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. Author manuscript; available in PMC: 2008 Oct 1.
Published in final edited form as: Arch Biochem Biophys. 2007 Jul 14;466(1):31–39. doi: 10.1016/j.abb.2007.07.001

Table 1.

Sedimentation coefficients and molecular mass of PDO as determined by Analytical ultracentrifugation.

Conditionsa Detection method Loading concentration (signal units) s20,W, S (± 0.2 S) Mass, kDa (± 10 kDa) PDO oligomer sizeb
Low salt Interference 3.40 11.78 363 7.3
Low salt Absorbance at 405 nm 0.12 11.99 372 7.6
Low salt Absorbance at 455 nm 0.16 11.99 387 7.9
High salt Interference 0.39 11.50 318 6.5
High salt Absorbance at 280 nm 0.34 11.81 283 5.8
High salt Interference 0.92 11.37 301 6.1
High salt Absorbance at 280 nm 0.72 11.66 284 5.8
a

Buffer for low salt was 20 mM KPO4, pH 6.9; for high salt, 50 mM KPO4, 0.5 MKCl, pH 7. Buffers contained 5 mM phthalate.

b

Based on monomer mass of 49 kDa.