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Free Radical Biol Med 2001;30:144061

Clin Genet

Homogenization was carried out in a Dounce homogenizer (~12 strokes per 10 ml of buffer per 11.5 g tissue)

BME- and PureCol EZ Gel-based 2D organoid culturing Transwell inserts (Thincerts, 12-well, pore size 0.4 m, Greiner Bio-One 665641) were coated overnight with 2% dilutions of BME (ref

So, if youve determined that you should regenerate your glutathione agarose beads before your next purification, what buffers should you use for this job