Sentence examples for measuring its absorbance from inspiring English sources
If the tyrosine or tryptophan content of the protein is known, therefore, the concentration of the protein solution can be determined by measuring its absorbance between 280 and 290 nanometres.
Quantitative analysis of Pyridine concentration was determined by measuring its absorbance using Shimadzu UV Visible spectrophotometer.
The superparamagnetic nanoparticles were separated by a magnetic separator and the clear supernatant containing the dissolved protein was used to find the enzyme concentration by measuring its absorbance at 280 nm.
The amount of solubilized curcumin was determined by measuring its absorbance at 425 nm with Synergy 2 Multi-Mode Microplate Reader (BioTek Instruments, Inc., Winooski, VT, USA) in comparison with calibration curve of curcumin in 90%% ethanol.
The supernatant liquids of the solutions of different concentrations were collected for the determination of concentrations for the remaining dye by measuring its absorbance (at λ max = 544 nm) with visible spectrophotometer (ELICO-207).
The supernatant liquid was collected and labeled for the determination of concentrations for the remained dye by measuring its absorbance (at λmax = 445 nm) with visible spectrophotometer (Elico, Model No. SL207).
Yellow colored solution confirmed the presence of AgNPs, and subsequently the solution diluted up to the volume mark with deionized water and measured its absorbance at 410 nm.
The aqueous phase was gently taken out to measure its absorbance at 600 nm.
The concentration of residual MB (i.e., supernatant liquid) was measured by its absorbance (A) at 665 nm with a Perkin-Elmer spectrophotometer.
Thereafter, 5 mL of concentrated sulfuric acid was added and the solution was left to cool for 15 min. Glucose was measured by its absorbance at 483 nm and expressed in terms of μg of glucose per g fresh weight of berry sample.
Subsequently, the protein-bound SRB in each well was solubilized with 200 μL of 10 mM Tris base solution (pH > 10) for 10 minutes on a plate shaker and measured for its absorbance at 510 nm with a FLUOstar OPTIMA plate reader (BMG LABTECH, Offenburg, Germany).
