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. Author manuscript; available in PMC: 2013 May 3.
Published in final edited form as: Genesis. 2011 Jun 21;49(7):546–554. doi: 10.1002/dvg.20766

Table 1.

Components of the expression vectors used in the study

* Expression vector p5E pME p3E
mnx1-3x125bp:prenEGFP mnx1-3x125-bp enhancer prenEGFP SV40 pA
mnx1-3x125bp:Gal4-VP16 mnx1-3x125-bp enhancer Gal4-VP16 SV40 pA
mnx1-782bp:prenEGFP mnx1-785-bp prenEGFP SV40 pA
mnx1-356bp-3x125bp:prenEGFP mnx1-356bp-3x125bp-enhancer prenEGFP SV40 pA
14xUAS:prenEGFP 14xUAS-E1b prenEGFP SV40 pA
*

Expressions vectors were generated by combining the elements in p5E, pME, and p3E plasmids into a pDestTol2pA2 vector via LR recombination.