ask Ask a question
Favorite

The viability of neurons was measured by MTT assay. Briefly, the neurons (2,000 cells/well) were cultured in 96-well culture plates for 24 h. Then, MTT (5 mg/ml) was added into each well at 37°C for 4 h. After that, MTT was removed and 150 µl DMSO was added into the well to solubilize purple formazan. Then, absorbance at 570 nm was read using a microplate reader (PLUS 384; Molecular Devices, LLC). LDH cytotoxicity detection kit (cat. no. C0017; Beyotime Institute of Biotechnology) was used as previously described (22).

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