human endometrial adenocarcinoma cells 

  KLE

BNCC number : 101009

growth properties : adherent growth culture conditions: 37 ℃,5% CO₂

complete medium : 90% DMEM-H/F12 + 10% FBS. DMEM-H/F12:DMEM high sugar culture solution mixed with F12 culture solution 1:1

cryopreservation conditions: 50% basal medium + 40% FBS + 10% DMSO

Receiving notice:  if any abnormality is found on the day of receiving goods, please contact customer service within 24 hours. if it is overdue, it will be deemed as good receiving goods. Frozen storage tube form, after receiving the goods in a refrigerator at -80 ℃ for storage. 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, the culture bottle shall be placed in the incubator for rest for 2-3h, and then the cells shall be subjected to routine operation. 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 3-5min, 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 instructions, the results of the cell recovery are reported as follows:
 

item	quality standard	Recovery record
Viability:	adherence is observed in 18 hours, the cell adherence rate ≥ 80.0% in 110 hours	adherence is observed in 18 hours, the cell adherence rate ≥ 80.0% in 96 hours
cell morphology:	epithelial cell-like	Epithelial cell-like, irregular
attached figure:
Conclusion:	good viability, no abnormal cell morphology, qualified