Larval body wall dissection at 3-fold time-lapse.

M Marter et al.

DOI: 10.21769/BioProtoc.v210 Published: Jan 20, 2019 Views: 3196

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A wet larva is placed on the dissection chamber shown in the supplementary figure. Using the central, straight clips the animal is immobilized and moderately stretched, dorsal side up. The animal is then covered with Ca2+-free saline. Using the spring scissors a hole is squeezed in at about 75% length, serving as a starting point for cutting along the dorsal midline, first direction mouth hook and then towards the posterior end. Short incisions are made to the right and the left at either end. To avoid scratching the body wall muscles and harming the larval brain with the blades, the scissors are slightly lifted during the cutting. Once cut, the larva is pushed a bit to squeeze out inner organs such as the gut and fat body and thus to ease their removal. The lateral clips are then used to carefully span the body wall.

Extracted from protocol
Click Chemistry (CuAAC) and Detection of Tagged de novo Synthesized Proteins in Drosophila
Marter, K., Kobler, O., Erdmann, I., Soleimanpour, E., Landgraf, P., Müller, A., Abele, J., Thomas, U. and Dieterich, D. C. (2019). Bio-protocol 9(2): e3142.
DOI: 10.21769/BioProtoc.3142.

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Keywords

Bio-orthogonal chemical reporters, Click chemistry, CuAAC, Protein tagging, Drosophila melanogaster, Proteomic profiling, Protein synthesis

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