HEK293-VEGFR2

Disclaimer: The prices displayed for cell lines are exclusively for academic/not-for-profit customers. For commercial entitites the price is approximately €6,250.
If you represent a commercial entity or are unsure which category applies, please contact us.

HEK293-VEGFR2 cells are human embryonic kidney 293 (HEK293) cells engineered to stably express human vascular endothelial growth factor receptor 2 (VEGFR2/KDR/Flk-1), a receptor tyrosine kinase that serves as a principal mediator of VEGF-driven angiogenic signaling. VEGFR2 is primarily expressed on endothelial cells and plays essential roles in vascular development, endothelial cell proliferation, migration, permeability, and survival through activation of downstream pathways including MAPK/ERK, PI3K/AKT, PLCγ, and SRC family signaling cascades. Dysregulated VEGFR2 signaling contributes to tumor angiogenesis, inflammatory vascular remodeling, and pathological neovascularization, making the receptor a major target in oncology and vascular disease therapeutics.

HEK293-VEGFR2 cells are widely used in angiogenesis research and drug discovery for characterization of VEGFR2-targeted monoclonal antibodies, tyrosine kinase inhibitors, ligand traps, bispecific antibodies, and anti-angiogenic biologics. The stable recombinant expression system supports quantitative evaluation of VEGF ligand binding, receptor phosphorylation, downstream signaling activation, receptor internalization, and inhibitor potency. These cells are also commonly employed in reporter assays, flow cytometry-based binding studies, kinase activity assays, and high-throughput therapeutic screening workflows. Because HEK293 cells support robust recombinant protein expression and efficient propagation, they provide a reliable platform for standardized VEGFR2 assay development and mechanistic signaling studies.

37°C, 5% CO₂, humidified atmosphere.

After thawing, split the cells at a ratio of 1:2 to 1:3 in T25 flasks and allow the cells to recover from the freezing process and to adhere for at least 24 hours.

For best attachment and viability after thawing the cells, we recommend using Collagen-coated flasks or plates for the initial seeding after cryo-recovery. Collagen coating is not required for subsequent routine culture of the cells.

1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

2. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.

3. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.

4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

5. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.

6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

7. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.

8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods.

To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections.

For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen.

Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage.

At Cytion, we stand behind the quality and viability of our products. We guarantee that our cells will be viable at the start of culture for 60 days after shipment from our facilities. We assure that all materials conform to the specifications described in the Certificate of Analysis and/or Product Sheet.

For full details, please refer to our Warranty Statement.