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. 2023 Jan 6;13(3):jkad003. doi: 10.1093/g3journal/jkad003

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© The Author(s) 2023. Published by Oxford University Press on behalf of the Genetics Society of America.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 3. — Comparison of Gal4 and converted LexA and Flp lines in non-neural tissues. a–a″) Activity patterns of esg-Gal4 (a), esg-LexAGAD (a′), and esg-Flp1 (a″) in the whole larval body. b and b′) Activity patterns of Mef2-Gal4 (b) and Mef2-LexAGAD (b′) in the whole larval body. c and c′) Activity patterns of Dcg-Gal4 (c) and Dcg-LexAGAD (c′) in the whole larval body. d–d″) Activity patterns of wg-Gal4 (d), wg-LexAGAD (d′), and wg-Flp1 (d″) in epidermal cells of a single hemisegment. Arrowhead (d″) indicates the cell body of a sensory neuron. e–e″) Activity patterns of R28E04-Gal4 (e), R28E04-LexAGAD (e′), and R28E04-Flp1 (e″) in epidermal cells of a single hemisegment. f–f″) Activity patterns of R16D01-Gal4 (f) and R16D01-LexAGAD (f′) in epidermal cells of a single hemisegment. Refer to Table 1 for reporter lines used. Scale bar: 300 μm (a–c′); 100 μm (d–f′).