Human gastric cancer cells|BNCC339570 |BNCC

Essential Information Certificate Related Products

Human gastric cancer cells

Culture medium	IMDM complete medium: 90% IMDM + 10% FBS
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 all within 1 minute; (2) Add the dissolved cell solution to 9ml & nbsp in the ultra-clean table; In a centrifuge tube with complete culture medium, centrifuge at 1000-1200rpm/min for 3-5 minutes, discard the supernatant, resuspend the cells with 1-2ml of complete media. ③The cell suspension was then added to the T25 flask containing 6-8mL of complete medium and placed in an incubator for culture. Cell subculturing: ① transfer the cell suspension solution into a centrifuge tube, centrifuge for 5 minutes at 1000RPM to collect cells; (2) rinse T25 flask twice with PBS, add 1-2mL pancreatin (0.25% Trypsin + 0.02% EDTA); 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 on the cell layer, the cell layer can be seen to detach with the naked eye, that is, digestion is completed, otherwise digestion is continued), directly suck out pancreatin, add 5-6ml of complete medium, gently blow the cell layer off. (3) The cells obtained from the above two steps are evenly mixed and then dispensed into fresh T25 flasks as a ratio of 1:2. add appropriate complete medium, mix the cell suspension evenly, and culture in an incubator. ④ Pay attention to the change of PH value and cell density of the culture medium, change the liquid regularly (2-3 times a week), and repeat the passage operation or cryopreservation when the cell density reaches 80%-90%.
Growth conditions	Culture temperature 37 ℃; Atmosphere 5% CO2 + 95% air;
Growth characteristics	semi-adherent and semi-suspension growth
Storage conditions	Liquid nitrogen
Safety level	1
morphology	In CM4-culture medium, semi-adherent and semi-suspended, epithelial cell-like, round
Separation substrate	Organ: Gastric disease: Gastric cancer, metastatic lesions: pleural effusion; clavicle and axillary lymph nodes and Douglas's depression
application	On the cheek pouch of hamsters treated with antithymocyte serum. No, it's a nude mouse
Sharing mode	Public welfare sharing

KATOⅢ human gastric cancer cells

Semi-adherent semi-suspended, epithelial cell-like

No. 339570

Product format: 2ml frozen vial x 2, or T25 flask x 1

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

Growth Condition:37 ℃,5% CO₂ CM4-1 culture solution

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 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 lose of cell viability.

Growth conditions:37 ℃,5% CO₂,CM4-1 culture solution. CM4-1 culture solution: 90% IMDM-H + 10% FBS. IMDM:IMDM culture solution.

Recovery steps:

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

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.

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

(3)Put it into incubator (37℃，5%CO₂）, change the media overnight, and it will grow up in 7-8 days.

Subculture/ cryopreservation:

The culture medium (including suspended cells) was sucked into the centrifuge tube for centrifugation (110g, 3min) and cells were collected；rinse twice with PBS, add 2ml of 0.25%Trypsin+0.02%EDTA, do not shake the culture dish during the period. Observed under the microscope, remove most of the trypsin(with 0.5ml left) when the cells detach. transfer it to the incubator for digestion about 1minute, and take it out.

(1)Subculture: The digestion of the above dish cells was terminated with 4mL CM4-1 culture medium, and the centrifuge tube cells were suspended with 2ml CM4-1 culture medium. A total of 6mL culture medium was sucked into the dish and mixed, and the culture was divided into 3-6 dishes.

(2)Cryopreservation: terminate 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	quality standard
viability	adherence is observed in 12hours, the cell adherence rate ≥ 80.0% in 90hours	adherence is observed in 18 hours, the cell adherence rate ≥ 80.0% in 90hours
cell morphology	adherent, epithelial cell-like	in CM1-1 culture solution, adherent, epithelial cell-like, polygonal, spindle
attached figure
conclusion	good viability, and no abnormal cell morphology, qualified