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2 protocols using sd gal4

1

Drosophila Genetic Manipulations

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All stocks were raised on standard Drosophila media and crosses were performed at 25°C unless otherwise indicated. UAS-APLP1, UAS-APPLsd were kindly provided by Dr. Merdes [22 (link)]; pucH246, UAS-mmp1-IR, UAS-mmp2-IR, UAS-TIMP1, UAS-RasV12, UAS-Rho1-IR, UAS-p35, UAs-P53DN were obtained from Bloomington Stock Center; sd-Gal4, UAS-BskDN, UAS-Puc, UAS-Egr, UAS-Hep [70 (link)]; ptc-Gal4, en-Gal4, pucE69 34, UAS-LacZ [71 (link)] were previously described.
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2

Mosaic Transgene Expression in Drosophila Imaginal Discs

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Drosophila stocks were maintained by standard methods at 25°C. For generation of mosaic UAS-transgene overexpression clones in imaginal discs, first instar larvae (48 h after egg deposition) were heat-shocked for 15–60 min at 37°C. To control the timing of UAS-transgene overexpression with the temperature-sensitive Gal80 (Gal80ts) in imaginal discs, fly larvae were kept in 18°C until they reached second instar stage and were then transferred to 29°C. The following fly strains were used: ptc-Gal4 (Bloomington #2017), sd-Gal4 (Bloomington #8609), en-Gal4 (Bloomington #30564), act-Gal4 (Bloomington #4414), UAS-RhoGEF2-RNAi (Bloomington #34643), UAS-rpr (Bloomington #5823), UAS-lgl-RNAi (VDRC #51247), UAS-scrib-RNAi (VDRC #105412), UAS-STAT92E-RNAi (VDRC #106980), UAS-YkiM123 [51 (link)], UAS-3HA-STAT92EΔNΔC [27 (link)], 10xSTAT-GFP [22 (link)], and vkg-GFP (G00454). All genotypes of flies used in each experiment are described below.
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