Siirry sisältöön
LN229-Luc
Kudos
Brain, right frontal parieto-occipital cortex
Sairaus
Glioblastoma
Synonyymit
LN 229, LN229, LNT-229

Asiakirjat

LN229-Luc

Cell line · Tuotenumero 305692

LN229-Luc on ihmisen LN229-glioblastoomasolulinjan bioluminesoiva johdannainen, joka on muokattu ilmentämään vakaasti tulikärpäsen lusiferaasi-raportointigeeniä. P...

€550.00ilman veroja ja toimituskuluja

Räätälöinti / Suositukset

Varastossa
Lot
Suositeltava (tuorein erä)
  • CoA
1

01Yleistä tietoa

Kuvaus

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.

Kudos
Brain, right frontal parieto-occipital cortex
Sairaus
Glioblastoma
Synonyymit
  • LN 229
  • LN229
  • LNT-229

02Luokittelu

Organismi
Ihminen
Sukupuoli
Nainen
Kasvuominaisuudet
Kiinnittynyt
GMO-status
GMO-S1
GMO-statuksen tiedot
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.
Bioturvallisuustaso
1

03Ominaisuudet

Morfologia
Epithelial

04Tunnisteet

Lähdeviite
LN229-Luc (Cytion catalog number 305692)
NCBI-verotunnus
9606
Cellosaurus
CVCL_0393

05Ilmentyminen ja alttius

Proteiinin ilmentyminen
Luc
Antigeenin ilmentyminen
Luc2 (firefly, codon-optimized)

06Käsittely ja viljely

Viljelyalusta
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)
Inkubaatioilma

37°C, 5% CO2, humidified atmosphere.

Ravintolisät
Supplement the medium with 10% FBS
Dissosiaatioreagenssi
Accutase
Soluviljely
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.
Jakosuhde
1 to 3
Kylvötiheys
2-4*10^4/cm²
Nesteen uusiminen
2 to 3 times per week
Sulatus ja viljely
  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

07Laadunvalvonta ja kryosäilytys

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

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.

Toimitusehdot

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.

08Lahjoittaja

Luovuttajan ikä
60 years
Etnisyys
European

10Tuotetiedot

Koostumustaulukko