可视化
荧光
荧光寿命成像显微镜
活体细胞成像
有丝分裂
材料科学
生物物理学
纳米技术
细胞生物学
计算机科学
光学
生物
细胞
物理
人工智能
遗传学
作者
Kapil Kumar,Thomas Hartig Braunstein,Pablo Hernández-Varas,Mikkel Baldtzer Liisberg,Bo W. Laursen
摘要
and the mechanism of binding interactions was investigated using CD spectroscopy. The long fluorescence lifetime and excellent biocompatibility of Nuc-DAOTA+ enabled its use for real-time dynamic imaging of mitotic phases and interphase in live CHO (Chinese hamster ovary) cells by using confocal microscopy. In addition, the Nuc-DAOTA+ exhibited high photostability during photo-bleaching experiments and was successfully applied for fluorescence lifetime imaging microscopy (FLIM) and time gated imaging of the mouse embryonic fibroblast 3T3 cell line.
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