概要:The adaptation of the HEK293 cell line to suspension culture resulted in robust growth and achieved similar or improved maximum cell density compared to adherent cultures.
This transition to suspension culture simplifies subcultivation, enhances scalability, and reduces production costs, making it an advantageous approach for large-scale manufacturing of biotechnological products.
The HEK293 cell line, initially derived in the 1970s, arose from the transformation of human embryonic kidney cells with sheared adenovirus 5 DNA, leading to approximately 30% of cells exhibiting hypotriploid karyotypes with 64 modal chromosomes and 4.2% with higher ploidies.
The multiple copies of adenovirus E1A and E1B genes in HEK293 cells result in high transfection efficiency, making them valuable in biotechnology for protein expression, gene therapy, and vaccine production.
Moreover, the pharmaceutical industry employs HEK293 cells for high-throughput screening assays due to their ability to be transfected with plasmids encoding drug targets and cultured in large numbers.
In industrial biotechnology, HEK293 cells serve as hosts for producing recombinant proteins, enzymes, and biosensors.
Additionally, HEK293 cells are essential in toxicology research for studying the effects of chemicals and environmental toxins on cellular processes and gene expression.
Notably, the HEK293 cell line is also utilized to generate recombinant viruses like adenovirus and lentivirus for gene therapy, viral replication, and host-virus interactions.
Overall, the suspension-adapted HEK293 cell line, along with its versatile applications in biomedical research, biotechnology, pharmaceuticals, and toxicology, signifies a significant advancement in the field of cell culture technology.
仕様
容量:1vial
カテゴリー:Kidney cancer cell lines | Transformed cell lines
Organism:Human
Tissue:Kidney
Applications:Transfection host
Age:Fetus
Gender:Female
Growth Properties:Suspension
Citation:HEK293 suspension-adapted (Cytion catalog number 300686)
Biosafety Level:1
Receptors Expressed:Vitronectin
Protein Expression:CEA negative, p53 positive
Tumorigenic:In nude mice
Virus Susceptibility:transformed with adenovirus 5 DNA adenovirus 5 DNA