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The USML intensity depends on kinds of ML material, input intensity of ultrasonic wave and so on.
The goal of the present investigation was to visualize the propagating crack in a mechano-luminescence (ML) material to enable the measurement of instantaneous R-curves and directly observe the bridging (shielding) stress in a fast-propagating crack system.
A 50 μl aliquot of the extracted DNA from the biopsy samples and a 10 μl aliquot of the extracted DNA from the LBC samples (i.e., approximately 10% of the original 1 ml material, equal to the suggested input for the Roche Linear Array (LA) test (Roche Molecular Systems, Inc., Branchburg, NJ, USA)) was used for the PCR reaction stage of the Roche LA test.
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First, it was hypothesized that the 80 ml contrast material had penetrated into the alveolar interstitial compartment and had created a gas contrast material interface.
The mean DNA yield (μg) per ml sampled material with the new version was 91.1 μg/ml (95% CI 77.8-104.4), and that of material sampled with the earlier version was 90.4 μg/ml (95% CI 83.2-97.5) per sample (Table 2).
The In0.4Ga0.6As QD layers were grown by the deposition of 8.5 ML of material.
600 µL buffer (100 mM TrisCl, 150 mM NaCl, 1 mM EDTA, 0.1% Triton X-100, 0.05% SDS, 10% glycerol, 5 mM DTT, 1x Complete Protease inhibitor) were added to 0.5 mL ground material and vortexed thoroughly.
Briefly, the process involved 1 mL of material aliquoted and pelleted for centrifugation at 13,000 r.p.m.
1.0 mL hydrogel material was injected in each disc of mimic group.
50 μl of antibody-coupled beads were added to each 1 ml chromatin material instead of 100 μl.
A total of 0.9 ml contrast material and 0.1 ml mepivacaine hydrochloride 1% were mixed and injected intradermally into the upper-outer periareolar areas [ 17].
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