22Rv1 人前列腺癌细胞 |
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点击次数:1178 更新时间:2017-01-17 |
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22Rv1 人前列腺癌细胞说明书 General Information: Organism: | Homo sapiens, human | Tissue: | prostate | Culture Properties: | adherent | Morphology: | epithelial |
Culture Method: Complete Growth Medium: | RPMI-1640(Gibco31800-022)+10%FBS+ Penicillin/Streptomycin | Subculturing: | Volumes are given for a 25cm2 flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes. - Remove and discard culture medium.
- Briefly rinse the cell layer with 0.25%(w/v) Trypsin-EDTA solution to remove all traces of serum that contains trypsin inhibitor.
- Add 1.0 to 2.0mL of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed. Discard Trypsin-EDTA solution.
- Add 6.0 to 8.0mL of complete growth medium and aspirate cells by gently pipetting.
- Add appropriate aliquots of the cell suspension to new culture vessels.
- Incubate cultures at 37°C, 5% CO2.
| Subc*tion Ratio: | A subc*tion ratio of 1:3 to 1:6 is recommended | Cryopreservation: | Freeze medium: Complete growth medium supplemented with 10% (v/v) DMSO Storage temperature: liquid nitrogen vapor phase |
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