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The total quiescent current of the LDO including the current consumed by the reference buffer circuit is only 3.7µAA.
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All spectra shown at a specific temperature were constructed by subtracting the spectrum of the reference buffer solution without protein from the spectrum of the sample solution with protein.
Before being loaded into the cells, the sample (HSA or HSA-CTN) and the reference (buffer or buffer-CTN) solutions were degassed by stirring in an evacuated chamber at room temperature.
And the power consumption of the reference buffer is 17 mW from a 1.3 V power supply.
Reference spectra were recorded under identical conditions with only the reference buffer in the cell.
The final filtrate was used as the SV reference buffer.
Circular dichroism spectra were measured with a Jasco J-810 spectropolarimeter in a 1 mm quartz cuvette from 178 260 nm and data corresponded to an average of 10 15 repeated scans and subtracted by the reference spectrum of the buffer alone.
Samples spanning 0.1 1.5 OD at A230, A250, or A280 (Supporting Information, SI-Table 3) were prepared in a total volume of 500 μL by mixing concentrated protein solution with reference buffer to the desired final concentration for each experiment.
Reactions of NAMI-A, KP1339 and RuEDTA with NO were carried out in the reference phosphate buffer and analysed by absorption and FT-IR spectroscopies and by H-NMR.
The acquired spectra were corrected for minor solvent contributions by subtracting the reference spectrum of the buffer.
Signals from the reference surface and buffer blank injections were subtracted and the corrected results were globally fit to a 1 1 binding model.
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