Suggestions(1)
Exact(3)
DNA (ca. 10 ng) was placed into wells of 96-well plates and dried at room temperature over several hours.
RNA (500 ng) was placed in a 200 uL tube along with two uL of either Diluted Spike A or B and 1.2 uL of T7 Promoter Primer Mix.
A weighed quantity of a mixture of ATR and NG was placed in a mortar, and the mixture was kneaded thoroughly for 20 minutes with ethanol (1.5 times the amount of mixture).
Similar(57)
Two different concentrations of CCL21-vaults (200 ng and 600 ng), empty vaults (600 ng), and recombinant CCL21 (600 ng) were placed in the bottom chamber of a 24-well transwell plates and 2×105 T2 cells were added to the upper chamber.
A nasogastric (NG) tube was placed.
Nasogastric (NG) tube was placed by the bedside nurse under clean conditions after hand washing and appropriate measurements.
In all, 750 μl of BM±EGF (100 ng ml 1) was placed in the lower compartment to act as a potential attractant.
A hybridization mix containing 5 ng probe was placed on each sample and incubated overnight at 37°C in a moist chamber.
Powdered NG (1 g) was placed in a 15 mL tube.
Briefly, 500 ng of RNA was placed into a 20 μL reaction volume containing 0.2 μM of each primer, 10 μL of Syber Green I RT-PCR one-step master mix, and 0.2 μL of reverse transcriptase.
For the T7 endonuclease I assay, 10 μL of 1× NEB2 reaction buffer (New England BioLabs, Japan Inc). containing 200 400 ng of PCR product was placed in a 0.2-mL PCR tube (QSP #430-Q; Thermo Scientific).
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com