BeNa Culture Collection
info@bncc.com
| Culture medium | BNCC395877 |
| Description | |
| Composition | |
| Growth conditions | 28 ℃; 100% air; |
| Subculture procedure | Resuscitation steps: ① Remove the frozen vial from liquid nitrogen or -80 ℃ refrigerator and place it in PE gloves. Quickly immerse it in a 37 ℃ water bath, shake the vial to accelerate dissolution, and dissolve it completely within 1 minute; ② Add the dissolved cell solution into a centrifuge tube containing 9mL of complete medium on a ultra-clean bench, centrifuge at 1000-1200rpm for 5 minutes, discard the supernatant, and resuspend the cells in 1-2mL of complete medium. ③ Add the cell suspension into a T25 flask containing 5-6mL of complete medium and place the flask in an incubator. Cell passage: ① Use a 5ml pipette to directly aspirate the culture medium and blow the cells; ② Observe under the microscope whether the cells are evenly dispersed. ③ Divide the cell suspension into fresh T25 flasks at a ratio of 1:2, add appropriate complete culture medium, mix the cell suspension evenly, and culture it in the incubator.; ④ Pay attention to changes in the pH value of the culture medium and cell density, change the medium regularly (2-3 times a week), and repeat the passage operation or cryopreservation when the cell density reaches 80% -90%. |
| morphology | Epithelial-like,Round,Monolayer adherent growth |
| Sharing mode | Public welfare sharing |
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