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The deposits were further washed with water and centrifuged twice.
The RBCs were further washed with PBS three times.
The dyed samples were further washed and soaped using 1 gpl non-ionic surfactant solution.
The beads were further washed using a buffer containing 10 mmol/L imidazole until no traces of the protein were detected in the flow-through.
The organics were further washed with a saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and concentrated in vacuo.
The products were further washed with ethanol and water for several times, dried under vacuum at room temperature, and labeled as Ag-ZnO/HNTs.
To eliminate the impurity ions, the products were further washed with deionized water for several times and then dried in air at 60°C.
Centrifugation (9000 rpm) was performed for 20 min to collect hardened microspheres which were further washed three times with purified water for 5 min each.
The particles were further washed with ethanol for three times to remove the unreacted chemicals and then dispersed in 60 mL ethanol.
Prior to dissolution, the sample was stuck upside down on copper tape to flatten the remaining structures, which were further washed with deionized water for several times to completely remove the residue of NaOH.
The cells were further washed twice.
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CEO of Professional Science Editing for Scientists @ prosciediting.com