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Please read the guidelines before participating in this community.
It is important to use sterile sample containers, even for non-biological experiments. Otherwise bacteria can create a biofilm which can clog the FluidFM cantilever and interfere in your experiments.
Use sterilized consumables (e.g. plates and dishes). In the case of non-sterile consumables, they should be sterilized for example by autoclaving them. As an alternative, you can properly clean them with ethanol.
A good cleaning protocol for FluidFM experiments is described below (from Guillaume-Gentil et al., 2014):
1. Clean dishes with 2-propanol.
2. Rinse them with filtered ddH2O.
3. Dry them with a nitrogen stream.
4. Plasma-treat them for 2 min.
5. The dish is now ready for FluidFM experiments.
Guillaume-Gentil, O., Zambelli, T. & Vorholt, J. (2014). Isolation of single mammalian cells from adherent cultures by fluidic force microscopy. Lab on a Chip, 14 (2), 402-414. doi: 10.1039/c3lc51174j
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Collaboration to improve CRISPR-based multiplexed gene editing.
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|Asked: 3/20/19, 11:08 AM|
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|Last updated: 6/15/20, 5:33 AM|