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After 3 weeks of expansion in the presence of RAPA the beads were removed using a magnet and the cells counted.
Then magnetic beads were removed using a DynaMagTM-2 Magnet (Life Technologies).
The beads were removed using a magnetic holder and the remaining supernatant was used for selections.
After washing, IgG antibody-binding beads were removed by incubation with IgG-coated iron oxide particles, and the magnetized TentaGel beads were removed using a strong magnet.
Hit beads were removed using the magnetic pull-down method described above, with careful attention not to lose any of the isolated hits.
Beads were removed using a fritted plastic column and proteoliposomes were harvested by centrifugation for 30 min at 100,000 g, 4°C.
Similar(54)
Contaminating lymphocytes were removed using immunomagnetic beads as described previously (Kaspers et al, 1994).
Small fragments (<100 bp) were removed using AMPure Beads XP (Beckmann Coulter GmbH, Krefeld, Germany).
The small fragments (less than 100 bp) were removed using AMPure beads, and the supernatant contained the cDNA library.
Finally, the cDNAs shorter than 500 bp were removed using Ampure Beads according to the manufactures' instruction (Beckman, USA) before the preparation of the cDNA library.
The majority of proteins that could be labeled with biotin-maleimide were removed using activated thiol beads (lane 4).
More suggestions(15)
beads were prepared using
beads were sequenced using
beads were coated using
beads were synthesized using
beads were quantified using
beads were hardened using
beads were isolated using
beads were produced using
beads were imaged using
beads were inserted using
beads were washed using
beads were analyzed using
beads were read using
beads were constructed using
beads were counted using
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