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. Author manuscript; available in PMC: 2009 Apr 20.
Published in final edited form as: Mol Endocrinol. 2009 Jan 15;23(4):529–538. doi: 10.1210/me.2008-0399

Figure 6.

Figure 6

In vivo and ex vivo imaging of reporter genes in LPS treated PRL-Luc/d2eGFP double transgenic rats. a) In vivo imaging of vehicle (V) and LPS-treated rats. The rats were injected i.p either with physiological saline or with 3mg/ml LPS and imaged 16 h after the treatment. The images were acquired with an IVIS Spectrum (Xenogen/ Caliper): 30s integration time, Bin (HR) 8, FOV 19.6, f1. b) Flow cytometric analysis of d2eGFP positive cells from the peritoneal exudate of a vehicle and a LPS treated double transgenic rats. c) Confocal imaging of cytocentrifuge preparation of cells from the peritoneal exudate of LPS treated double-transgenic rats. Scale bar, 10μm.