BeNa Culture Collection
|Culture medium||Special medium for HC11 cells: 88% 1640 + 10% FBS + 1% glutamine + 1% sodium pyruvate.|
|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|
|morphology||adherent, epithelial-like, irregularly shaped|
|Separation substrate||Chest; breast|
|application||An in vitro model for studying proliferation, signal transduction and differentiation of mammary epithelial cells.|
|Sharing mode||Public welfare sharing|
HC11 mouse mammary epithelial cells
adherent, epithelial cell-like
No. : 359449
Product format :2ml frozen vial x 2, or T25 flask x 1
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. 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 loss of cell viability.
Growth conditions: 37 ℃,5% CO2,88% 1640 + 10% FBS + 1% glutamine + 1% sodium pyruvate.
(1)1 new 100mm plate containing 12mL of the above culture solution;
(2) the frozen storage tube is taken out of liquid nitrogen or -80 ℃, bathed in water at 37 ℃ for 1~2min, and moved into the safety cabinet for resuscitation as soon as possible after complete dissolution;
(3) using a sterile straw to suck the dissolved liquid into the new plate and shake well clockwise;
(4) put in (37 ℃,5% CO2) in the incubator, change the liquid overnight, and it will be full in 3-5 days.
suck out the old culture solution. after PBS cleaning twice, add 2mL(/100mm dish/T25 bottle) of pancreatin (0.25% Trypsin + 0.02% EDTA) and observe under a microscope. during this period, it is forbidden to shake the culture dish. when the cells just fall off, suck out most of the pancreatin, leave about 0.5mL, move to the incubator for digestion, and take out about 2min. Subculture is terminated by digestion with 6mL of culture solution, and cells are gently blown evenly, and then passaged at 1:2. For cryopreservation, 3mL of cryopreservation solution (50% basic medium + 40% FBS + 10% DMSO) is used to terminate digestion, blow evenly, divide into 3 frozen storage tubes, freeze storage at -80 ℃ with a program cooling box, and transfer to liquid nitrogen storage overnight.
Recovery record: According to the recovery instructions, the results of the cell recovery are reported as follows:& nbsp;
|Item||quality standard||Recovery record|
|viability:||adherence is observed in 18 hours, the cell adherence rate ≥ 80.0% in 108hours||adherence is observed in 18 hours, the cell adherence rate ≥ 80.0% in 96hours|
|cell morphology:||Adherence, epithelial cell-like||Adherent, epithelial-like, irregular|
|Conclusion:||good viability, and no abnormal cell morphology, qualified|