H4-II-E-C3 Cells

Unit

3 x 10^6 cells/ml

Cell Type

Tumor Cells

Tissue Type

Rat cell lines

Organism

Rat

Donor History

Hepatocellular carcinoma

Growth Properties

Adherent

Growth Conditions

Culture medium: 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). Supplements: Supplement the medium with 10% FBS. Dissociation reagent: Accutase. Seeding density: 1-3*10^4/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

https://www.cytion.com/H4-II-E-C3-Cells/305336

SKU: 305336 Kategorie: ,
Mgr. Otakar Fišer
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Mgr. Otakar Fišer
Produktový manažer - Life Science
Popis

The H4-II-E-C3 cell line is a well-established rat hepatoma cell line derived from liver carcinoma. This line is widely used in research focused on liver-specific functions and the metabolic processes that occur within hepatocytes. One notable aspect of H4-II-E-C3 cells is their high expression of the high-affinity glutamate transporter GLT-1A. This feature distinguishes them from normal rat hepatocytes, which do not exhibit significant levels of this transporter. The expression of GLT-1A in H4-II-E-C3 cells allows for the efficient study of glutamate metabolism and transport, providing insights into liver cell transformation and tumor cell metabolism.

Additionally, H4-II-E-C3 cells are used to study aldehyde metabolism, particularly the activity of mitochondrial class 2 aldehyde dehydrogenase (ALDH2). This enzyme is critical for metabolizing acetaldehyde produced during ethanol oxidation, making this cell line suitable for research on alcohol metabolism and its cellular effects. The use of an “acetaldehyde clamp” technique in these cells has allowed precise measurement of ALDH2 activity without the need for mitochondrial isolation, facilitating the study of enzyme kinetics and the impact of various inhibitors on aldehyde detoxification.

O značce

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.