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Three new crystalline architectures based on acridinium trifluoromethanesulfonate salts [C13H10N]+[CF3SO3]– have been isolated as single crystals from the reaction of the dimeric hydroxo di-n-butylstannane trifluoromethanesulfonato complex [n-Bu2Sn(OH)(H2O)(CF3SO3)]2 (1) with acridine (C13H9N, Acr), in dichloromethane at room temperature.
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These tetra-perchlorates were isolated as single crystals and their structures were determined by X-ray diffractometry.
Ciliate species used in these experiments were isolated as single cells.
Fully grown immature oocytes were isolated as single cells by sieving through gauze several times.
Fully-grown immature oocytes were isolated as single cells by sieving through gauze several times in cold FSW.
Free oocytes were isolated as single cells by sieving through gauze several times followed by repeated rinsing and low speed (<1,000 rpm) sedimentation in cold filtered seawater.
Transformants from the yeast library pools were isolated as single colonies and their plasmids isolated.
The 12 evolved lines used in this study were isolated as single clones at generation 20,000, after which they have been stored in glycerol at -80°C.
All optically active amino acid derivatives were isolated as single regioisomers 5, and the given regioisomeric ratios were determined after the first step.
Thus, chiral-at-OsII iminopyridine chlorido and iodido complexes 1, 2, 3, and 4 were isolated as single crystals grown overnight at 277 K from a concentrated methanol solution.
In this research, rice (Oryza sativa L). was used as a model to develop a marker-genotyping system to meet the technical challenges, and the seed dormancy QTL SD 1-2, SD 7-1, and SD 12, which were isolated as single Mendelian factors into the same genetic background in the previous research, were selected to demonstrate the efficacy of the new genetic approach.
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