Objective: To discuss the method of isolating stem cell from adipose tissue. Methods: The subcutaneous adipose tissue from murine was digested, centrifugated, deodrythrocyted, etc and cultivated with DMEM/F12. The cultivation was exchanged once 2 days. Results: The cell spread fusiform shape, and proliferation with rapid rate. Conclusion: The cell from murine subcutaneous adipose tissue may be multipotential stem cell.