Gene: TERT
Official Full Name: telomerase reverse transcriptaseprovided by HGNC
Gene Summary: Telomerase is a ribonucleoprotein polymerase that maintains telomere ends by addition of the telomere repeat TTAGGG. The enzyme consists of a protein component with reverse transcriptase activity, encoded by this gene, and an RNA component which serves as a template for the telomere repeat. Telomerase expression plays a role in cellular senescence, as it is normally repressed in postnatal somatic cells resulting in progressive shortening of telomeres. Deregulation of telomerase expression in somatic cells may be involved in oncogenesis. Studies in mouse suggest that telomerase also participates in chromosomal repair, since de novo synthesis of telomere repeats may occur at double-stranded breaks. Alternatively spliced variants encoding different isoforms of telomerase reverse transcriptase have been identified; the full-length sequence of some variants has not been determined. Alternative splicing at this locus is thought to be one mechanism of regulation of telomerase activity. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00197 | TERT Knockout cell line (HCT 116) | Human | TERT | 1:2~1:4 | Negative | Online Inquiry |
KO05401 | TERT Knockout cell line (HeLa) | Human | TERT | 1:3~1:6 | Negative | Online Inquiry |
KO05402 | TERT Knockout cell line (HEK293) | Human | TERT | 1:3~1:6 | Negative | Online Inquiry |
KO05403 | TERT Knockout cell line (A549) | Human | TERT | 1:3~1:4 | Negative | Online Inquiry |
TERT Gene Knockout Cell Lines are genetically modified cellular models that have had the telomerase reverse transcriptase (TERT) gene selectively disrupted. The TERT gene is critical for the maintenance of telomere length, thereby playing a pivotal role in cellular aging and stability. By knocking out TERT, these cell lines facilitate the study of telomere dynamics, cellular senescence, and the underlying mechanisms of cancer biology linked to telomerase activity.
The primary function of TERT Gene Knockout Cell Lines is to provide researchers with a reliable system to explore the consequences of telomere shortening and the resulting senescence or apoptosis in somatic cells. The knockout mechanism is typically achieved through CRISPR-Cas9 technology, allowing precise edits that abolish TERT expression, leading to the accelerated aging of the cells. Researchers can use these models to investigate the biological processes related to telomere shortening, such as chromosomal instability and gene expression changes, lending insights into various diseases, particularly age-related disorders and cancers.
The scientific importance of TERT Gene Knockout Cell Lines extends to their applications in fundamental research as well as in translational studies. They serve as valuable tools in cancer research to investigate the role of telomerase in malignancy and to test novel therapeutic strategies aimed at exploiting telomere biology. Furthermore, these cell lines are increasingly utilized in drug development and regenerative medicine for evaluating the effects of potential therapeutics on cellular aging.
What sets our TERT Gene Knockout Cell Lines apart from alternatives on the market is their rigorously validated design, ensuring consistent performance and reproducibility in experiments. Our product is derived from well-characterized human cell lines, ensuring broader applicability in diverse research scenarios.
Researchers, clinicians, and institutions looking to deepen their understanding of telomere biology will find these cell lines invaluable, as they pave the way for innovative exploration and potential breakthroughs in therapies targeting age-related conditions and cancer.
As a company committed to advancing biological research, we leverage years of expertise in genetic engineering to provide high-quality products that support cutting-edge studies, ensuring our clients can push the boundaries of scientific discovery effectively.
Please note that all services are for research use only. Not intended for any clinical use.
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