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The pH values of all buffer solutions were controlled by a pH meter.
The pH values of all buffer solutions were controlled by pH-meter.
The radiometal, ligand, and buffer solutions were controlled to mix in the chip with different volume ratio using LabVIEW interface software.
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The pH of the phosphate and acetate buffer solutions was controlled by a digital pH metre (InoLab pH/ion, WTW GmbH & Co. KG, www.wtw.com) calibrated at 25 °C with standard buffers of pH 7.0 and 4.0 (WTW GmbH & Co. KG, www.wtw.com).
The pH of the buffer solutions was controlled by a digital pH meter (InoLab pH/ion, WTW GmbH & Co. KG, www.wtw.com) calibrated at 25 °C with standard buffers of pH 7.0 and 4.0 (WTW GmbH & Co. KG, www.wtw.com).
The pH of the solution was controlled using buffer solution.
Octanol and buffer solutions were presaturated.
The homogeneous application of trypsin by a spraying device can overcome this problem if spraying conditions such as flow rate, distance and buffer solution are carefully controlled.
The combined solution was maintained at room temperature for 30 min. The same volume of buffer solution was added to the control samples without Fe2+ or 64-nucleotide hairpin DNA.
Buffer solution was used as a negative control and 10 mg/mL histamine dihydrochloride (ALK-Abello, Hørsholm, Denmark) was used as positive control concurrently with SPT.
For comparison purposes, a HEPES buffer solution was used as a negative control with a recorded PT value of 14.5 s, and a 0.7 IU/mL heparin solution was used as a positive control, with a recorded PT value of >60 s.
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