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The CryoAPEX Method for Electron Microscopy Analysis of Membrane Protein Localization Within Ultrastructurally-Preserved Cells
Published on: February 27, 2020
Development of a freeze-drying protocol for the long-term storage of S9-fraction at ambient temperatures
Sebastian Buchinger1, Elisabeth Campen, Eckard Helmers
1Department of Ecotoxicology and Biochemistry, Federal Institute of Hydrology (BfG), Am Mainzer Tor 1, 56068 Koblenz, Germany. buchinger@bafg.de
Abstract:
The purpose of this study was to investigate the long-term stabilization of the liver S9-fraction that is widely used in genotoxicity assays in order to mimic bio-activating processes of xenobiotics in vitro. A successful long-term stabilization of the S9-fraction meets the growing demand for the construction of a lab independent device for the detection of genotoxic compounds in field studies with an integrated module for the metabolic activation of pre-genotoxic compounds. The carbohydrates sucrose, trehalose and raffinose were tested in different concentrations or mixtures in order to increase the product stability of the S9-fraction during and after freeze-drying. The activity of the freeze-dried S9-samples was evaluated by means of their potential to activate pre-genotoxic compounds. The successful long-term stabilization of enzymes of the rodent liver S9-fraction for 6 weeks at room temperature by freeze-drying in the presence of 250 mM trehalose is presented.
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