Pregnant ICR mice (Nihon SLC) were reared under a normal 12 h light/dark cycle. The day of insemination was designated as embryonic day (E) 0. One mM ATV or 1 mM ATV plus 100 mM MVA diluted in PBS was injected into the left and right sides of the uteri at E5.5 (150 μl per side). Control mice were injected with 1% DMSO/PBS. At E10.5, the injected mice were sacrificed, and uteri and morphological changes in the embryos were examined under a light microscope.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.
Tips for asking effective questions
+ Description
Write a detailed description. Include all information that will help others answer your question including experimental processes, conditions, and relevant images.