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©2012 Baishideng Publishing Group Co.
World J Hepatol. May 27, 2012; 4(5): 176-183
Published online May 27, 2012. doi: 10.4254/wjh.v4.i5.176
Published online May 27, 2012. doi: 10.4254/wjh.v4.i5.176
Figure 3 Hepatocyte functionality before and after freezing.
Activity of the major cytochrome P450 enzymes; CYP1A2, CYP2C9, CYP3A7, CYP3A4, CYP2C19, CYP2D6 for the fresh hepatocytes (FRESH) compared to hepatocytes cryopreserved using either the STEM-CELLBANKER protocol (CB) or the standard dimethylsulfoxide in the University-of-Wisconsin solution protocol. The standard deviation exceeded the mean in many cases, illustrating the high within-groups variability. Data is presented as luminescence (LCU) per minute per DNA in nanograms. CYPs: Cytochrome P450 enzymes.
- Citation: Saliem M, Holm F, Tengzelius RB, Jorns C, Nilsson LM, Ericzon BG, Ellis E, Hovatta O. Improved cryopreservation of human hepatocytes using a new xeno free cryoprotectant solution. World J Hepatol 2012; 4(5): 176-183
- URL: https://www.wjgnet.com/1948-5182/full/v4/i5/176.htm
- DOI: https://dx.doi.org/10.4254/wjh.v4.i5.176