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We first characterized its membrane behavior, and then used absorbance measurements to study its lateral distribution in model membranes.
We used absorbance (optical density) at 260 nm to quantify the cRNA concentrations, and absorbance at 550 nm and 650 nm to measure the efficiency of Cy 3 and Cy 5 dye incorporation.
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Protein concentrations were measured using absorbance at 280 nm.
Binding of Py biotin to avidin was studied using absorbance and fluorescence spectroscopic techniques.
Using absorbance intensities at 5176 cm− 1, the conversion and kinetic behaviors of the esterification reaction were estimated.
It was proposed to describe degradation effect using absorbance change, and prediction model of pesticide residues degradation was obtained according to the relationship between degradation time and absorbance.
Briefly, thawed stocks were centrifuged at high speed (5 min, 15000 g) and their protein content determined using absorbance at 280 nm using a NanoDrop 1000 spectrophotometer (Thermo Scientific, UK).
The effect of acetic acid (AA) concentration on the films optical parameters was studied by using absorbance and transmittance data recorded during ultraviolet-visible (UV Vis) spectroscopy.
Band-gap evaluation was performed using absorbance spectra of coatings and showed considerable decrease of band-gap energy in the presence of CNTs.
First, a two-level full factorial design was performed that included the following chemical variables: hydrochloric acid concentration, tetrahydroborate concentration, sulfanilamide concentration and tetrahydroborate volume, using absorbance as the response.
Determination of sample color was done using absorbance reading and standard curve relating absorbance and CU.
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