10.7.2023 - 14.7.2023

EMBL Course: Fluorescence imaging beyond intensity

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Date:
10.-14.07.2023
Location: EMBL Heidelberg
Venue: EMBL Advanced Training Centre
Deadline: Aplication by 17. Apr 2023 

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This course is organised by EMBL in cooperation with Leica Microsystems.

Course overview

As fluorescence lifetime-based readouts become more accessible, this course aims to provide a broad understanding of how the lifetime-based information can be leveraged to solve biological questions. This application-centred course will provide insights into how this additional dimension of fluorescence information can help unveil functional and mechanistic information.

Audience

This course is aimed at PhD students and Post Docs with experience in fluorescence microscopy. It will enable them to better apply confocal fluorescence microscopy and in particular lifetime-based readouts to their cutting-edge research, disseminate their gained expertise to colleagues at their home institution and, eventually, to develop imaging methods beyond the state-of-the-art.

PRELIMITARY PROGRAMME


Modules/resources

  • Measuring protein-protein interactions
  • Environmental sensing with FRET-based and non-FRET-based biosensors
  • Using fluorescence lifetime for multiplexing
  • Increasing the resolution with tauSTED
  • Endogenous fluorescence – harnessing additional information and removing unwanted fluorescence like autofluorescence and background fluorescence
  • Sessions at the microscopes to practice using lifetime imaging in exemplary workflows
  • Analysis of the lifetime-based information and applicative conclusions

Learning outcomes

  • Understand the basics of fluorescence lifetime
  • Identify which types of research questions and approaches can benefit from lifetime-related measurements and how to design such experiments
  • Learn to use common biosensors, probes and fluorophores and understand the additional information and contrast provided by fluorescence lifetime
  • Understand the basis of endogenous fluorescence (in particular in tissue and animal models) and how fluorescence lifetime can help to exploit or cope with their signals
  • Acquire and analyze lifetime-related information in different experimental setups

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