Human liver cancer cells|BNCC359904 |BNCC

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Human liver cancer cells

Culture medium	RPMI-1640 complete medium: 90% RPMI-1640 + 10% FBS
Subculture procedure	Recovery steps: ① The frozen vial is taken out of liquid nitrogen or -80 ℃ refrigerator and put into PE gloves, quickly submersed into a 37 ℃ water bath pan, shaken The frozen vial to accelerate dissolution, and it is advisable to dissolve all within 1min; (2) Add the dissolved cell solution into a centrifuge tube containing 9ml of complete culture medium in an ultra-clean table, centrifuge at 1000-1200rpm for 5min, discard the supernatant, resuspend the cells with 1-2ml of complete media. (3) The cell suspension was added to T25 flask containing 5-6mL complete medium and cultured in an incubator. cell subculture: ① remove the medium, rinse twice with PBS, and add 1-2mL pancreatin (0.25% Trypsin + 0.02% EDTA); (2) Observe the digestion situation under the microscope. When the cell edge shrinks and the adherent is loose (a pipette can be used to suck up some pancreatin and gently blow somewhere in the cell layer, and the cell layer can be seen to detach with naked eyes, I .e. digestion is completed, otherwise digestion is continued). directly suck out pancreatin, add 5-6mL of complete medium, gently blow the cell layer off. (3) dispense the cell suspension into a fresh T25 flask as a ratio of 1:2, add appropriate complete culture medium, mix the cell suspension evenly, and culture in an incubator.; ④ Pay attention to the change of pH of medium and cell density, renew the medium regularly (2-3 times a week), and repeat the subculture or cryopreservation when the cell density reaches 80%-90%.
Growth conditions	Culture temperature 37 ℃; Atmosphere 5% CO2 + 95% air;
Growth characteristics	Adherent growth
Storage conditions	Liquid nitrogen
Type	Hepatocellular carcinoma cells
Safety level	2
morphology	Epithelial cell-like, short spindle-shaped, polygonal, irregular margin, monolayer adherent growth, clean background, no pigment, no vacuoles
Sharing mode	Public welfare sharing

SNU-449 human liver cancer cells

BNCC number: 359904

Growth properties : Adherent growth

Growth conditions: 37 ℃,5% CO₂

Complete medium: 90% RPMI-1640 + 10% FBS

Frozen storage conditions: 50% RPMI-1640 + 40% FBS + 10% DMSO

Receiving notice: if any abnormality is found on the day of receiving goods, please contact customer service within 24 hours. overdue goods will be deemed to be good! Freezing storage tube form: store in a refrigerator at -80 ℃ in time after receiving the goods. If it is not used for a long time, it should be transferred to liquid nitrogen overnight. During resuscitation, each tube shall not be retained once used up. T25 form: after receiving the goods, let it stand in the incubator for 2-3 hours, and then perform routine operation on the cells. Please strictly follow this instruction, otherwise no reissue service will be provided if cell inactivation is caused.

Recovery steps:
(1)The frozen vial is taken out of liquid nitrogen or -80 ℃ refrigerator and put into PE gloves, quickly submersed into a 37 ℃ water bath, shaken the frozen vial to accelerate dissolution, and it is advisable to dissolve all within 1min;
(2)Put the dissolved cell solution into a centrifuge tube containing 9ml of complete culture medium in an ultra-clean table, centrifuge at 1000-1200rpm for 5min, discard the supernatant, ?resuspend the cells with 1-2ml of complete media.
(3)The cell suspension was added to T25 flask containing 5-6ml complete medium and cultured in an incubator.

Subculture:
(1)remove the medium, rinse twice with PBS , and add 1-2mL pancreatin (0.25% Trypsin + 0.02% EDTA);
(2)Observe the digestion situation under the microscope. When the cell edge shrinks and the adherent is loose (a pasteur pipette can be used to suck up some pancreatin and gently blow somewhere in the cell layer, and the cell layer can be seen to detach with naked eyes, I .e. digestion is completed, otherwise digestion is continued), directly suck out pancreatin, add 5-6mL of complete medium, gently blow the cell layer off.
(3)dispense the cell suspension into a fresh T25 flask as the ratio of 1:2, add appropriate complete culture medium, make the cell suspension well distributed, and culture in an incubator.
(4)Pay attention to the change of pH value of media and cell density, renew the media regularly (2-3 times a week), and repeat the passage operation or cryopreservation when the cell density reaches 80%-90%.

Notes:
(1)The cells are density dependent. Initiate the subcultivation in T25 flask when the cell density reaches 80%; A subcultivation ratio of 1:2 is recommended.
(2)If the cells in sealed culture bottle, put it into the incubator for cultivation after handling, with the cap unscrewed.

Recovery record: according to the recovery requirements, the above cell lines were recovered, and the recorded results were as follows:

Item	quality standard	recovery record
viability:	adherence is observed in 18 hours, the cell adherence rate ≥ 80.0% in 96hours	adherence is observed in 18 hours, the cell adherence rate ≥ 80.0% in 88hours
cell morphology:	epithelioid cells	epithelioid cells, round, short spindle
attached figure:
Conclusion:	good viability, and no abnormal cell morphology, qualified

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