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High-fidelity finite-element analyses were carried out on ten welded connection specimens between the square steel tube column and H-beam flange under monotonic tensile loading.
The environmental transfer of specimens between the FIB/SEM (used for specimen processing) and the LEAP (used for analysis) is facilitated via a docking flange and an environmental transfer shuttle (Fig. 1d, e).
No significant differences at the 0.05 significance level were encountered in the analysis of 10 clinical serum specimens between the multiplexed immunoassay and a commercially available enzyme-linked immunosorbent assay (ELISA).
No significant difference at the 0.05 significance level was encountered in the analysis of 6clinical serum specimens and 6spiked blank new born cattle serum specimens between the developed immunoassay and commercially available electrochemiluminescent (ECL) method for the detection ofCEA.
a CAD-rendered image of the ETH isolated from the local electrode atom probe (LEAP) with the various main parts as (1) main vacuum chamber hub, (2) docking port for specimen transfer shuttle (shown connected), (3) high-temperature ambient pressure reactor chamber, (4) manipulator transfer specimens between the ETH and the LEAP.
Using the SMCS model and VGM as fracture criteria, the post-fracture load displacement curves of eighteen notched round bar specimens and two welded connection specimens (between the square steel tube column and H-beam flange) that fractured at different locations were traced by deleting the failure elements one by one.
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The length of each specimen between the jaws of the machine (Torsee's Scopper type-OS-100) was maintained at 10 cm (0.5 g).
Jute fibres were cut into equal pieces, 30 cm in length, and the length of each specimen between the jaws was maintained at 10 cm.
This preload was applied to assure proper but gentle fixation on top surface of the specimen between the load cell and the tip (d) of the pushing rod.
For museum records, we estimated daily encounter rates by counting all specimens collected between the first and last date of a particular collection series.
The mean expression level of most candidate Suppressive miRNAs in the clinical specimens was between the corresponding miRNA values in the PAG and HAG cells, except for miR-185 and miR-31.
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