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Both the DB solution (10 mg/mL) and DO solution (10 mg/mL) were added in a series of increasing volumes (0.25, 0.50, 0.75, 1.0, 1.5 mL) to a series of five tubes, each containing the biomass sample and the buffer solution to create a 1 1 mixture of DO and DB dyes at increasing concentrations.
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Results were read 20 minutes after adding the buffer solution to the sera.
The dried lipids are solubilized in phosphate buffer solution to form a multilamellar vesicle (MLV) solution.
MMP2 was reconstituted in Hank's buffered saline solution (HBSS Life Technologiess) to create a 0.0002% by weight solution.
The sample sets were compared against a standard curve prepared from a 10 µmol mL−1 stock solution of p-NPP diluted in 0.1 M glycine buffer to create eight p-NPP standards ranging from dilutions of 1/5 1/640.
The dissolved sample was diluted 1 99 with heparinase digestion buffer to create a 0.03% (w/v) working crude heparin solution.
The easiest solution is to create logical cutoffs.
Menczer says the solution is to create a filter.
Callwell's solution tends to create a new problem, however.
A simple solution is to create a soakaway.
Brin said one solution is to create meat synthetically.
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