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DOI: 10.3791/54042-v
Allison S. Harney1,2,3,4, Yarong Wang1,3, John S. Condeelis1,3,4, David Entenberg1,3,4
1Department of Anatomy & Structural Biology,Albert Einstein College of Medicine, 2Department of Radiology,Albert Einstein College of Medicine, 3Gruss-Lipper Biophotonics Center,Albert Einstein College of Medicine, 4Integrated Imaging Program,Albert Einstein College of Medicine
Please note that some of the translations on this page are AI generated. Click here for the English version.
This protocol describes the use of multiphoton microscopy to visualize dynamic events within the tumor microenvironment in real time. The technique allows for extended time-lapse imaging at single cell resolution, providing insights into vascular permeability and multicellular interactions.
Este protocolo describe el uso de la microscopía multifotónica para realizar extendida time-lapse de las interacciones multicelulares en tiempo real, en vivo a una resolución de una sola célula.
El objetivo general de este procedimiento es visualizar los eventos dinámicos dentro del microambiente tumoral a través de microspy multifotónico intravital de alta resolución. Este método puede ayudar a responder preguntas clave sobre el microambiente tumoral, como qué eventos dinámicos están involucrados en la permeabilidad vascular y las interacciones multicelulares. La principal ventaja de esta técnica es que se puede observar y medir la cinética de los eventos en el microambiente tumoral.
Antes de comenzar el procedimiento, encienda todos los componentes del microscopio y del láser, incluidos los dos láseres de fotones y los detectores. Y ajuste la caja de calefacción a 30 grados centígrados para precalentar el escenario. Limpie la platina del microscopio y el inserto de la platina con etanol al 70%.
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