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Other synthesis components were obtained as follows: Sterile vials were obtained from Hollister-Stier; Millex filters were from Millipore; QMA-light and Oasis HLB 1 cc cartridges were purchased from Waters.
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GMP-grade DOTA-NOC acetate in 60 μg vials was obtained from ABX (Radeberg, Germany).
Ketamine (100 mg/mL vial) was obtained from Phoenix Pharmaceutical (St. Joseph, MO) and administered in combination with xylazine (20 mg/mL vial) acquired from Hospira (Lake Forest, IL).
Human blood from healthy donors in EDTA-vials was obtained from the Austrian Red Cross, Vienna.
Vials of microspheres were obtained by convenience sampling, either before or after extraction of the desired treatment activity.
HPLC vials and caps were obtained from Anachem.
All cells, except those in p+11b, originally came from the same cryogenic vial; those in p+11b were obtained from a second vial of frozen cells in order to check whether there were differences between the same passage numbers from different vials (p+11a vs. p+11b).
The cytotoxic drugs used in the assay were obtained as vials for injection and made up according to manufacturers' instructions.
Mitomycin C (Kyowa, London, UK) and Gemcitabine (Eli Lilly, Basingstoke, UK) were obtained as vials for injection, and made up according to the manufacturer's instructions.
Although no formal testing was performed on the bupivacaine or lidocaine used, successful regional anesthetics were obtained using vials from the same lot on other patients during the same time period.
An average of 13.3 ± 7.3 ml/day was phlebotomized after day 21, and 3.8 ± 1.5 vials of blood/patient per day were obtained.
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CEO of Professional Science Editing for Scientists @ prosciediting.com