U-87 MG-RFP Cells
| Unit |
3 x 10^6 cells/ml |
|---|---|
| Cell Type |
Stable (KO/Expressing) Cells |
| Tissue Type |
Brain cancer cell lines ,Reporter-labeled cells |
| Organism |
Human |
| Donor History |
Glioblastoma |
| Growth Properties |
Adherent |
| Growth Conditions |
Culture medium: EMEM (MEM Eagle) ,w: 2 mM L-Glutamine ,w: 2.2 g/L NaHCO3 ,w: EBSS (Cytion article number 820100a). Supplements: Supplement the medium with 10% FBS. Dissociation reagent: Accutase. Seeding density: 1.5 to 2 x 10⁴ cells/cm². Freeze medium: As a cryopreservation medium ,we use complete growth medium + 10% DMSO for adequate post-thaw viability. Incubation atmosphere: 37°C ,5% CO2 ,humidified atmosphere. |
| Immortalization Method | |
| Full Information |
U-87 MG-RFP cells are a fluorescently labeled variant of the human glioblastoma astrocytoma cell line U-87 MG, which was originally derived from a malignant glioma tumor of an adult patient. The parental U-87 MG line is widely used as an in vitro model for glioblastoma due to its well-characterized growth properties, tumorigenic potential, and relevance to high-grade astrocytic tumors. These cells exhibit adherent growth with epithelial-like morphology and are commonly employed to study processes such as cell proliferation, invasion, angiogenesis, and response to hypoxic conditions.
In U-87 MG-RFP cells, stable expression of red fluorescent protein (RFP) enables real-time visualization of tumor cell behavior in both in vitro and in vivo systems. This modification facilitates applications such as live-cell imaging, tumor tracking in orthotopic xenograft models, and analysis of invasive growth patterns within brain tissue. U-87 MG-RFP cells are particularly valuable for studying glioblastoma progression, tumor–microenvironment interactions, and evaluating therapeutic strategies using fluorescence-based imaging approaches.
Genetic modification: Stably modified by replication-incompetent lentiviral transduction to express a red fluorescent protein (RFP) reporter; maintained as a polyclonal population under puromycin selection (1–5 µg/mL). S1/BSL-1 containment.
Společnost Cytion vznikla v roce 2004 v německém Heidelbergu s jasným vědeckým posláním: dodávat ověřené lidské a zvířecí buněčné linie bez kontaminace, připravené za přísně kontrolovaných laboratorních podmínek.
Postupně se vypracovala ve spolehlivou buněčnou banku, která slouží akademickým laboratořím, biotechnologickým firmám i farmaceutickým výzkumným týmům po celém světě. Klade přitom důraz na reprodukovatelnost výsledků, přísnou kontrolu kvality a dlouhodobá partnerství.
Mikrobiologické aplikace
NGS
Rapid testy
PCR plasty
Třepačky
Suché lázně
Fluorometry
Buněčné kultury
PCR, qPCR, RT
Detekce Mycoplasmat
Reverzní transkripce
Alergie
Intolerance
Elisa
Imunologické analyzátory
Veterinární imunologie
Alergie u zvířat
Intolerance u zvířat
Čtečky identifikačních čipů
Termočipy
Biochemie
Imunoanalýza

