BeNa Culture Collection

Human B- cell lymphoma cells-BNCC
Human B- cell lymphoma cells-BNCC
  • Human B- cell lymphoma cells-BNCC
  • Human B- cell lymphoma cells-BNCC
  • Human B- cell lymphoma cells-BNCC
【SU-DHL-4】

Human B- cell lymphoma cells

  • Price: $373
  • number:BNCC358289
  • Form:
    Lymphoblastoid, rounded, irregular margin, single cell, clean background, no pigment, no vacuoles
Basic package DNA extraction
Package:
  • Package A:STR report + 2 vials of frozen cell
  • Package B:STR report + 2 vials of frozen cell + 100ml of complete medium
Essential Information Certificate Related Products
Human B- cell lymphoma cells
Culture medium RPMI-1640 complete medium: 90% RPMI-1640 + 10% FBS
Subculture procedure Recovery steps: ① Take out the frozen vial from liquid nitrogen or -80 ℃ refrigerator and put it into PE gloves, quickly submerse into a 37 ℃ water bath, shake 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 3-5min, discard the supernatant, resuspend the cells with 1-2ml of complete media. ③The cell suspension was then added to the T25 flask containing 6-7mL of complete medium and placed in an incubator for culture. The culture flask is recommended to be cultured uprightly. cell subculture: ① centrifugation: collect cells, centrifuge at 1000rpm for 5min, 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 medium exchange method: half-volume medium exchange method can be selected; Please gently suck half of the supernatant culture medium, resuspend and mix the remaining culture medium with cell precipitation, and divide the cell suspension into a fresh T25 flask containing 8mL culture medium according to a ratio of 1:2. (3) 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 more than 2 × 106 cells/ml.
Growth conditions Culture temperature 37 ℃; Atmosphere 5% CO2 + 95% air;
Growth characteristics Suspension growth
Storage conditions Liquid nitrogen
Type Suspension growth
Safety level 1
morphology Lymphoblastoid, rounded, irregular margin, single cell, clean background, no pigment, no vacuoles
Separation substrate Aged 38-year-old race white male with ascites
Sharing mode Public welfare sharing

SU-DHL-4 human B cell lymphoma cell

suspension, lymphoblast-like

No. 358289

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

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.  Centrifuge tube 15mL, after receiving the original centrifuge tube placed in the incubator for 4 hours, then perform routine operations on the cells. 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% CO2,90% RPMI-1640 + 10% 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 3-5 days.

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 120hours inoculation with 20% cell solution,  suspension growth rate reaches  30.0% in 18 hours, and 80.0% in 110hours
cell morphology: suspension, lymphoblast-like suspended, lymphoblast-like, round
attached figure:
Conclusion: good viability, and no abnormal cell morphology, qualified

 

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