Jurkat细胞
低温保存
活力测定
细胞培养
细胞生物学
细胞
化学
生物
生物物理学
生物化学
免疫学
T细胞
胚胎
免疫系统
遗传学
作者
Emma Buick,Andrew Mead,Abeer Alhubaysh,Patricia Bou Assi,Parijat Das,James Dayus,Mark C. Turner,Lukasz Kowalski,Jenny Murray,Derek Renshaw,Sébastien Farnaud
标识
DOI:10.1089/bio.2023.0100
摘要
Cell culture is a critical platform for numerous research and industrial processes. However, methods for transporting cells are largely limited to cryopreservation, which is logistically challenging, requires the use of potentially cytotoxic cryopreservatives, and can result in poor cell recovery. Development of a transport media that can be used at ambient temperatures would alleviate these issues. In this study, we describe a novel transportation medium for mammalian cells. Five commonly used cell lines, (HEK293, CHO, HepG2, K562, and Jurkat) were successfully shipped and stored for a minimum of 72 hours and up to 96 hours at ambient temperature, after which, cells were recovered into standard culture conditions. Viability (%) and cell numbers, were examined, before, following the transport/storage period and following the recovery period. In all experiments, cell numbers returned to pretransport/storage concentration within 24-48 hours recovery. Imaging data indicated that HepG2 cells were fully adherent and had established typical growth morphology following 48 hours recovery, which was not seen in cells recovered from cryopreservation. Following recovery, Jurkat cells that had been subjected to a 96 hours transport/storage period, demonstrated a 1.93-fold increase compared with the starting cell number with >95% cell viability. We conclude that CellShip
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