1
Discover top-quality products tailored for scientific and medical research. Request a personalized quote today
to enhance your projects.
| Product Code | OAW59M; OAW 59M; 59 M |
| Species | Human |
| Cat.No | ABC-TC0016 |
| Product Category | Tumor Cell Lines |
| Size/Quantity | 1 vial |
| Cell Type | Epithelial |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Ovary |
| Disease | Ovarian Serous Adenocarinoma |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Human Ovarian Cancer Cell Lines |
Human ovarian tumour epithelial. Derived from a patient with carcinoma of the ovary and is of ascitic fluid origin.
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $100 coupon. Simply click here and submit your paper’s PubMed ID (PMID).
For research use only
P30/OHK (NC)
59M
The percentage of CD45 expression in 59M Cell Line was detected by flow cytometry to be approximately 65.6%.
The recommended seeding density for 59M cells can vary depending on the specific experimental needs and growth characteristics. As a general guideline:
Initial Seeding Density: Start with a seeding density of around 5,000 to 10,000 cells per square centimeter (cells/cm²) of growth area. Adjust based on the growth rate and experimental requirements.
Recommended Culture Medium and Conditions for 59M Cells:
Culture Medium: 59M cells are typically cultured in RPMI-1640 medium supplemented with fetal bovine serum (FBS), usually at a concentration of 10% to 20%. Antibiotics such as penicillin-streptomycin are commonly added to prevent contamination.
Temperature and Atmosphere: Maintain the cells at 37°C in a humidified atmosphere containing 5% CO₂. This environment helps to mimic physiological conditions and supports cell growth.
Poor Cell Attachment: Ensure that culture vessels are properly coated with extracellular matrix proteins (e.g., collagen, fibronectin) before seeding. Also, avoid over-trypsinization during passaging, as excessive trypsin can damage cell membranes and affect attachment.
Slow Growth or Reduced Viability: Check the freshness and quality of the medium and FBS used. Serum should be heat-inactivated to minimize the risk of viral contamination. Ensure that cells are not over-confluent and are regularly subcultured to maintain active growth.
Contamination: Maintain strict aseptic techniques, including frequent cleaning of the work area and equipment. Use antibiotics judiciously to prevent bacterial or fungal contamination.
pH Imbalance: Monitor the pH of the medium regularly and adjust if necessary to maintain optimal conditions for cell growth (typically pH 7.2-7.4).
Cryopreservation and Thawing of 59M Cells:
Cryopreservation:
Preparation: Use a freezing medium containing RPMI-1640 supplemented with 10-20% FBS and 10% dimethyl sulfoxide (DMSO). DMSO helps prevent ice crystal formation during freezing, which can damage cells.
Freezing Protocol:
Harvest cells during exponential growth phase.
Resuspend cells in the freezing medium at a concentration of 1-2 million cells per mL.
Transfer aliquots of the cell suspension to cryovials.
Place cryovials in a controlled-rate freezer or a -80°C freezer for slow freezing.
Transfer cryovials to liquid nitrogen for long-term storage (below -130°C).
Thawing:
Thawing Protocol:
Quickly thaw cryovials in a 37°C water bath until only a small ice crystal remains.
Transfer the cell suspension to a tube containing pre-warmed RPMI-1640 medium with FBS (10-20%).
Centrifuge cells at low speed to pellet them, remove the supernatant, and resuspend cells in fresh medium.
Plate cells in culture vessels pre-coated with appropriate matrix proteins and incubate in a 37°C, 5% CO₂ atmosphere.
