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By measuring basal (no antibody) and maximally stimulated (4,600 pg/mL LPS) responses in the same blood sample, the EA of the test specimen is calculated by integrating chemiluminescence over time.
For this comparison, the intensity of SLI is obtained by normalizing the defocused 2D OTF and the total fluorescence intensity of TPLSM generated at a given z-plane for a uniform specimen is calculated by integrating the two photon intensity in each z section [ 30].
The LPS/anti-LPS complex primes the patient's neutrophils for an augmented response to stimulation with zymosan; by measuring basal (no antibody) and maximally stimulated (2,000 pg/ml LPS) responses in the same blood sample, the endotoxin activity of the test specimen is calculated by integrating chemiluminescence over time.
Substituting h with a function of r and ro gives: A h = π r 2 - r 2 - r o 2 3 = π 2 3 r 2 + 1 3 r o 2 Acortex_s (Area of the cortex of the section in a biopsied specimen) is calculated as: A cortex_s = L a + b × d b Where db is the internal diameter of the biopsy needle and La+b is "a + b" in Figure 5 for the total cortex length in biopsied specimens.
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(2) From the parameters, the hazard for each specimen was calculated and the specimen's survival curve was determined.
From the recorded pressure waves, stress, strain and particle velocity in the tested specimen were calculated.
The total amount of antibiotic eluted from each specimen was calculated by summing up data from all time points.
Therefore, the number of bands from each lane was counted and average number of bands per specimen was calculated (Table 3).
At the end of 6 h, the sample was removed from the cell and the amount of coulombs passed through the specimen was calculated.
The total current required for each specimen was calculated on the basis of the total steel surface area, using corrosion current density of 2.0 mA/cm2.0
Green's functions of the stress intensity factor and crack opening displacement of the CNB specimen are calculated in order to simulate the CL kinetics.
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