February 20th, 2018
•This protocol describes a method for the photoconversion of Kaede fluorescent protein in endocardial cells of the living zebrafish embryo that enables the tracking of endocardial cells during atrioventricular canal and atrioventricular heart valve development.
Related Videos
Measuring Protein Stability in Living Zebrafish Embryos Using Fluorescence Decay After Photoconversion (FDAP)
Microbead Implantation in the Zebrafish Embryo
Imaging Subcellular Structures in the Living Zebrafish Embryo
Observing Mitotic Division and Dynamics in a Live Zebrafish Embryo
Visualizing the Interrenal Steroidogenic Tissue and Its Vascular Microenvironment in Zebrafish
Use of Immunolabeling to Analyze Stable, Dynamic, and Nascent Microtubules in the Zebrafish Embryo
Live Imaging of Mouse Secondary Palate Fusion
AFM and Microrheology in the Zebrafish Embryo Yolk Cell
Single-cell Photoconversion in Living Intact Zebrafish
Microinjection-based System for In Vivo Implantation of Embryonic Cardiomyocytes in the Avian Embryo
Copyright © 2024 MyJoVE Corporation. 판권 소유