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. 2006 Oct 19;103(44):16496–16501. doi: 10.1073/pnas.0605835103

Fig. 1.

Fig. 1.

Inhibition of hemolysis by osmotic protection. (A) Hemolysis time courses were performed with or without 30 mM 10K-PEG. (B) Aliquots of supernatants from each time point in A were tested for protease-sensitivity of μ1. Arrowhead, trypsin-stable μ1 fragment. (C) Hemolysis reactions containing no PEG, 8K-PEG, or 10K-PEG were washed and resuspended in buffer with no PEG. (D) Hemolysis reactions were performed with PEGs of a range of sizes. Means ± SD of three experiments are shown.