Cite as: Cold Spring Harb. Protoc.; 2007; doi:10.1101/pdb.prot4712

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Preparing Cytoplasmic Extracts from Drosophila Embryos

Michelle Moritz

This protocol was adapted from "Preparing Cytoplasmic Extracts from Drosophila Embryos," Chapter 33, in Drosophila Protocols (eds. Sullivan et al.). Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2000.


INTRODUCTION

In recent years, Drosophila has been an excellent source for biochemical quantities of proteins involved in a variety of cellular processes, such as cytoskeletal function and RNA binding. It is relatively simple to obtain a high-quality Drosophila embryonic cytoplasmic extract for protein purification or biochemistry, if population cages are used that produce at least 5 g of embryos during a 3-hour period. Smaller quantities of embryos can be used to produce extracts for in vitro biochemical assays. This protocol describes the collection and dechorionation of Drosophila embryos and the preparation of cytoplasmic extracts.


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