
- Tissue
- Ovary
- Disease
- Chinese hamster ovary, non-neoplastic; genetically engineered for IL2RA (CD25) surface expression
Documents
CHO-IL2RA
Cell line · Product number 305980
Disclaimer: The prices displayed for cell lines are exclusively for academic/not-for-profit customers. For commercial entitites the pr...
Customization / Recommendations
- CHO-IL2RACell line€1,900.00
01General information
- Description
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.
CHO-IL2RA cells are recombinant Chinese hamster ovary (CHO) cells engineered to stably express human interleukin-2 receptor alpha (IL-2Rα; CD25/IL2RA), a high-affinity cytokine receptor subunit involved in regulation of T-cell activation and immune homeostasis. CD25 forms part of the heterotrimeric IL-2 receptor complex together with IL-2Rβ (CD122) and the common gamma chain (CD132), enabling high-affinity binding of interleukin-2 and activation of downstream JAK/STAT signaling pathways. Physiologically, CD25 is highly expressed on activated T lymphocytes and regulatory T cells (Tregs), and aberrant expression has also been reported in several hematologic malignancies and inflammatory disorders.
CHO-IL2RA cells are widely used in immunology and therapeutic development workflows for characterization of anti-CD25 monoclonal antibodies, cytokine-based therapeutics, bispecific antibodies, and engineered immune cell targeting strategies. The stable recombinant expression system enables quantitative assessment of ligand binding, receptor occupancy, antibody affinity, and receptor internalization. These cells are also valuable for flow cytometry assay development, potency testing, cell-based binding assays, and high-throughput screening applications involving IL-2 pathway modulation. In addition, CHO-IL2RA models can support studies examining selective targeting of activated T cells or regulatory T-cell-associated mechanisms in autoimmunity, transplantation, and cancer immunotherapy.
- Tissue
- Ovary
- Disease
- Chinese hamster ovary, non-neoplastic; genetically engineered for IL2RA (CD25) surface expression
- Applications
- Antibody screening; IL2RA-targeted therapy development; T-cell biology research; autoimmune disease research; flow cytometry
02Classification
- Organism
- Chinese hamster
- Sex
- Female
- Growth properties
- Adherent and suspension
- GMO status
- GMO-S1
- GMO status details
- GMO-S1: This CHO cell line contains an IL2RA expression cassette supporting receptor-function analyses. This classification applies only within Germany and may differ elsewhere.
- Biosafety level
- 1
03Characteristics
- Morphology
- Epithelial-like
- Cell type
- Epithelial cells
- Doubling time
- approx. 14-16 hours
04Identifiers
- Citation
- CHO-IL2RA (Cytion catalog number 305980)
- NCBI TaxID
- 10029
- Cellosaurus
- CVCL_A8W8
05Expression and susceptibility
- Surface antigens
- IL2RA (CD25)
06Handling and culture
- Culture medium
For adherent cultures: DMEM:Ham's F12 (1:1), w: 3.1 g/L Glucose, w: 2.5 mM L-Glutamine, w: 15 mM HEPES, w: 0.5 mM Sodium pyruvate, w: 1.2 g/L NaHCO3 (Cytion article number 820400a)
For suspension cultures: CHO Growth Medium A (from InSCREENeX; InSCREENeX catalog number INS-ME-1039)
- Supplements
- For adherent cultures: Supplement the medium with 5% FBS. Add Geneticin (G418-Sulfat) to achieve a final concentration of 0.5 mg/mL.
- Dissociation reagent
- For adherent cultures: Trypsin-EDTA
- Subculturing
- For routine adherent cell culture: Aspirate the old culture medium from the adherent cells, and wash them with PBS to remove any remaining medium. After aspirating the PBS, add the appropriate volume of Trypsin/EDTA solution based on the culture vessel size (e.g., 1 ml for a T25 flask, 3 ml for a T75 flask) and incubate at room temperature or 37°C for 5-10 minutes, or until the cells detach. Monitor detachment under a microscope, and gently tap the vessel if necessary to release the cells. Once detached, add complete medium to inactivate the Trypsin/EDTA, gently resuspend the cells, and transfer an aliquot of the cell suspension into a new culture vessel containing fresh medium. Place the vessel in an incubator set to 37°C with 5% CO2, and change the medium every 2-3 days.
- Split ratio
- 1 to 5
- Seeding density
- 2 to 5 x 104 cells/cm2
- Fluid renewal
- 2 to 3 times per week
- Post-thaw recovery
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 adherent cultures) for at least 24 hours.
- Thawing and culturing
Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.
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.
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.
Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.
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.
Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.
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.
Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.
07Quality control and cryopreservation
- Sterility
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.
- Freeze medium
- As a cryopreservation medium, we use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
- Storage conditions
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.
- Shipping conditions
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.
08Donor
- Donor age
- Adult
09Legal and safety
- Safety precautions
- When planning to store a cryovial in liquid nitrogen for future thawing, it is mandatory to adhere to stringent safety measures. Appropriate protective gloves and clothing are essential, and the use of a face mask or safety goggles is required during the transfer of frozen samples to or from the liquid nitrogen tank. This is to mitigate the risk of injury from potential cryovial explosions upon removal, which can result in the projection of sharp fragments.
- Disclaimer
- Our cells are provided for in vitro laboratory research purposes exclusively and are not intended for clinical or diagnostic use, nor are they to be administered to humans or used for veterinary purposes. Users must adhere to all applicable guidelines and regulations for the handling and use of these cells in a research setting.
- Warranty
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.
- Third-party agreements apply
- Yes


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