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LN229-Luc
Tissue
Brain, right frontal parieto-occipital cortex
Disease
Glioblastoma
Synonyms
LN 229, LN229, LNT-229

Documents

LN229-Luc

Cell line · Product number 305692

LN229-Luc is a bioluminescent derivative of the human LN229 glioblastoma cell line, engineered to stably express a firefly luciferase reporter gene. The p...

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Lot
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  • CoA
1

01General information

Description

LN229-Luc is a bioluminescent derivative of the human LN229 glioblastoma cell line, engineered to stably express a firefly luciferase reporter gene. The parental LN229 cell line was established from a glioblastoma of the right frontal parieto-occipital cortex in a 60-year-old female patient and is widely used as a preclinical model of glioblastoma multiforme (GBM). LN229 cells exhibit epithelial morphology and harbor key molecular alterations characteristic of glioblastoma, including PTEN loss and activation of the PI3K/AKT signaling pathway, while retaining wild-type EGFR status. These features make LN229 a valuable model for studying GBM pathogenesis, signaling pathway dependencies, and responses to targeted and cytotoxic therapies.

The stable luciferase integration in LN229-Luc enables sensitive, noninvasive bioluminescence imaging (BLI) of tumor burden in orthotopic intracranial and subcutaneous xenograft models in immunocompromised hosts. The emitted luminescent signal correlates with viable tumor cell number, supporting longitudinal monitoring of tumor engraftment, intracranial growth, and therapeutic response without repeated invasive procedures. LN229-Luc is particularly suited for evaluating blood-brain barrier-penetrant agents, temozolomide combinations, targeted PI3K/mTOR inhibitors, and immunotherapy approaches in preclinical GBM research.

LN229-Luc retains the established biological and molecular properties of the parental LN229 line, providing a relevant platform for glioblastoma drug development and mechanistic studies. The luciferase reporter substantially enhances experimental sensitivity and enables real-time longitudinal pharmacodynamic assessment of treatment efficacy in live animal models. Researchers should validate luciferase activity, growth kinetics, and molecular phenotype under their specific experimental conditions prior to large-scale preclinical use.

Tissue
Brain, right frontal parieto-occipital cortex
Disease
Glioblastoma
Synonyms
  • LN 229
  • LN229
  • LNT-229

02Classification

Organism
Human
Sex
Female
Growth properties
Adherent
GMO status
GMO-S1
GMO status details
GMO-S1: This cell line contains a stably integrated firefly luciferase reporter cassette (Luc2, codon-optimized) introduced via replication-incompetent lentiviral transduction. The resulting polyclonal cell population was maintained under puromycin selection (1–5 µg/mL). S1 containment is required. This classification applies only within Germany and may differ elsewhere.
Biosafety level
1

03Characteristics

Morphology
Epithelial

04Identifiers

Citation
LN229-Luc (Cytion catalog number 305692)
NCBI TaxID
9606
Cellosaurus
CVCL_0393

05Expression and susceptibility

Protein expression
Luc
Antigen expression
Luc2 (firefly, codon-optimized)

06Handling and culture

Culture medium
DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a)
Incubation atmosphere

37°C, 5% CO2, humidified atmosphere.

Supplements
Supplement the medium with 10% FBS
Dissociation reagent
Accutase
Subculturing
Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium.
Split ratio
1 to 3
Seeding density
2-4*10^4/cm²
Fluid renewal
2 to 3 times per week
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 200 x g for 5 minutes, carefully discard the supernatant containing freezing medium.

  7. 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
60 years
Ethnicity
European

10Product details

Composition table