Imaging- Confocal

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Description

Protocol for imaging using confocal microscope. Sections for analysis should be mounted on slides, stained for appropriate markers, and coverslipped. This protocol is using a Carl Zeiss LSM 880 confocal microcope.

Identifier (DOI)

10.17504/protocols.io.j8nlk88y1l5r/v1

Tags

Microscopy - optical

Team

Team Kaplitt

Program

Collaborative Research Network

Theme

Circuitry and Brain-Body Interactions

Meet the Authors

Daniel Dautan

Key Personnel: Team Kaplitt,

Karolinska Institute
Per Svenningsson, MD, PhD

Co-PI (Core Leadership): Team Kaplitt,

Karolinska Institute

Imaging- Confocal

Output Details

Meet the Authors

Daniel Dautan

Per Svenningsson, MD, PhD

Related Research

Mouse brain immunohistochemistry – colorimetric analysis

Primary data1: Pathogenic LRRK2 mutations cause loss of primary cilia and Neurturin in striatal parvalbumin interneurons

Primary data2: Pathogenic LRRK2 mutations cause loss of primary cilia and Neurturin in striatal parvalbumin interneurons