Procell Logo
Search All
  • Search All
  • Cell Culture Media
  • Liquid Basal Media
  • Powder Basal Media
  • Complete Growth Media
  • Auxiliary Reagents
  • Balanced Salt Solutions
  • Growth Supplements
  • Antibiotics
Keyword cannot be empty !

SK-OV-3

Copy the product info.
Cat. No.: CL-0215 Publications(190)
SK-OV-3 - 1
  • SK-OV-3SK-OV-3 - 1
  • SK-OV-3SK-OV-3 - 2
  • SK-OV-3SK-OV-3 - 3
  • +2

CL-0215

$ 420.00

Select a size

1×10^6Cells/Vial×2Vials

Quantity

- +

In stock

Inquire

For order requirements and technical needs, please Contact Us

Product Introduction

General information
Cell Name SK-OV-3
Synonyms SKOV-3;SK.OV.3;SKOV3;Skov3;SKO3
Cellosaurus Accession CVCL_0532
Organism Human
Growth Properties Adherent
Morphology Epithelial-like
Disease ovarian cancer cells
Tissue Ovary; derived from metastatic site: ascites
Age 64Y
Sex Female
Instructions 1. Check all containers for leakage or breakage.
2. Remove the frozen cells from the dry ice packaging and immediately transfer them to liquid nitrogen (liquid or vapor phase) for long-term cryopreservation.
Complete Medium McCoy's 5A [PM150710]+10% Nutrient+1% Supplement
Incubation Atmosphere Air, 95%; CO₂, 5%
Temperature 37℃
Subcultivation Ratio 1:2-1:4
Medium Renewal 2 to 3 times per week
Dissociation Duration 2-3 min
Subculturing Procedure 1. Remove the culture medium from the T25 cell culture flask.
2. Add approximately 2 mL of PBS. Gently tilt the flask side to side until the PBS covers the entire bottom, then aspirate and discard the PBS.
3. Add 1 mL of 0.25% trypsin solution (containing EDTA). Gently tilt the flask side to side until the trypsin solution covers the entire bottom of the flask.
4. Incubate the cells at 37°C. Observe the cells under an inverted microscope and terminate digestion once the cells round up and detach. To avoid clumping, do not agitate the cells by tapping or shaking the flask during detachment.
5. Add 3 mL of complete culture medium to terminate digestion and disperse into a single cell suspension.
6. Collect the cell suspension and centrifuge at 1200 rpm (approximately 250 ×g) for 3 minutes. Carefully aspirate and discard the supernatant.
7. Add fresh complete culture medium, pipette gently several times to resuspend the cells, and seed them at the appropriate ratio into a new culture flask. Loosen the cap or use a vented cap for incubation.
Freeze Medium Freezing Medium (Serum-free & animal origin-free) [PB180438]
Storage Conditions For long-term cryopreservation, cryovials should be stored in liquid nitrogen at −150°C to −196°C. Storage at −80°C is restricted to short-term interim use only.
Background The SK-OV-3 cell line was established in 1973 by G. Trempe and L.J. Old from ascites of a patient with ovarian adenocarcinoma. SK-OV-3 cells are resistant to tumor necrosis factor (TNF) and several cytotoxic agents, including diphtheria toxin, cisplatin, and doxorubicin. The cells are tumorigenic in nude mice and form moderately differentiated adenocarcinomas consistent with primary ovarian carcinoma.
Tumorigenic Yes, in nude mice; forms moderately well differentiated adenocarcinoma consistent with ovarian primary.
Antigen Expression Blood Type B; Rh+
Gene Expression Blood Type B; Rh+
Biosafety Level BSL-1

Documents

Publications

CDCA5 promoted cell invasion and migration by activating TGF-β1 pathway in human ovarian cancer cells

Journal: Journal of Ovarian Research (2024) IF: 4

DOI: 10.1186/s13048-024-01393-5

Product Cited: Annexin V Binding Buffer (1×), SK-OV-3 Cells Line, Hey Cells Line, NIH:OVCAR-3 [OVCAR3] Cells Line, A2780 Cells Line, ES-2 Cells Line, HO-8910 Cells Line, IOSE-80 Cells Line

Home Contact Us Cart 1 My Order m_whatsapp
whatsapp