Immunofluorescence and confocal microscopy

By Elias Adriaenssens, PhD
View Published Protocol

Output Details

Description
This protocol details the process of immunofluorescence and confocal microscopy.
Identifier (DOI)
10.17504/protocols.io.6qpvr8p1olmk/v1
Tags
  • Confocal microscopy
  • Immunofluorescence
  • Other
Team
Team Hurley
Program
Collaborative Research Network
Theme
PD Functional Genomics

Meet the Authors

  • User avatar fallback logo

    Elias Adriaenssens, PhD

    Key Personnel: Team Hurley, 

    Max F. Perutz Laboratories

Related Research

Confocal microscopy to assess TelC and iGluSnFR expression in fixed mouse brain slices

Protocol outlines tissue processing after glutamate recordings with iGluSnFR sensor & behavior experiments post TelC viral injection in dorsal medial striatum.

View Protocol

Source data for Motor Cortical Neuronal Hyperexcitability Associated with α-Synuclein Aggregation

Chen et al (2024) study links α-synuclein aggregation to hyperexcitability in motor cortical neurons.

View Dataset

Single-cell Whole Genome Amplification (scWGA) of human post-mortem brain samples isolated by Laser Capture Microdissection (LCM)

This protocol uses Laser Capture Microdissection (LCM) technology on human post-mortem brain tissue slides in order to do low coverage single-cell whole genome sequencing to detect mega-base somatic Copy Number Variations (CNVs).

View Protocol
View More Outputs
Aligning Science Across Parkinson's
Powered by  GDPR Cookie Compliance
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.