Human acute T-lymphocytic leukemia cells|BNCC338495 |BNCC

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Human acute T-lymphocytic leukemia cells

Culture medium	Jurkat special culture solution: 84% RPMI-1640 15% FBS 1% Gln
Subculture procedure	Recovery steps: ① Take out the frozen vial from liquid nitrogen or -80 ℃ and put it into PE gloves, quickly submerse into a 37 ℃ water bath pot, shake the frozen vial to accelerate dissolution, and it is advisable to dissolve it completely within 1 minute; (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/min for 3-5 minutes, discard the supernatant, resuspend the cells with 1-2ml of complete media minutes ③The cell suspension was then added to a T25 flask containing 6-8mL complete medium and placed in an incubator for upright cultivation. Cell subculturing: ① Centrifugation: collect cells, centrifuge at 1000rpm for 5 minutes, discard the supernatant, resuspend the cells with 1-2ml of complete medium, 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 method: after the culture flask is allowed to stand 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 × 106 cells/ml.
Growth conditions	37 ℃;5% CO2 95% air;
Growth characteristics	Suspension growth
Storage conditions	Liquid nitrogen
Safety level	1
morphology	Lymphoblast-like, rounded, neatly edged, few clubby, clean background, no vacuoles
Separation substrate	Peripheral blood derived from a 14-year-old man with T-lymphocytic leukemia
Sharing mode	Public welfare sharing

Jurkat human acute T lymphocyte leukemia cells

suspension, lymphoblast-like

No. : 338495

culture :37 ℃,5% CO₂ CM12-1 liquid medium

product format : 2ml frozen vial x 2, or 15mL centrifuge tube

Biosafety level : 1, handle in ultra-clean table or safety cabinet

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. Cells in centrifuge tube, upon receipt, put the culture flask in the incubator for 4h, and then carry out handling procedure. During recovery, each vial shall be used up once and shall not be retained. After recovery, the cells can be passed on to the next generation and can be used normally. Please operate in strict accordance with this instruction, otherwise the replacement of cells are not be available in case of loss of cell viability.

culture conditions :37 ℃,5% CO₂,CM12-1 culture solution. CM12-1 culture solution: 85% RPMI-1640 + 15% FBS. RPMI-1640:1640 culture solution, containing glutamine.

Recovery steps:

(1)prepare a new 100mm culture dish containing 12ml of the above culture medium;

(2)remove the frozen vial from liquid nitrogen or refrigerator at -80℃, thaw the vial in 37°C water bath for 1-2 minutes. Transfer the vial to biosafety cabinet for culture as soon as the contents are completely thawed.

(3)draw the solution with a sterile pipette, drip into a new culture dish, and mix it evenly by shaking clockwise;

(4)Put it into incubator (37℃，5%CO2）, change the media overnight, and it will grow up in 5-7 days.

Subculture: the suspended cells were gently blowed and evenly distributed into 3-6 fresh culture medium dishes. After being shaken well, the cells were put into the incubator for culture

Cryopreservation: The suspended cells were transferred to the centrifuge tube for (110g, 3min) centrifugation，after centrifugationterminate digestion with 3ml of cryopreservation solution （90%FBS+10%DMSO), aspirate and dispense into 3 frozen vials, and cryopreserve at -80 ℃ with a programmed cooling box.

Recovery record: According to the recovery instructions, the results of the cell recovery are reported as follows:

item	quality standard	recovery record
viability	suspension growth rate ≥ 80.0% in 120 hours	inoculation with 20% cell solution, suspension growth rate reaches 40.0% in 18 hours, and 80.0% in 108 hours
cell morphology	suspension, lymphoblast-like	In the CM12-1 culture medium, suspended, lymphoblast-like, most of them grow in groups
attached figure
Conclusion:	good viability, no abnormal cell morphology, qualified