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CMV-hTERT(GFP, Puro) Lentiviral Particles

For research use only. Not intended for any clinical use.

Cat. No. :   LVIM035Z

Storage :   -80℃ Shipping :   Frozen on dry ice

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Virus Particles Information

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Gene Information

Cat. No. LVIM035Z
Description This lentivirus expresses human TERT under the control of CMV promoter. It also contains GFP reporter gene and puromycin resistance gene for selection. This virus can be used for cell immortalization.
Gene TERT
Titer Varies lot by lot, for example, ≥1*10^7 TU\/mL, ≥1*10^8 TU\/mL, ≥1*10^9 TU\/mL etc.
Size Varies lot by lot, for example, 100 ul, 500 ul, 1 mL etc.
Storage Store at -80℃. Avoid multiple freeze\/thaw cycles.
Shipping Frozen on dry ice
Summary Creative Biogene ensures high-quality lentivirus particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between lentivirus particle lots.
Mycoplasma Creative Biogene routinely tests for mycoplasma contamination using a mycoplasma detection kit. Cell lines are maintained for approximately 20 passages before being discarded and replaced with a new vial of early passage cells. Approximately 2 weeks after thawing, cell culture supernatants are tested for mycoplasma contamination. Creative Biogene ensures that lentiviral products are free of mycoplasma contamination.
Purity Creative Biogene evaluates the level of impurities, such as residual host cell DNA or proteins, in prepared lentiviral vectors to ensure they meet quality standards.
Sterility The lentiviral samples were inoculated into cell culture medium for about 5 days and the growth of bacteria and fungi was tested. Creative Biogene ensures that the lentiviral products are free of microbial contamination.
Transducibility Upon requirement, Creative Biogene can perform in vitro or in vivo transduction assays to evaluate the ability of lentivirus to deliver genetic material into target cells, and assess gene expression and functional activities.
Proviral Identity Confirmation All Creative Biogene lentiviral vectors are confirmed to have correctly integrated provirus using PCR. This test involves transducing cells with serial dilutions of the lentiviral vector, harvesting the cells a few days later, and isolating genomic DNA. This DNA is then used as a template to amplify a portion of the expected lentiviral insert.
Target Gene TERT
Background 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]
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CMV-hTERT(GFP, Puro) lentiviral particles are sophisticated tools for gene manipulation and cell engineering, designed to deliver the human telomerase reverse transcriptase (hTERT) gene into target cells. This lentiviral vector system utilizes the EF1α promoter to drive hTERT expression, renowned for its potent and constitutive expression in mammalian cells. The introduction of GFP (green fluorescent protein) serves as a visual reporter gene, enabling researchers to easily monitor transduction efficiency and track transduced cells using fluorescence microscopy or flow cytometry. Furthermore, a puromycin resistance gene provides an efficient screening mechanism, enriching successfully transduced cells upon puromycin treatment. This dual screening feature ensures high purity and homogeneity of the cell population, crucial for subsequent experiments. The lentiviral backbone itself offers numerous advantages, such as high transduction efficiency, stable integration into the host genome, and the ability to infect both dividing and non-dividing cells, making it suitable for a variety of cell types.

The primary application of this lentiviral vector is cell immortalization, a key process for extending the lifespan of primary cells cultured in vitro. By introducing hTERT (a gene that maintains telomere length and inhibits cellular senescence), researchers can establish stable cell lines that retain key physiological characteristics of primary cells. This is particularly important for studying long-term cellular processes, disease modeling, and drug screening, as the limited lifespan of cells often restricts experimental scope. The system also supports functional genomics research, such as CRISPR screening libraries, where hTERT expression ensures cell survival in long-term experiments. Overall, this lentiviral tool accelerates research in aging, cancer biology, regenerative medicine, and tissue engineering by providing a reliable method for generating immortalized cells with traceable markers and selectable characteristics.

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Customer Reviews
User-Friendly Protocol

The provided guidelines were clear, and the virus integrated efficiently. Observed extended cell lifespan within weeks. Very satisfied!

Canada

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