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Thus shape complementarity in addition to electrostatic attraction is required for very tight binding as previously concluded from a study of chemical modification of Ocr [15].
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Thus, as previously concluded, a higher total delay average is expectable.
This result is consistent with rate-limiting chemistry with this substrate, as previously concluded.
As we previously concluded, VB5 is not variable, having a low VF (0.37).
A comparison by Curtis and Mnzava (2000) had previously concluded that ITNs were at least as efficacious as IRS.
The resulting plasma membranes were suspended in binding buffer and used in [35S]GTPγS binding assay as previously described [11].
The results were analysed assuming a one-to-one binding model as previously described [27].
RNA binding by recombinant NS5B RNA polymerase was determined using a filter-binding assay as previously described [26].
As mentioned previously, we concluded that the test-retest reliability analysis was of low quality according to the COSMIN checklist.
The interaction as a sum of intercalation and groove binding modes was concluded.
The antigen-binding properties (immunoreactivity) of 211At-BR96 relatove to BR96 were analyzed by determination of the equilibrium binding constant (K d) by saturation binding curve analysis as previously described [18], using BN7005 cells as the target antigen.
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