
- Tissue
- Peripheral blood
- Disease
- EBV-transformed B lymphoblastoid cell line (B-LCL); gastric cancer-associated donor
Documents
B-LCL-HROG17
Cell line · Product number 302112
B-LCL-HROG17 is a human Epstein-Barr virus (EBV)-transformed B lymphoblastoid cell line (B-LCL) derived from the peripheral blood of a 70-year-old Caucasi...
Customization / Recommendations
- B-LCL-HROG17Cell line€777.00
01General information
- Description
B-LCL-HROG17 is a human Epstein-Barr virus (EBV)-transformed B lymphoblastoid cell line (B-LCL) derived from the peripheral blood of a 70-year-old Caucasian male gastric cancer patient within the HROG biobank series. In vitro EBV transformation of primary peripheral blood B lymphocytes produced a stably immortalized, suspension-growing cell line. HROG17 cells display lymphoblast-like morphology and constitutively express EBV latency proteins and high-level HLA class I and II, co-stimulatory molecules CD80 and CD86, adhesion molecules CD54 and CD58, and B cell surface antigens CD19, CD20, and CD23, supporting potent antigen-presenting cell function.
B-LCL-HROG17 is employed in T cell and NK cell assays, HLA typing, mixed lymphocyte reactions, antigen presentation studies, and CTL protocols. As part of the HROG patient-matched biobank, it provides a defined immunological reference for gastric cancer immunological research. The 70-year-old male donor context is suitable for studies of age-related immune function in the context of gastric cancer, including analyses of T cell responsiveness and APC efficiency in older male patients.
- Tissue
- Peripheral blood
- Disease
- EBV-transformed B lymphoblastoid cell line (B-LCL); gastric cancer-associated donor
- Applications
- Immunology research; T cell and NK cell assays; HLA typing; antigen presentation studies; mixed lymphocyte reactions; CTL assay target cells; gastric cancer immunology
02Classification
- Organism
- Human
- Sex
- Male
- Growth properties
- Suspension
- GMO status
- GMO-S2
- GMO status details
- GMO-S2: This B-LCL contains a stably maintained EBV episome encoding viral latent-phase genes (EBNA-1/-2/-3, LMP-1/-2). EBV is classified as a risk group 2 pathogen. Handling requires BSL-2 containment. This classification applies within Germany; regulations may differ in other jurisdictions.
- Biosafety level
- 2
03Characteristics
- Morphology
- Lymphoblast-like
- Cell type
- B lymphoblast
- Doubling time
- 24 to 48 hours
04Identifiers
- Citation
- B-LCL-HROG17 (Cytion catalog number 302112)
- NCBI TaxID
- 9606
05Expression and susceptibility
- Viruses
- Transformant: EBV
06Handling and culture
- Culture medium
- RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a)
- Incubation atmosphere
37°C, 5% CO2, humidified atmosphere.
- Supplements
- Supplement the medium with 15–20% FBS
- Subculturing
- Dilute the culture to 2–5 × 10⁵ cells/ml with fresh pre-warmed complete medium every 2–3 days. Count viable cells before passaging to maintain optimal density. Do not allow cultures to exceed 2 × 10⁶ cells/ml. Centrifugation (300 × g, 5 min) may be used to exchange medium when needed. No enzymatic dissociation is required.
- Split ratio
- 1 to 4
- Seeding density
- 2 to 5 × 10⁵ cells/ml
- Fluid renewal
- Every 2 to 3 days
- 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 200 x g for 5 minutes, carefully discard the supernatant containing freezing medium.
Follow the procedure described under Post-Thaw Recovery
07Quality control and cryopreservation
- Freeze medium
- As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
- 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
- 70 years
- Ethnicity
- Caucasian
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.
- 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