resolution (lower coefficient of variation of the G(1) peak) and shorter processing time by eliminating the fixation and permeabilization steps.
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