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The humidity test was performed by placing 1 g of specimen powder in six calibrated porcelain capsules, which were warmed at 105°C for 4 h and then weighed.
One vacuum sample (0.55 g of specimen) from the feeder part of machine no. 10 had 2.9x10 CFU of B. anthracis, equal to 5.5x10 CFU of B. anthracis per gram of sample material.
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Equal amounts, of approximately 6 g, of each specimen were subjected to cell isolation either by tissue digestion or by explant technique.
However, SCC-50 and SCC-100 specimen were cast in only one layer at four different positions from section E through G of the specimens, as shown in Fig. 4b.
Based on Howard's chart, a particle size, smaller than 2 mm, requires 20 g of saturated sample specimen [24].
The k EDTA is defined as the rate constant of the dissolution of 0.1 g of an Fe0 specimen in 50 mL of a 2 mM M EDTA solution for 96 h (4 days).
From the initial and final weight of the metal specimen, the rate of corrosion was determined using the following equation upsilon = frac{KW}{DSt}, (1 where υ corrosion rate (mm year−1), W weight loss (g), S surface area of metal specimen (cm2), t time of treatment (h), D density of specimen (g cm−3) and K a constant (8.76 × 104).
{text{Mass loss}};left( % right) = frac{W - C}{C} times 100 (3)where C is the conditioned weight of the specimen (g), and W is the weight of specimen after immersion (g).
g, Scatter plot of specimens for bgPC1 versus bgPC2, with convex hulls for all groups, except H. floresiensis and H. luzonensis.
Tissue samples of approximately 0.1 g were collected immediately after resection of specimen.
For MACS, a minimum of 0.5 g tissue specimen was required.
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