| Literature DB >> 34972942 |
Debadrita Pal1, Florencia Visconti1, Silvia P Sepúlveda-Ramírez1, S Zachary Swartz2, Charles B Shuster3.
Abstract
The early embryos of sea urchins and other echinoderms have served as experimental models for the study of cell division since the nineteenth century. Their rapid development, optical clarity, and ease of manipulation continue to offer advantages for studying spindle assembly and cytokinesis. In the absence of transgenic lines, alternative strategies must be employed to visualize microtubules and actin. Here, we describe methods to visualize actin and microtubule using either purified, recombinant proteins, or probes in in vitro-transcribed mRNAs.Entities:
Keywords: Confocal microscopy; Cytokinesis actin; Meiosis; Microtubule; Mitosis; Sea star; Sea urchin
Mesh:
Year: 2022 PMID: 34972942 DOI: 10.1007/978-1-0716-1904-9_1
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745