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University of North Carolina at Chapel Hill

7 ARTICLES PUBLISHED IN JoVE

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Biology

Affinity Precipitation of Active Rho-GEFs Using a GST-tagged Mutant Rho Protein (GST-RhoA(G17A)) from Epithelial Cell Lysates
Faiza Waheed 1,2, Pamela Speight 1,2, Qinghong Dan 1,2, Rafael Garcia-Mata 3, Katalin Szaszi 1,2
1Keenan Research Centre, Li Ka Shing Knowledge Institute, St. Michael's Hospital , 2Department of Surgery, University of Toronto, 3Department of Cell and Developmental Biology, University of North Carolina at Chapel Hill

The method presented here describes an assay to follow activation of RhoA specific GDP/GTP Exchange Factors (GEFs) in cultured cells by making use of a mutant RhoA GST fusion protein that has high affinity for activated GEFs. GEFs are precipitated from cell lysates, detected by Western blotting and quantified by densitometry.

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Biology

Microgavage of Zebrafish Larvae
Jordan L. Cocchiaro 1, John F. Rawls 1
1Department of Cell and Molecular Physiology, University of North Carolina at Chapel Hill

We present a novel method for microgavage of larval zebrafish utilizing standard embryo microinjection and stereomicroscopy equipment. We demonstrate that microgavage is a safe and efficient technique useful for delivering controlled amounts of diverse materials specifically into the larval zebrafish intestinal lumen.

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Biology

A Novel Ex vivo Culture Method for the Embryonic Mouse Heart
Laura A. Dyer 1, Cam Patterson 1
1McAllister Heart Institute, University of North Carolina at Chapel Hill

Developmental studies in the mouse are hampered by the inaccessibility of the embryo during gestation. To promote the long-term culture of the embryonic heart at late stages of gestation, we developed a protocol in which the excised heart is cultured in a semi-solid, dilute Matrigel.

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Biology

Isolation of Embryonic Ventricular Endothelial Cells
Laura A. Dyer 1, Cam Patterson 1
1McAllister Heart Institute, University of North Carolina at Chapel Hill

Primary cell culture is a useful technique for analyzing specific populations of cells, particularly from transgenic mouse embryos at specific developmental stages. Herein, embryonic ventricles are dissected and dissociated, and antibody-conjugated beads recognize and separate out the endothelial cells for further analysis.

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Biology

Intravital Microscopy for Imaging Subcellular Structures in Live Mice Expressing Fluorescent Proteins
Andrius Masedunskas 1,2, Natalie Porat-Shliom 1, Muhibullah Tora 1, Oleg Milberg 1,3, Roberto Weigert 1
1Intracellular Membrane Trafficking Unit, Oral and Pharyngeal Cancer Branch National Institute of Dental and Craniofacial Research, National Institutes of Health, 2Department of Biology, University of North Carolina at Chapel Hill , 3Department of Chemical & Biochemical Engineering and Department of Biomedical Engineering, Rutgers University

Intravital microscopy is a powerful tool that enables imaging various biological processes in live animals. In this article, we present a detailed method for imaging the dynamics of subcellular structures, such as the secretory granules, in the salivary glands of live mice.

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Biology

Using Coculture to Detect Chemically Mediated Interspecies Interactions
Elizabeth Anne Shank 1
1Department of Biology, University of North Carolina at Chapel Hill

Bacteria produce secreted compounds that have the potential to affect the physiology of their microbial neighbors. Here we describe a coculture screen that allows detection of such chemically mediated interspecies interactions by mixing soil microbes with fluorescent transcriptional reporter strains of Bacillus subtilis on solid media.

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Biology

Protein Isolation from the Developing Embryonic Mouse Heart Valve Region
Laura A. Dyer 1, Yaxu Wu 1, Cam Patterson 2
1McAllister Heart Institute, University of North Carolina at Chapel Hill, 2New York-Presbyterian Hospital/Weill-Cornell Medical Center

The analysis of protein expression in young embryonic mouse valves has been hampered by the limited tissue available. This manuscript provides a protocol for preparing protein from developing embryonic mouse valve regions for western blot analysis.

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