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The machine magnetizes a blood sample in water and sends a laser through it to detect malaria parasites in less than a minute.
Thermostability was estimated by incubating the enzyme sample in water bath at 30 70°C for 30 min.
The assay involves dissolving the sample in water and using a partial least squares model to predict the potency of the product.
Each tube was subsequently filled with 200 mL of each sample in water to produce the different concentrations of 0.30, 1.50, and 3.00 μg/mL.
Each Erlenmeyer flask was subsequently filled with 200 mL of each sample in water to produce a nominal pesticide concentration of 3.00 μg/mL.
Afterwards, LSPR extinction spectrum of the same sample in water was measured with the thin film substrate in water as reference.
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Porosity was determined by soaking the resin samples in water under vacuum.
Wet-conditioned samples were fabricated by immersing dry samples in water for 72 h.
The setup was optimized with carbon black samples in water and with various tryptophan concentrations at 281 nm excitations.
Here, we study a gentle oxidation of the interface by annealing buffer layer and monolayer graphene samples in water vapor.
The UV Visible absorption spectra of the samples in water were shown the characteristic polaron- π* and π−π* peaks.
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