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If no clear cell pellets were visible, samples were considered invalid for testing.
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To perform the shadow lookup at a visible sample, we do as follows.
For each visible sample, we project to the light space and then load each visible time range along with depth values to perform the shadow tests.
At a certain time, t, a sample H is visible to the camera and we need to load each visible sample of each triangle to perform the shadow tests.
Neither change of polymer electrolyte resistance nor visible sample dimensions were observed on stretching the film, having an initial cross-section of about 0.3×8 mm2 under the loads of 0.3 1.0 kg.
If the visible sample's time (t s ) is inside the visible time range [t 1, t 2 ], we find a depth value at t s using the linear interpolation along the depth range [z 1, z 2 ] and compare the interpolated depth with the sample's depth.
While GroEL1 was visible in samples purified from M. smegmatis mc155, the protein was noticeably absent in five out of six protein samples isolated from the groEL1ΔC strain.
This was not visible on samples which were prepared by polishing with cloths.
The cluster pattern was more visible when samples were coded by temperature departures (Fig. 2b).
A significant strand formation is visible in samples with a PC concentration of 2 mg ml−1 rather than at 0.2 mg ml−1.
Note that both OmpC and OmpF do not become soluble at 50°C and are therefore only visible in samples heated at 99°C [10].
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CEO of Professional Science Editing for Scientists @ prosciediting.com