P. R. Nicovich

This paper describes a low-cost DIY spinning disk confocal microscope module that enhances a standard epifluorescence microscope for 3D biological imaging.

This study shows that tropomyosin isoforms form distinct clusters on actin filaments due to their sequence similarity, not actin isoform preference.

This study uses fluorescence microscopy and modeling to quantify Tpm1.8 binding kinetics on actin filaments, revealing independent decoration of actin strands and asymmetric domain dynamics.

The paper introduces a hybrid light-sheet microscope that enables versatile multi-scale imaging of cleared tissues with varying resolution, geometry, and compatibility requirements.

The paper introduces a multi-immersion open-top light-sheet microscope for high-throughput imaging of cleared tissues using various clearing protocols.