Literature DB >> 18388942

Culture of Drosophila S2 cells and their use for RNAi-mediated loss-of-function studies and immunofluorescence microscopy.

Stephen L Rogers1, Gregory C Rogers.   

Abstract

Cultured Drosophila cell lines have become an increasingly popular model system for cell biological and functional genomic studies. One of the most commonly used lines, S2 cells, is particularly useful as it is easy to grow and maintain in the lab, is highly susceptible to gene inhibition using RNAi and is well suited to high-resolution light microscopic assays. Here, we provide protocols for the routine culture and RNAi treatment of S2 cells and methods to prepare these cells for fluorescence microscopy. Using these techniques, loss-of-function experiments may be performed after 4-7 d of RNAi-mediated protein depletion.

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Year:  2008        PMID: 18388942     DOI: 10.1038/nprot.2008.18

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  113 in total

1.  Preparation of Drosophila S2 cells for light microscopy.

Authors:  Daniel W Buster; Jonathan Nye; Joseph E Klebba; Gregory C Rogers
Journal:  J Vis Exp       Date:  2010-06-03       Impact factor: 1.355

2.  Using the Drosophila melanogaster D17-c3 cell culture system to study cell motility.

Authors:  Joshua D Currie; Stephen L Rogers
Journal:  Nat Protoc       Date:  2011-09-29       Impact factor: 13.491

3.  Extracellular Mipp1 Activity Confers Migratory Advantage to Epithelial Cells during Collective Migration.

Authors:  Yim Ling Cheng; Deborah J Andrew
Journal:  Cell Rep       Date:  2015-11-25       Impact factor: 9.423

4.  Unconventional myosin traffic in cells reveals a selective actin cytoskeleton.

Authors:  Crista M Brawley; Ronald S Rock
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-28       Impact factor: 11.205

5.  High throughput system for magnetic manipulation of cells, polymers, and biomaterials.

Authors:  Richard Chasen Spero; Leandra Vicci; Jeremy Cribb; David Bober; Vinay Swaminathan; E Timothy O'Brien; Stephen L Rogers; R Superfine
Journal:  Rev Sci Instrum       Date:  2008-08       Impact factor: 1.523

6.  RpL22e, but not RpL22e-like-PA, is SUMOylated and localizes to the nucleoplasm of Drosophila meiotic spermatocytes.

Authors:  Michael G Kearse; Jill A Ireland; Smrithi M Prem; Alex S Chen; Vassie C Ware
Journal:  Nucleus       Date:  2013-06-06       Impact factor: 4.197

7.  Gα12 structural determinants of Hsp90 interaction are necessary for serum response element-mediated transcriptional activation.

Authors:  Ellyn R Montgomery; Brenda R S Temple; Kimberly A Peters; Caitlin E Tolbert; Brandon K Booker; Joseph W Martin; Tyler P Hamilton; Alicia C Tagliatela; William C Smolski; Stephen L Rogers; Alan M Jones; Thomas E Meigs
Journal:  Mol Pharmacol       Date:  2014-01-16       Impact factor: 4.436

8.  Coordinate control of terminal dendrite patterning and dynamics by the membrane protein Raw.

Authors:  Jiae Lee; Yun Peng; Wen-Yang Lin; Jay Z Parrish
Journal:  Development       Date:  2014-12-05       Impact factor: 6.868

9.  Microtubule Acetylation Is Required for Mechanosensation in Drosophila.

Authors:  Connie Yan; Fei Wang; Yun Peng; Claire R Williams; Brian Jenkins; Jill Wildonger; Hyeon-Jin Kim; Jonathan B Perr; Joshua C Vaughan; Megan E Kern; Michael R Falvo; E Timothy O'Brien; Richard Superfine; John C Tuthill; Yang Xiang; Stephen L Rogers; Jay Z Parrish
Journal:  Cell Rep       Date:  2018-10-23       Impact factor: 9.423

10.  BCAS2 is essential for Drosophila viability and functions in pre-mRNA splicing.

Authors:  Po-Han Chen; Chia-I Lee; Yu-Tzu Weng; Woan-Yuh Tarn; Yeou-Ping Tsao; Ping-Chang Kuo; Pang-Hung Hsu; Chu-Wei Huang; Chiun-Sheng Huang; Hsiu-Hsiang Lee; June-Tai Wu; Show-Li Chen
Journal:  RNA       Date:  2012-12-17       Impact factor: 4.942

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