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L5178-R
Tissue
Thymus
Disease
Leukemia
Synonyms
L5178Y-R, L5178YR, L-5178-Y-R, LY-R, LYR

Documents

L5178-R

Cell line · Product number 400258

The L5178-R cell line is a murine lymphoma cell line derived from mouse lymphoid tissues. This cell line is particularly notable for its use in studying t...

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01General information

Description

The L5178-R cell line is a murine lymphoma cell line derived from mouse lymphoid tissues. This cell line is particularly notable for its use in studying the mechanisms of lymphomagenesis and the cellular responses to various treatments, including chemotherapeutic agents and radiation. L5178-R cells are radioresistant, which makes them a valuable model for exploring the molecular and genetic factors that contribute to radiation resistance in cancer cells. This attribute is essential for research into improving therapeutic strategies for treating resistant forms of cancer.

L5178-R cells are also frequently employed in mutagenesis and carcinogenesis studies due to their high sensitivity to mutagenic agents. This sensitivity is exploited in assays that assess the mutagenic potential of chemical compounds, contributing to toxicological research and safety evaluations. The cell line's genetic and phenotypic characteristics provide a robust platform for in vitro studies, enabling scientists to dissect the pathways involved in cancer development and progression. Additionally, the L5178-R cell line is used in immunological research to understand the interaction between tumor cells and the immune system, aiding in the development of immunotherapeutic approaches.

Tissue
Thymus
Disease
Leukemia
Synonyms
  • L5178Y-R
  • L5178YR
  • L-5178-Y-R
  • LY-R
  • LYR

02Classification

Organism
Mouse
Growth properties
Suspension
Biosafety level
1

03Characteristics

Morphology
Round cells
Cell type
T lymphocyte
Tumourigenic
In DBA/2 mice

04Identifiers

Citation
L5178-R (Cytion catalog number 400258)
NCBI TaxID
10090
Cellosaurus
CVCL_4234

05Expression and susceptibility

Viruses
MAP-test negative: Sendai, Ektromelie, Polyoma, K-Virus, Kilham, Reo 3, PVM, LCM, M.pulmonis, MVM, Theiler's GD VII, Toolan's H-1, MHV, LDV, RCV/SDA, M-Adenovirus, B.piliformis.

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 10% FBS, 1 mM sodium pyruvate, 1% NEAA
Subculturing
Maintain cultures by periodically adding or replacing the medium. Initiate cultures with a density of 5 x 105 cells/ml and keep the cell concentration within the range of 3 x 105 to 1 x 106 cells/ml for optimal growth.
Seeding density
1 x 106 cells/ml
Fluid renewal
Every 3 days
Post-thaw recovery
2 to 4 days
Thawing and culturing
  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.

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

Breed / subspecies
DBA/2