SF188 Cells
| Unit |
3 x 10^6 cells/ml |
|---|---|
| Cell Type |
Tumor Cells |
| Tissue Type |
Brain cancer cell lines |
| 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 and 1% NEAA. Dissociation reagent: Accutase. Seeding density: 2 to 4 x 10⁴ cells/cm². 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. Incubation atmosphere: 37°C ,5% CO2 ,humidified atmosphere. |
| Immortalization Method | |
| Full Information |
The SF188 cell line is a human glioblastoma multiforme (GBM) model established from a pediatric patient. It is used extensively to study the mechanisms of chemotherapeutic resistance, particularly to alkylating agents such as 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU). Compared to other glioma-derived cell lines such as SF126, SF188 exhibits significantly higher resistance to BCNU-induced cytotoxicity and genotoxicity. Specifically, SF188 shows approximately threefold greater resistance in survival assays and 14-fold lower susceptibility to BCNU-induced sister chromatid exchange (SCE), indicating a robust DNA damage tolerance phenotype.
The resistance in SF188 is attributed to enhanced DNA repair capacity, especially the rapid and efficient removal of O6-alkylguanine adducts. Upon exposure to methylating agents like N-methyl-N-nitrosourea, SF188 cells demonstrate marked removal of O6-methylguanine lesions, whereas more sensitive cell lines show minimal repair activity. This efficient lesion repair likely prevents the formation of interstrand crosslinks, thereby maintaining genomic integrity and increasing cell survival. Importantly, SF188 also exhibits a high chromosomal count (modal number 91) and lacks expression of glial fibrillary acidic protein (GFAP), confirming its poorly differentiated glioma origin and making it an excellent model for studying the interplay between DNA repair and chemoresistance in high-grade gliomas.
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

