BeNa Culture Collection
info@bncc.com
| Culture medium | BNCC338068 |
| Description | DMEM-H Complete Medium (with 10% FBS) |
| Composition | 90%DMEM-H+10%FBS |
| Growth conditions | 37°C; 5% CO₂ + 95% air |
| Subculture procedure | Recovery steps: ① Remove the cryovial from liquid nitrogen or -80 ℃ freezer and place it in PE gloves. Quickly immerse it in a 37 ℃ water bath and shake the cryovial to accelerate dissolution. It is recommended to dissolve it completely within 1 minute; ② Add the dissolved cell solution into a centrifuge tube containing 9mL of complete culture medium on a super clean bench, centrifuge at 1000-1200rpm for 5 minutes, discard the supernatant, and resuspend the cells in 1-2mL of complete culture medium. ③ Then add the cell suspension to a T25 bottle containing 6-8mL of complete culture medium and culture it in an incubator.Cell passage: ① Gently scrape off the adherent cells with a cell scraper, transfer them along with the culture medium to a centrifuge tube, centrifuge at 1000 RPM for 5-8 minutes, and discard the supernatant; ② Add 1-2 mL of complete culture medium to the cell pellet collected from suspended cells and adherent cells, and mix well; ③ Add culture medium at a rate of 5-6mL/bottle, and divide the cell suspension into culture bottles containing 5-6mL of culture medium at a ratio of 1:2; ④ Pay attention to changes in the pH value of the culture medium and cell density, change the medium regularly (2-3 times a week), and repeat the passage operation or cryopreservation when the cell density reaches 80% -90%. |
| morphology | Lymphoblast-like,Spindle-shaped (short),Round,irregular edge |
| Sharing mode | Public welfare sharing |
Super Tube(Super Tube)
BNCC100297
Y79(Y79)
BNCC100707
bEnd.3[BEND3](bEnd.3[BEND3])
BNCC337672
MC38(MC38)
BNCC337716
MH7A(MH7A)
BNCC337864
MADB106(MADB106)
BNCC339574