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LN229-Luc
Vev
Brain, right frontal parieto-occipital cortex
Sykdom
Glioblastoma
Synonymer
LN 229, LN229, LNT-229

Dokumenter

LN229-Luc

Cell line · Produktnummer 305692

LN229-Luc er et bioluminescerende derivat av den humane glioblastomcellelinjen LN229, som er genetisk modifisert til å uttrykke et reportergen for ildflue-luciferase på en stabil måte. Den p...

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01Generell informasjon

Beskrivelse

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.

Vev
Brain, right frontal parieto-occipital cortex
Sykdom
Glioblastoma
Synonymer
  • LN 229
  • LN229
  • LNT-229

02Klassifisering

Organisme
Menneske
Sex
Kvinne
Vekstegenskaper
Tilhenger
GMO-status
GMO-S1
Detaljer om GMO-status
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.
Biosikkerhetsnivå
1

03Egenskaper

Morfologi
Epithelial

04Identifikatorer

Kildehenvisning
LN229-Luc (Cytion catalog number 305692)
NCBI-skattenummer
9606
Cellosaurus
CVCL_0393

05Uttrykk og mottakelighet

Proteinekspresjon
Luc
Antigenuttrykk
Luc2 (firefly, codon-optimized)

06Håndtering og kultur

Næringsmedium
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)
Inkubasjonsatmosfære

37°C, 5% CO2, humidified atmosphere.

Kosttilskudd
Supplement the medium with 10% FBS
Dissosiasjonsmiddel
Accutase
Subkultivering
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.
Oppdelingsforhold
1 to 3
Såtetthet
2-4*10^4/cm²
Væskefornyelse
2 to 3 times per week
Tining og dyrking
  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

07Kvalitetskontroll og kryokonservering

Frysemedium
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Oppbevaringsbetingelser

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.

Fraktvilkår

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

Donorens alder
60 years
Etnisitet
European

10Produktdetaljer

Sammensetningstabell