DSL-6B-C2 Cells
| Unit |
3 x 10^6 cells/ml |
|---|---|
| Cell Type |
Tumor Cells |
| Tissue Type |
Rat cell lines |
| Organism |
Rat |
| Donor History |
Carcinoma |
| Growth Properties |
Adherent |
| Growth Conditions |
Culture medium: DMEM:Ham's F12 (1:1) ,w: 3.1 g/L Glucose ,w: 2.5 mM L-Glutamine ,w: 15 mM HEPES ,w: 0.5 mM Sodium pyruvate ,w: 1.2 g/L NaHCO3 (Cytion article number 820400a). Supplements: Supplement the medium with 10% FBS. Dissociation reagent: Accutase. Seeding density: 1 x 10⁴ cells/cm² will yield in a confluent layer in about 4 days. 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 DSL-6B/C2 cell line is derived from the DSL-6 transplantable acinar cell carcinoma of the pancreas, specifically established from a tumor model in a male Lewis rat. This model was initiated in 1986 from a primary acinar cell carcinoma that developed after intraperitoneal administration of azaserine, a potent carcinogen. The significance of this cell line stems from its origin in pancreatic cancer research, highlighting its utility in studying the biology and underlying mechanisms of pancreatic acinar cell carcinomas.
Initially, upon establishment in culture, DSL-6B/C2 cells exhibited the characteristic production of amylase, a hallmark of pancreatic exocrine function. However, this exocrine enzyme production was transient, ceasing within one to two weeks of culture. This change in phenotypic expression is notable as it suggests an adaptation to the in vitro environment, which may affect the cells’ utility in certain types of biological assays. The loss of amylase production might also reflect changes in cell differentiation or the emergence of subpopulations within the cultured cells, which could be critical for researchers focusing on the evolution of tumor cell characteristics in vitro.
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

