HK Mad2-LAP/H2B-mCherry Cells

Unit

3 x 10^6 cells/ml

Cell Type

Stable (KO/Expressing) Cells

Tissue Type

Reporter-labeled cells

Organism

Human

Donor History

Carcinoma

Growth Properties

Monolayer

,

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 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

https://www.cytion.com/HK-Mad2-LAP-H2B-mCherry-Cells/300920

Mgr. Otakar Fišer
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Mgr. Otakar Fišer
Produktový manažer - Life Science
Popis

The HK Mad2-LAP/H2B-mCherry cell line is a genetically engineered cell model extensively utilized for studying chromosome segregation and the spindle assembly checkpoint during mitosis. These cells are derived from HeLa Kyoto cells, a robust human cell line originally taken from a cervical carcinoma. The HK Mad2-LAP (LAP-tagged Mad2) aspect of the cell line facilitates the visualization and functional analysis of the Mad2 protein, a critical component of the spindle assembly checkpoint that prevents anaphase onset until all chromosomes are properly aligned at the metaphase plate.
Incorporation of H2B-mCherry, where histone H2B is tagged with the mCherry fluorescent protein, allows for real-time imaging of chromatin dynamics during cell division. This feature makes the HK Mad2-LAP/H2B-mCherry cell line an excellent tool for high-resolution live-cell imaging techniques to observe chromosomal movements and mitotic progression in human cells under various experimental conditions. The use of fluorescent tags aids in precise tracking and quantification, thereby providing valuable insights into the molecular mechanisms governing cell cycle regulation and chromosomal stability.

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.