Your English writing platform
Discover LudwigExact(1)
CSF, Cibacron Blue/Protein A gel slurry, and binding/wash buffer were mixed at 2 1 2 (v/v/v) ratio.
Similar(59)
300 ng of Cy5 and Cy3 labeled aRNA in 19 μl volume, 5 μl 10 × blocking agent and 1 μl 25 × fragmentation buffer were mixed together and incubated at 60°C for 30 min. Twenty-five microliters 2× GEx hybridization fuffer was added to each sample to stop the fragmentation reaction.
Tissue and buffer were mixed in a 1 20 relation.
Tissue and buffer were mixed in a 1 20 ratio.
Excess AlkA and 100 nM (final concentration) 19AεA or 19TεC DNA (in glycosylase assay buffer with no BSA) were mixed at 25 °C.
Blocking buffer (2.5% SDS, 20 mM MMTS in HEN buffer) was mixed with the samples and incubated for 30 min at 50°C to block free thiol groups.
Purified H2A and H2B were mixed at a 1 1 molar ratio in unfolding buffer, and the mixture was dialyzed against refolding buffer.
Briefly, 1 µl of 10× Fragmentation Buffer was mixed with 10 µl of DNA solution and incubated for 4 min at 95°C.
SDS-PAGE Sample Loading Buffer was mixed into the supernatant by proportion and the mixture was bathed for 5 min at boiling water.
The protein solutions were mixed at a 1 1 (v/v) ratio with the sample buffer (0.125 M Tris HCl, pH 6.8, 4% SDS, 20% glycerol).
DNA complexes were formed via a thermal annealing procedure: strands were mixed together at a 1 1 stoichiometry in TAE/Mg2+ buffer at a final concentration of 3 μM.
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