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Updated: Oct 8, 2025

Assessing Autophagic Flux by Measuring LC3, p62, and LAMP1 Co-localization Using Multispectral Imaging Flow Cytometry
Published on: July 21, 2017
A Dual HiBiT-GFP-LC3 Lentiviral Reporter for Autophagy Flux Assessment
Rainer Will1, Katja Bauer2, Matthias Kudla3
1Cellular Tools, Genomics and Proteomics Core Facility, German Cancer Research Center (DKFZ), Heidelberg, Germany. R.Will@dkfz.de.
Abstract:
Autophagy is an intracellular degradation process that maintains the cellular homeostasis and it is regulated in multiple ways, both in health and disease. Assessment of autophagic flux in cells is an important approach for understanding the function of autophagy in biological contexts. Here, we describe a new tool for the qualitative and quantitative determination of autophagic flux using a dual lentiviral reporter system that generates a fusion HiBiT-GFP-LC3B protein suitable for generating stable cell lines.

