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Thereafter, unique colony morphologies were selected with the aid of a binocular microscope and were serially passaged on ZM/10 or ONR7a agar until a single colony morphotype was achieved.
These morphologies were selected based on labeling method (intracellular dye injection) and reconstruction quality (400-µm sections were used and distal dendrites included in reconstruction) and files downloaded from Neuromorpho.org (cell IDs M. fascicularis: cnic_019 024 and cnic_055 060, M. mulatta: cnic_007 012 and cncic_050 054 (Duan et al. 2003)).
Similar(57)
Individuals from the three arthropod orders with the lowest percentage of matching Illumina MiSeq sequences to morphology were selected for further analysis.
Three flexible PU foams with similar morphology were selected for the study.
Petroleum coke graphite (PCG) and needle coke graphite (NCG) scraps with different aggregate and morphology were selected.
Colonies with the same morphology were selected for subculturing.
Colonies showing the predominant morphology were selected at random from each plate; isolates showing various colony morphologies were purified and screened for their phosphate-solubilizing ability.
At least 30 colonies of different morphology were selected arbitrarily and streaked consecutively at least four times to obtain pure colonies.
Then, five colonies for each morphology were selected and identified by negative COMBO22 microplate (Dade-Behring, MicroScan).
The two cell lines exhibiting the greatest extent of full-length Tim knockdown without changes in undifferentiated colony morphology were selected for further analysis.
Only the denuded oocytes with normal morphology were selected for further investigation.
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