MWexperimental | 186 | kDa |
MWexpected | 186 | kDa |
VPorod | 2900 | nm3 |
log I(s)
1.04×10-1
1.04×10-2
1.04×10-3
1.04×10-4
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s, nm-1
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Synchrotron SAXS data from solutions of Japanese encephalitis virus 3' UTR RNA in 10 mM Bis-tris, 100 mM NaCl, 15 mM KCl 15 mM MgCl2, 10% glycerol, pH 5 were collected on the B21 beam line at the Diamond Light Source (Didcot, UK) using a Eiger 4M detector at a sample-detector distance of 3.7 m and at a wavelength of λ = 0.094 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A sample at 1.1 mg/ml was injected onto a Shodex 403KW-4F HPLC column at 15°C using a flow rate of 0.16 ml/min. Seven successive 3 second frames were collected through the SEC elution peak of the sample (from a total of 600 SEC-SAXS data frames). The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
Sample injection volume = UNKNOWN. |
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