MT-4 human acute lymphoblastic leukemia cells

BNCC number: 338052

Growth characteristics : Suspension growth

Growth conditions : 37 ℃,5% CO2

Complete medium : 90% RPMI-1640 + 20% FBS

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

Receiving notice: if any abnormality is found on the day of receipt, please contact the customer service within 24 hours. If it is overdue, it is deemed that the cells are well. For the frozen cells,  it shall be stored in the refrigerator at -80 ℃ upon arrival. If they are not used for a long time, they shall be transferred to liquid nitrogen for storage overnight.  Recovered cells in T25 culture flask, upon receipt, put the culture flask in the incubator for 2-3h, and then carry out handling procedure. Under sterile conditions, transfer the culture solution in T25 flask to a centrifuge tube, centrifuge at 1000-1200rpm/min for 5 ~ 10 minutes, resuspend the cells, transfer the suspended cells to a fresh T25 flask, add 10ml of complete medium, and put them into the incubator.Please operate in strict accordance with this instruction, otherwise the replacement of cells are not be available in case of loss of cell viability.

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.  
Cell subculturing: 
(1) Centrifugation: collect cells, centrifuge at 1000rpm for 5 minutes, discard the supernatant, add 1-2mL of culture solution and blow well, and dispense the cell suspension into a fresh T25 flask containing 8ml of culture medium according to a ratio of 1:2. 
(2) Half-volume solution exchange:  the culture flask is sit for 5-10 minutes, half of the supernatant medium is gently sucked away, the remaining medium with cell precipitation is resuspended and mixed evenly, and the cell suspension is dispensed into a fresh T25 flask containing 8ml of medium according to a ratio of 1:2. 
(3) 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 subculture or cryopreservation when the cell density reaches more than 2 × 10 to the sixth cells/ml.
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 instructions, the results of the cell recovery are reported as follows:

Item	quality standard	recovery record
viability:	the cell adherence rate ≥ 80.0% in 138hours	adherence rate ≥30.0% is observed in 18 hours,  the cell adherence rate ≥ 80.0% in 128hours
cell morphology:	suspension, lymphoblast	Suspension, lymphoblasts, round clusters
attached figure:
Conclusion:	good viability, and no abnormal cell morphology, qualified