Home›Analytical Chem›Visualization of Proprioceptors in Drosophila Larvae and Pupae
Analytical ChemJoVE (Open Access)Citable · DOI
Visualization of Proprioceptors in Drosophila Larvae and Pupae
DOI: 10.3791/3846-v
What you'll learn
✓Dissect and fix Drosophila larvae and pupae for immunostaining
✓Perform immunostaining to visualize chordotonal organs
✓Mount and image proprioceptor tissue using confocal microscopy
Protocol
A method to immunostain and visualize chordotonal organs in larvae and pupae of Drosophila melanogaster is described.
Difficulty
intermediate
Total time
~4–6 hours (dissection through imaging per cohort)
Model organism
Drosophila melanogaster
Biosafety
BSL-1
Steps
1
Dissect and fix third instar larvae
Remove third instar larvae from culture medium, dissect to expose nervous tissue, and fix in appropriate fixative solution to preserve chordotonal organ morphology.
▶ 01:02
2
Dissect and fix pupae
Extract pupae from substrate, perform careful dissection to access proprioceptor-containing tissues, and apply fixation protocol optimized for pupal developmental stage.
▶ 03:22
3
Mount immunostained larvae and pupae
Arrange fixed, antibody-labeled tissue on microscope slides and apply mounting medium appropriate for fluorescence imaging.
▶ 06:43
4
Image and analyze chordotonal organ visualization
Acquire confocal or epifluorescence micrographs of labeled proprioceptor organs and examine morphological features across developmental stages.
▶ 07:52
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