The main focus of this protocol is to efficiently isolate viable primary glomeruli cultures with minimal contaminants for use in a variety of downstream applications. The isolated glomeruli retain structural relationships between component cell types and can be cultured ex vivo for a short time.
Rush, B. M., Small, S. A., Stolz, D. B., Tan, R. J. An Efficient Sieving Method to Isolate Intact Glomeruli from Adult Rat Kidney. J. Vis. Exp. (141), e58162, doi:10.3791/58162 (2018).