ask Ask a question
Favorite

SUnSET was performed as described (Ma et al., 2014). Hippocampal slices were incubated with puromycin (1 g/ml) for 60 min throughout the drug-treatment experiments. For the in vitro experiments, slices were treated with 100 pM GLP-1 (9-36). At the end of drug treatment slices were harvested and frozen on dry ice; protein lysates were prepared for Western blotting. Puromycin-labeled proteins were identified using the mouse monoclonal antibody 12D10 (1:10,000; Millipore). Protein synthesis levels were determined by taking total lane density in the molecular weight range of 10– 250 kDa.

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.

post Post a Question
0 Q&A