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In-line capturing allowed us to normalize the 2D7 binding responses for different receptor capture levels.
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Although different binding responses were observed for the three cellulase fusions, they were all attached to the scaffold.
Native and recombinant frutalin yielded different binding responses in the prostate tissues due to their differences in carbohydrate-binding affinities.
The binding responses were corrected for buffer effects by subtracting responses from a blank flow cell.
Instead, we obtained informative DNA duplex stability prior by assuming different binding preferences for different TFs.
Moreover, the binding responses were similar to values obtained for the interacting proteins, indicating that the binding affinity was not affected by the fusion.
It has multiple binding sites, accounting for different functions.
The binding responses (RU) have been reference subtracted and normalized for clarity.
Plasma was examined for viremia, antigen specific IgG, IgA and IgM binding responses and neutralizing antibodies.
Bindings provide support for different kinds of communication protocols.
Light response curves for different leaf segments.
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