Exact(20)
Cells were treated with SLT-VEGF (0.1 10 nM), and cell viability, proliferation, and endothelial tube formation were assessed.
After 4 h, cells were treated, and the transfection efficiency of GFP-LC3, as well as the effect of the different treatments on punctae formation, were assessed by fluorescence microscopy after 16 and 24 h (Olympus, Aartselaar, Belgium).
Kinetics of CDC formation were assessed using three SiC laser pyrolysis-produced nanopowders of different average size.
Spermatozoa were incubated in the different media (0, 1 and 2 h) and sperm motion parameters, lipid membrane disorder, plasma membrane integrity and reactive oxygen species (ROS) formation were assessed.
Radiographic features of OA severity, joint space narrowing (JSN), a surrogate for cartilage loss and osteophyte (OST) formation, were assessed for the knee and ankle.
Effects of MWCNT and TCC on radical formation were assessed by measuring intracellular ROS in RTL-W1, T47Dluc, and H295R cells.
Similar(40)
(c) Secondary mineral formation was assessed for the subhumid (Catalina conifer forest) site.
8 10 days later, colony formation was assessed and the survival fraction determined for each treatment.
Indel formation was assessed by comparing gel band density for germline vs specifically cleaved bands.
ROS formation was assessed on a plate reader (excitation 485 nm, emission 535 nm) at the indicated time-points.
ROS formation was assessed on a plate reader (Ex 485 nm/Em 535 nm) at 8 (A) and 12 h (B).
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