Microchamber slide design for cell confinement during imaging- Tetrahymena rostrata timelapse data
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We performed Imaging on a Nikon Ti2-E & Yokogawa CSU W1-SoRa microscope. The microscope was equipped with an ORCA-Fusion BT digital C-MOS camera. We used a 10× 0.45 Plan Apo Air or a Plan Apo λD 100x OIL OFN25 DIC N2 objective for differential interference contrast (DIC) imaging. More microscopy information is detailed in the metadata file associated with each .nd2 file.
Tetrahymena rostrata was provided by Andrzej Kaczanowski, who isolated the cells from the small snail Cohlicopa lubrica near Warsaw. The cells were cultured in medium consisting 0.5% yeast extract and 0.5% of proteose peptone supplemented with 250 ug/ml streptomycin sulphate and 250 ug/ml penicillin G to maintain sterility.
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References
- Kaczanowski A, Brunk CF, Kazubski SL. Cohesion of Clonal Life History, Senescence and Rejuvenation Induced by Autogamy of the Histophagous Ciliate Tetrahymena rostrata. Protist. 2016 Nov;167(5):490-510. doi: 10.1016/j.protis.2016.08.003. Epub 2016 Aug 26. PMID: 27631279.
- Avasthi P, Garcia III G, York R. (2022). Microchamber slide design for cell confinement during imaging. https://doi.org/10.57844/arcadia-z6hb-fs28