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A miniature quantity of sample was applied on slide and then observed under the microscope to test out nonflagellated amastigote, whereas in other parts buffer solution of pH 7.2 was mixed and placed in incubator for further process.
Samples were first eluted in 3-ml buffer solution of phosphate-buffered saline.
Buffer solution of pH = 2.0 containing 0.3 ?M oxytetracycline.
A buffer solution of phosphate with a pH 4 value was used in the experiments.
So, NaHCO3-Na2CO3 buffer solution of pH = 11.54 was chosen in the system.
It was standardized with a buffer solution of pH range between 4 and 9.
Accordingly, phosphate buffer solution of pH 3.4 was selected as the optimum carrier stream.
0.05 M Tris-HCl buffer solution of pH 7.4 and 8.2 were prepared.
To accelerate the PDLLA degradation, experiments were performed in alkaline buffer solution of pH 10.6.
So that, 1.0 mL of borate buffer solution of pH 10.5 and 1.5 mL of borate buffer solution of pH 9.0 were chosen as the optimum buffer volumes for Methods I and II, respectively.
The phosphate buffer solution of 4.2 pH was selected as the supporting electrolyte for the quantitative determination of DP.
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CEO of Professional Science Editing for Scientists @ prosciediting.com