Beisker W, Eisert W G
Anal Quant Cytol. 1981 Dec;3(4):315-22.
Fluorescence polarization measurements using high-speed single-cell flow cytometry have found increasing use in cellular biology. In most flow systems, the detection axis generally is aligned orthogonally to the direction of flow and the excitation axis, and asymmetric apertures along the excitation and emission axes by cylindrical lenses and/or nonplanar transition between optical indices complicate the numerical correction of systematic depolarization effects. In addition, recent studies on fluorescence emission of structured particles have shown remarkable anisotropies of polarized fluorescence emission dependent on the direction of the detection axis.
利用高速单细胞流式细胞术进行的荧光偏振测量在细胞生物学中的应用越来越广泛。在大多数流动系统中,检测轴通常与流动方向和激发轴正交,并且柱面透镜沿激发轴和发射轴的不对称孔径和/或光学折射率之间的非平面过渡使系统去极化效应的数值校正变得复杂。此外,最近关于结构化颗粒荧光发射的研究表明,偏振荧光发射的各向异性显著依赖于检测轴的方向。