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. Author manuscript; available in PMC: 2017 Jan 5.
Published in final edited form as: Mol Cell Endocrinol. 2015 Oct 22;419:124–138. doi: 10.1016/j.mce.2015.10.006

Fig. 3.

Fig. 3

Comparison of CRE recombinase activity assayed in vivo by fluorescence visualization of tdTomato (indicated as RFP) to GFP conversion during embryonic pituitary development in three different gonadotrope-specific Cre-deleter mouse strains on an mT/mG genetic background (A–C). A representative example of pituitary harvested at each embryonic time point from each strain is shown. White box (in C) shows a group of GFP+ gonadotropes in pituitary of an Fshb-Cre+ mouse embryo at E14.5. White bar = 2mm.