Human Ovarian Cancer-Associated Fibroblasts (CAFs) - Product Specifications
Quality Assurance & Characterization
Our Human Ovarian CAFs undergo rigorous quality control to ensure research reliability. The cells test negative for endothelial (von Willebrand Factor/Factor VIII), epithelial (cytokeratin 18), and smooth muscle (α-SMA) markers, confirming fibroblast purity. All cultures are certified free from microbial contamination (bacteria, yeast, fungi, and mycoplasma). The cells demonstrate positive expression of established CAF markers including FAP, PDGFR, Vimentin, PDPN, and CD70, maintaining stable growth characteristics for 3-5 passages when subcultured at recommended 1:2 to 1:3 ratios.
Research Applications
These primary ovarian CAFs are ideal for:
• Tumor microenvironment interaction studies
• Cell adhesion and invasion assays
• Molecular analysis (PCR, Western blot, immunoprecipitation)
• Cellular characterization (immunofluorescence, flow cytometry)
• Development of advanced 3D tumor models
• Drug screening and therapeutic development
Cell Handling Protocol
Shipping & Storage
Delivered in cryovials on dry ice
Optimal storage conditions:
Immediate culture initiation recommended
Alternative storage: liquid nitrogen vapor phase
Avoid -70°C storage (reduces cell viability)
Thawing & Culture Initiation
Rapidly thaw cells in 37°C water bath (≤2 minutes)
Surface sterilize vial with 70% ethanol
Remove cryoprotectant via centrifugation (125 × g, 5-10 min)
Resuspend in fresh CAF Growth Medium
Plate in AlphaBioCoat-treated T75 flask (6-8 mL coating solution, 15 min)
Maintain at 37°C with 5% CO₂ (pre-equilibrate medium 15 min)
Subculture Procedure
Remove spent medium and rinse with PBS
Add 2-3 mL Cell Detachment Solution (5-15 min incubation)
Neutralize with complete medium (6-8 mL)
Replate at 1:2 to 1:3 ratio in freshly coated flasks
Perform medium changes every 3-4 days
Cryopreservation
Use complete growth medium with 5% DMSO (Catalog #CGM5)
Store long-term in liquid nitrogen vapor phase