How To Use Buffer solution In A Sentence
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The kit comprises the following main components: buffer solution, reduced coenzyme, pyruvic acid, adenosine triphosphate, pyruvate oxidase, pyruvate carboxylase, malic dehydrogenase and a stabilizer.
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Conclusion Citrate buffer solution is the best solution for the preparation of povidone-iodine gel and the solution is helpful to improve the stability of the gel.
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An additional 34 ml buffer solution was added and the sample was then ultracentrifuged at 100,000 × # for 4 h.
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Excess solution was removed and fresh degassed buffer solution was added to the sample and allowed to incubate for 30-60 min before imaging.
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The transiting phase was modulated by 0.1 M of citrate buffer solution, sodium octyl sulphonate, methanol, and EDTA-Na.
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Excess unfused vesicles were removed by exchanging the solution in the cell with buffer solution several times after cooling the sample down to room temperature.
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Experiments were performed in a liquid sample cell containing two silica spheres immersed in a buffer solution and evanescently coupled to the same single-mode, near-infrared optical fiber.
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To fill the channels with the aqueous buffer solution, the hydrophobic surface of PDMS was wetted with ethanol, which was gradually replaced by water.
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The kit comprises the following main components: buffer solution, reduced coenzyme, pyruvic acid, manganese chloride, pyruvate oxidase, oxaloacetic decarboxylase, malic dehydrogenase and a stabilizer.
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Close to the sphere surface, the oligonucleotide interacts with the evanescent field of the WGM, which extends about a wavelength into the buffer solution.
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Spectra are corrected for the wavelength dependence of the emission monochromator and the photomultiplier and also by subtracting background intensities of the buffer solution.
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The kit comprises the following main components: buffer solution, coenzyme, pyruvic acid, glycerophosphoric acid, glycerol-3-phosphate oxidase, glycerol-3-phosphate dehydrogenase and a stabilizer.
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The kit comprises the following main components: buffer solution, reduced coenzyme, oxaloacetic acid, acetyl coenzyme A, phosphoenolpyruvate carboxylase, pyruvate dehydrogenase and a stabilizer.
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The buffer solutions used were 0.01 M sodium phosphate at pH 7, with 0.02% sodium azide added as a bactericide.
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The contents were then discarded, the wells were washed with the wash buffer solution and blotted on a paper towel.
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A spectral change was observed upon addition of lipid vesicles to the buffer solution of the sensitizers.
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We switched to individual aliquots of buffer solution, prepared in single-use tubes.
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Monoliths doped with azurin were prepared adding the protein to the buffer solution to be mixed with the sol.
