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TERT Overexpression Viruses for Cellular Immortalization and Senescence Bypass

 

TERT overexpression viruses are recombinant lentiviral particles that deliver human telomerase reverse transcriptase (hTERT) under a constitutive promoter to extend telomeres and bypass replicative senescence in primary cells. They are supplied with antibiotic or fluorescent-antibiotic fusion selection markers under CMV or EF1-alpha promoters. Academic researchers immortalizing fibroblasts or other primary cell types while preserving near-normal phenotype can use MBP's specialist team to confirm titer and marker selection before ordering.

Explore available TERT overexpression viral reagents or request a quotation by contacting customerservice@mbpinc.net. Our team can help confirm viral titer, promoter design, and selection marker compatibility for your immortalization workflow.

TERT Overexpression Viruses

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Adeno-hTERT
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USD1,423.52
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USD1,016.80
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Adeno-hTERT Antisense
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USD1,284.64
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USD917.60
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Lenti-EF1a-hTERT Virus, High Titer
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USD1,423.52
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USD1,016.80
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Lenti-EF1a-hTERT-Hygro Virus, High Titer
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USD1,423.52
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USD1,016.80
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Lenti-hTERT (No Selection Marker) virus, High Titer
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USD1,423.52
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USD1,016.80
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Lenti-hTERT Virus, High Titer
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USD1,423.52
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USD1,016.80
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Lenti-hTERT-2A-CDK4 Virus, High Titer
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USD1,423.52
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USD1,016.80
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Lenti-hTERT-Neo Virus, High Titer
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USD1,423.52
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USD1,016.80
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What are TERT overexpression viruses?

 

TERT overexpression viruses are recombinant lentiviral (or in some cases retroviral) particles carrying the human telomerase reverse transcriptase (hTERT) gene under a constitutive promoter, designed to extend telomere length and bypass replicative senescence in primary cells. Related entities include telomere maintenance, replicative senescence, population doubling limits, EF1-alpha and CMV promoters, and antibiotic/fluorescent selection markers (puromycin, hygromycin, GFP-Puro).

 

What you will find:

 

  • Adeno-hTERT Antisense used in cancer research for inhibition of telomerase activity 
  • Lenti-hTERT Virus (High Titer) used as a standard tool for efficient immortalization of primary cells 
  • Lenti-EF1a-hTERT Virus uses the EF1a promoter for reliable, long-term expression.
  • Adeno-hTERT is used in transient TERT expression for high-efficiency adenoviral delivery
  • Lenti-hTERT is used as a streamlined vector for specialized genetic engineering.
  • Lenti-hTERT-2A-CDK4 Virus co-expression for complex cell types like myogenic cells.
  • Lenti-EF1a-hTERT-Hygro Virus for precise metabolic selection featuring hygromycin resistance 
  • Lenti-hTERT-Neo Virus for stable generation of cell lines, includes neomycin/G418 resistance 

 

How to choose TERT overexpression virus products

 

Promoter selection

EF1-alpha promoter constructs are often preferred for primary cells where CMV promoter silencing over extended culture is a concern, though CMV-driven constructs offer strong initial expression; the choice may depend on the expected culture duration and cell type-specific promoter activity.

Selection marker type

Antibiotic resistance markers (puromycin, hygromycin, neomycin/G418, blasticidin) allow selection of stably transduced populations by drug treatment, while fluorescent-antibiotic fusion markers (e.g., GFP-Puro) additionally allow visual confirmation of expression and flow sorting; confirm the target cell line's existing markers don't conflict.

Titer and transduction efficiency

hTERT lentivirus is typically supplied at titers around 1x10^8 TU/mL; transduction efficiency depends on the target cell type's susceptibility to lentiviral infection, and some difficult-to-transduce primary cells may require optimization of multiplicity of infection (MOI) or use of transduction enhancers.

Species considerations

hTERT is human-specific; for non-human primary cells, confirm whether a species-matched TERT ortholog is available or whether SV40 large T antigen (with broader documented cross-species activity) is a more appropriate alternative for the target species.

 

Specifications context

 

TERT overexpression lentivirus is typically supplied at approximately 1x10^8 TU/mL in small-volume vials (e.g., 25 microliters per vial), shipped on dry ice and stored at -80°C, with constructs validated by full-length sequencing and confirmed free of mycoplasma and common contaminants. Stable transduction and selection typically take 1-2 weeks before characterization, with full confirmation of telomere extension and extended proliferative capacity assessed over subsequent passages. As of 2026, hTERT lentivirus remains a standard tool for generating immortalized cell lines that retain much of the original primary cell's phenotype, distinguishing it from the more transformation-prone SV40 large T antigen approach.

This sub-category sits within MBP's cell immortalization catalog alongside SV40T antigen overexpression viruses and additional immortalization agents. Labs building custom expression constructs can also review MBP's cloning reagents for vector and competent cell options. MBP's specialist team can help confirm promoter and selection marker choices for a specific primary cell type before order placement.

Browse our collection and contact the expert team at MBP today to find premium-quality TERT viral vectors for your lab. 

FAQ

hTERT lentivirus delivers the human telomerase reverse transcriptase gene under a constitutive promoter, which extends telomere length in transduced cells and allows them to bypass the replicative senescence that normally limits primary cell division. This approach often preserves a near-normal karyotype and phenotype compared to oncogene-based immortalization methods.
hTERT lentivirus is typically supplied at titers around 1x10^8 transducing units per mL (TU/mL), shipped on dry ice for storage at -80°C upon receipt. The actual transduction efficiency achieved depends on the target cell type's susceptibility to lentiviral infection and the multiplicity of infection used.
EF1-alpha promoter constructs are often preferred for primary cells intended for long-term culture, since CMV promoter activity can be silenced over extended passaging in some cell types. CMV-driven constructs provide strong initial expression and may be suitable for shorter-term experiments or cell types less prone to CMV silencing.
Human TERT (hTERT) lentivirus is primarily validated for human primary cells, and is species-specific for its intended target. For non-human primary cells, a species-matched TERT ortholog or an alternative approach such as SV40 large T antigen, which has broader documented cross-species activity, may be more appropriate.
Antibiotic selection of stably transduced cells after hTERT lentivirus transduction typically takes 1-2 weeks, depending on the antibiotic concentration and the cell type's sensitivity. Confirmation of stable integration and hTERT expression by PCR or other methods follows the initial selection period.
hTERT immortalization can be combined with SV40 large T antigen for primary cell types that resist immortalization by hTERT alone, since the two factors act through different mechanisms. Combination approaches are more commonly needed for certain epithelial or stromal cell types compared to fibroblasts, which often immortalize successfully with hTERT alone.
hTERT lentivirus is commonly available with antibiotic resistance markers such as puromycin, hygromycin, blasticidin, and neomycin/G418, as well as fluorescent-antibiotic fusion markers like GFP-Puro for combined drug selection and visual confirmation. Confirm the selection marker does not conflict with any existing genetic modifications in the target cell line.
Successful hTERT immortalization is typically confirmed by PCR analysis of transgene expression, comparison of morphology and marker expression to the original primary cells, and demonstration of extended proliferative capacity beyond the normal replicative senescence point. Telomere length measurement can also be used to directly confirm the telomerase-mediated mechanism.
hTERT-immortalized cell lines generated with research-grade lentivirus are labeled research use only (RUO) and carry integrated viral genetic material, which generally makes them unsuitable for direct therapeutic use without additional regulatory-grade development. Labs pursuing clinical-adjacent applications should plan for additional characterization beyond standard research immortalization.
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