Your English writing platform
Discover LudwigSuggestions(1)
Exact(1)
Following emulsion PCR, DNA bound beads were isolated and sequenced using long-read (LR) sequencing kits.
Similar(11)
Beads with displacements less than 5 nm (limitation of resolution detection) and loosely bound beads were not selected for analysis.
These conjugates were homogenised mechanically and native Jurkat plasma membrane fragments bound to the magnetic beads were isolated.
Afterward, the beads were isolated and the supernatant discarded.
About 100 beads were isolated.
Samples were washed five times with lysis buffer after which, RNA bound to beads was isolated using Trizol LS according to manufacturer's instructions with the following modifications: after RNA precipitation, RNA was DNase treated for 30 min at 37°C and then extracted with Acid:Phenol CHCl3 (Ambion) before a second precipitation with 100% Ethanol.
Antibody bound proteins were isolated on protein A agarose beads (RepliGen, Waltham, CA) or protein A magnetic Dynabeads (Invitrogen, Carlsbad, CA), washed extensively, eluted, and cross-links reversed according to the Upstate protocol.
Following standard in-gel digestion, the phosphorylated peptides from α-casein bound to the VIPing reagent were isolated using solid-phase streptavidin beads and subjected to LC MS/MS analysis.
The HMW-MAA-positive cells were isolated using immunomagnetic beads.
Thirty-five beadisplayinging a bright red halo were isolated.
Monocytes were isolated from cells not bound to the anti-CD3 column, by repeating the process above with anti-CD14 mAb-coated beads.
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