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SV40T Antigen Overexpression Viruses for Cell Immortalization

 

SV40T antigen overexpression viruses are recombinant lentiviral particles that deliver the simian virus 40 (SV40) large T antigen gene, which inactivates the p53 and Rb tumor suppressor pathways to bypass senescence checkpoints and immortalize primary cells across human, mouse, rat, and other mammalian species. They are supplied under CMV or EF1-alpha promoters with antibiotic or fluorescent-antibiotic fusion selection markers. Academic researchers immortalizing cells from non-human or difficult-to-immortalize primary tissue can use MBP's specialist team to confirm vector format before ordering.

Explore available SV40T antigen viral reagents or request a quotation by contacting customerservice@mbpinc.net. Our team can help confirm vector design, promoter selection, and suitability for your specific immortalization system.

SV40T Antigen Overexpression Viruses

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Adeno-SV40 Adenovirus
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Lenti-SV40 (tsA58 temperature sensitive mutant) (No Selection Marker) Lentivirus, High Titer
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Lenti-SV40 (tsA58 temperature sensitive mutant) Lentivirus, High Titer
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Lenti-SV40 Lentivirus, High Titer
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Lenti-SV40T  (No Selection Marker) Lentivirus, High Titer
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Lenti-SV40T (Neo) Lentivirus, High Titer
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Lenti-SV40T (Puro) Lentivirus, High Titer
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Lenti-SV40Tt Lentivirus, High Titer
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Retro-SV40 Retrovirus
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Retro-SV40LT Retrovirus
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What are SV40T antigen overexpression viruses?

 

SV40T antigen overexpression viruses are recombinant lentiviral particles carrying the simian virus 40 (SV40) large T antigen gene, a hexamer protein that inactivates the p53 and retinoblastoma (Rb) tumor suppressor pathways, bypassing the senescence checkpoints that normally limit primary cell proliferation. Some constructs deliver the large T antigen alone, while others include both large and small T antigens. Related entities include p53/Rb pathway inactivation, broad cross-species immortalization (human, mouse, rat, bovine, porcine, canine), karyotype/tumorigenicity characterization (soft agar assay), and antibiotic/fluorescent selection markers.

 

What you will find:

 

  • Lenti-SV40 (tsA58 Mutant) for cell proliferation with inducible control and temperature-sensitive expression
  • Lenti-SV40T (Puro/Neo/No Marker) provides stable integration with versatile selection markers of highly concentrated lentiviral stocks 
  • Adeno-SV40 Adenovirus for transient T-antigen expression with high-efficiency adenoviral vectors
  • Retro-SV40 & Retro-SV40LT for special integration in proliferating cells.
  • Lenti-SV40Tt Lentivirus: Small T and Large T antigens for improved transformation.

 

How to choose SV40T antigen overexpression virus products

 

Large T antigen alone vs. large and small T antigen

Constructs delivering large T antigen alone target p53/Rb pathway inactivation specifically, while large-and-small-T constructs include additional SV40 small T antigen activity affecting protein phosphatase 2A (PP2A) signaling; confirm which form a published protocol specifies, since the two can produce different immortalization efficiencies and phenotypes.

Species applicability

SV40 large T antigen has documented immortalization success across human, mouse, rat, bovine, porcine, and canine primary cells, making it a broadly applicable option when hTERT (human-specific) is not suitable for the target species.

Selection marker and promoter

As with TERT lentivirus, SV40T constructs are available under CMV or EF1-alpha promoters with antibiotic resistance (puromycin, hygromycin, blasticidin, neomycin/G418, zeocin) or fluorescent-antibiotic fusion markers (GFP-Bsd, RFP-Puro); select based on the target cell line's existing markers and expected culture duration.

Post-immortalization characterization

Because SV40 large T antigen inactivates tumor suppressor pathways, immortalized lines should be characterized for karyotype changes and tested by assays such as soft agar colony formation and tumorigenicity testing if downstream applications require confirmation that the line has not undergone malignant transformation.

 

Specifications context

 

SV40T antigen lentivirus is typically supplied at titers around 1x10^8 TU/mL, shipped on dry ice and stored at -80°C, with constructs validated by full-length sequencing and confirmed free of common contaminants. Immortalized lines derived from SV40T transduction are commonly characterized by Western blot or immunofluorescence confirming SV40-LT protein expression, alongside marker expression comparison to the original primary cells. As of 2026, SV40 large T antigen remains the most broadly cross-species-applicable immortalization approach, often selected when hTERT (human-specific) is not an option for the target species or when faster immortalization is prioritized over preserving the original phenotype.

This sub-category sits within MBP's cell immortalization catalog alongside TERT overexpression viruses and additional immortalization agents. Labs constructing custom SV40T expression vectors can also review MBP's cloning reagents. MBP's specialist team can help confirm species applicability and vector format for a specific primary cell type before order placement.

Contact the expert team at MBP today to get high-quality SV40T antigen overexpression viruses.

FAQ

SV40 large T antigen is a hexamer protein that inactivates the p53 and retinoblastoma (Rb) tumor suppressor pathways, bypassing the senescence checkpoints that normally limit primary cell proliferation. This mechanism differs from hTERT, which extends telomeres rather than inactivating tumor suppressor pathways directly.
Constructs delivering SV40 large T antigen alone target p53/Rb pathway inactivation specifically, while large-and-small-T antigen constructs include additional SV40 small T antigen activity affecting protein phosphatase 2A (PP2A) signaling. The two forms can produce different immortalization efficiencies and resulting cell phenotypes, so the published protocol's specified form should be used.
SV40 large T antigen has documented immortalization success across human, mouse, rat, bovine, porcine, and canine primary cells, making it a broadly applicable option for species where hTERT, which is human-specific, is not suitable. This cross-species applicability is one of the main reasons SV40T is chosen over TERT for non-human primary cell immortalization.
SV40 large T antigen immortalization inactivates tumor suppressor pathways, so immortalized lines should be characterized for karyotype changes and tested by assays such as soft agar colony formation if downstream applications require confirmation the line has not undergone malignant transformation. Some published studies report SV40T-immortalized cells that retain proliferation without malignant transformation by these assays, but characterization should be done for each new line.
SV40T antigen lentivirus constructs are available under CMV or EF1-alpha promoters, similar to hTERT lentivirus options. EF1-alpha is often selected for extended culture where CMV promoter silencing is a concern, while CMV provides strong initial expression suitable for shorter-term experiments.
SV40 large T antigen and hTERT can be combined for primary cell types that resist immortalization by either factor alone, since the two act through different mechanisms (tumor suppressor pathway inactivation versus telomere extension). This combination approach is more commonly needed for certain epithelial or stromal cell types.
SV40T antigen lentivirus is commonly available with antibiotic resistance markers including puromycin, hygromycin, blasticidin, neomycin/G418, and zeocin, as well as fluorescent-antibiotic fusion markers such as GFP-Bsd or RFP-Puro. Confirm the selection marker does not conflict with any existing genetic modifications in the target cell line.
SV40 large T antigen (SV40-LT) expression is commonly confirmed by Western blot or immunofluorescence staining for the SV40-LT protein in transduced cells, alongside PCR detection of the integrated transgene. Marker expression comparison to the original primary cells is often performed alongside SV40-LT confirmation to characterize the resulting immortalized line.
SV40T-immortalized cell lines generated with research-grade lentivirus are labeled research use only (RUO), and the inactivation of p53/Rb pathways combined with integrated viral genetic material generally makes them unsuitable for direct therapeutic use without substantial additional regulatory-grade development. Labs pursuing clinical-adjacent applications should consider hTERT-based approaches, which may better preserve normal cell regulation, as an alternative starting point.
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