Lenti-SV40T (Puro) Virus, High Titer
| Cat. No. | LV613 |
| Name | Lenti-SV40T (Puro) Virus, High Titer |
| Unit | 2 x 100 µl |
| Unpacking and Storage Instructions |
Lentiviruses are shipped with dry ice. For long term storage, it is recommended to store the viruses at -80°C in small aliquots to avoid repeated freeze-thaw cycles. |
| Description |
High-titer (109 IU/ml) recombinant lentivirus expressing the SV40 large T antigen (SV40T) for efficient immortalization of primary and finite-lifespan mammalian cells. SV40T extends cellular lifespan by functionally inactivating key cell cycle regulators, enabling the establishment of continuously proliferating cell lines while supporting stable long-term transgene expression. A puromycin resistance marker enables convenient antibiotic selection following transduction, while high viral titers maximize delivery efficiency across diverse cell types. |
| Application |
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| Shipping Conditions | Dry Ice |
| Expression System Type | Lentivirus |
| Caution |
This product is distributed for laboratory research only. |
| Material Citation | If use of this material results in a scientific publication, please cite the material in the following manner: Applied Biological Materials Inc, Cat. No. LV613 |
Print/Download Datasheet
| What primers can I use for SV40 large T detection? | |
|
•PCR primers:
SV40T Forward Primer Sequence
5’ AGCCTGTAGAACCAAACATT 3'
SV40T Reverse Primer Sequence
5’ CTGCTGACTCTCAACATTCT 3'
Expected band size: 792bp
•qPCR primers: SV40 Forward Primer Sequence
TTCCCTGACCTGAAGGCAAATC
SV40 Reverse Primer Sequence
GGCTGAACTTTGAGCTAGGAGTAG
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| Do I need to remove antibiotics (penicillin, streptomycin) before immortalizing my cells with the SV40T antigen viruses? | |
|
No. Routine cell culture antibiotics do not interfere with the SV40T antigen virus infection efficiency.
|
| What is the general procedure for immortalizing cells? | |
|
See our Cell Immortalization Handbook for more details.
|
| Can you recommend a specific reagent and protocol to immortalize my cell line? | |
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Successful cell immortalization is unpredictable and must be determined experimentally, as results vary with species, tissue origin, growth characteristics and whether or not specific cell functions need to be preserved.
Our in-house experiments using the SV40T and hTERT lentiviruses have achieved the highest immortalization success rates in a variety of different cell types. |
| Do immortalized cells retain all characteristics of the original primary cell line? | |
|
Not always. Some phenotypic or genetic changes may occur during immortalization. We recommend using our hTERT immortalization reagents as this method preserves phenotype and karyotype as well as minimizes genomic instability.
|
| Do I need a control when performing cell immortalization experiments? | |
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Yes. Always include control cells that are not transduced in order to compare growth rates and detect senescence bypass.
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| How do I confirm successful cell immortalization? | |
|
Assess long-term growth beyond normal passage limits and verify expression of the immortalizing genes via PCR, qPCR or Western blot.
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| Where can I learn more about cell immortalization? | |
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Check out our Learning Resources and Youtube video for more information.
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| How does the SV40T gene immortalize cells? | |
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SV40T works to shut down p53 and pRb-dependent growth control, thus over-riding the normal safety checkpoints that limit cell division.
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| Will this virus immortalize my primary cells? | |
|
This is highly dependent on the immortalization reagent and cell type. Check out our Cell Immortalization Reagents Compatibility Chart for more information.
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- Li An Wu, Feng, J., Wang, L., Yan Dong Mu, Baker, A., Donly, K. J., Jelica Gluhak-Heinrich, Harris, S. E., MacDougall, M., & Chen, S. (2010). Immortalized mouse floxed Bmp2 dental papilla mesenchymal cell lines preserve odontoblastic phenotype and respond to BMP2. Journal of Cellular Physiology, 225(1), 132–139. https://doi.org/10.1002/jcp.22204
- Olyslaegers, D. A. J., Lowiese M B Desmarets, Annelike Dedeurwaerder, Dewerchin, H. L., & Nauwynck, H. J. (2013). Generation and characterization of feline arterial and venous endothelial cell lines for the study of the vascular endothelium. BMC Veterinary Research, 9(1). https://doi.org/10.1186/1746-6148-9-170
- Lowiese MB Desmarets, Sebastiaan Theuns, Olyslaegers, D. A., Annelike Dedeurwaerder, Vermeulen, B. L., Roukaerts, I. D., & Nauwynck, H. J. (2013). Establishment of feline intestinal epithelial cell cultures for the propagation and study of feline enteric coronaviruses. Veterinary Research, 44(1). https://doi.org/10.1186/1297-9716-44-71
- Laval, K., Favoreel, H. W., Katrien C. K. Poelaert, Jolien Van Cleemput, & Nauwynck, H. (2015). Equine Herpesvirus Type 1 Enhances Viral Replication in CD172a + Monocytic Cells upon Adhesion to Endothelial Cells. 89(21), 10912–10923. https://doi.org/10.1128/jvi.01589-15
- Welzel, J., Grüdl, S., Banowski, B., Stark, H., Sättler, A., & Welss, T. (2022). A novel cell line from human eccrine sweat gland duct cells for investigating sweating physiology. International Journal of Cosmetic Science, 44(2), 216–231. Portico. https://doi.org/10.1111/ics.12769
- Lee, Y., Glorián Berríos-Vázquez, Maes, R. K., Matti Kiupel, Lowiese M.B. Desmarets, Nauwynck, H. J., & Gisela Soboll Hussey. (2023). Development of immortalized feline respiratory epithelial cells in an air-liquid-interface culture system for feline herpesvirus-1 study. Virus Research, 326, 199063–199063. https://doi.org/10.1016/j.virusres.2023.199063
- Bailey, K.L., Cartwright, S.B., Patel, N.S. et al. Porcine pancreatic ductal epithelial cells transformed with KRASG12D and SV40T are tumorigenic. Sci Rep 11, 13436 (2021). https://doi.org/10.1038/s41598-021-92852-2 Application: Cell Immortalization
- Tashiro, K., Segawa, T., Futami, T. et al. Establishment and characterization of a novel kidney cell line derived from the common bottlenose dolphin. In Vitro Cell.Dev.Biol.-Animal 59, 536–549 (2023). https://doi.org/10.1007/s11626-023-00786-y. Application: Cell Immortalization
- Shishi He, Xiaoyun Xiao and Rong Lei et al. Establishment of Breast Phyllodes Tumor Cell Lines Preserving the Features of Phyllodes Tumors. BIOI. 2023. Vol. 4(1):7-17. DOI: 10.15212/bioi-2022-0025. Application: Cell Immortalization.
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Alcock, D., Power, S., Hogg, B. et al. Generating bat primary and immortalised cell-lines from wing biopsies. Sci Rep 14, 27633 (2024). https://doi.org/10.1038/s41598-024-76790-3. Application: Cell Immortalization
- Liu X, Xia F, Wu X, Tang Y, Wang L, Sun Q, Xue M, Chang W, Liu L, Guo F, Yang Y and Qiu H (2021) Isolation of Primary Mouse Pulmonary Microvascular Endothelial Cells and Generation of an Immortalized Cell Line to Obtain Sufficient Extracellular Vesicles. Front. Immunol. 12:759176. doi: 10.3389/fimmu.2021.759176. Application: Cell Immortalization
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