Lenti-hTERT (Puro) Virus, High Titer

Cat. No.
LV615
Unit
2 x 100 µl
Price
$1,025.00
Cat. No. LV615
Name Lenti-hTERT (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 hTERT gene.  

Application

Cell immortalization.

Storage Condition For long term storage, it is recommended to store the viruses at -80°C in small aliquots to avoid repeated freeze-thaw cycles.
Shipping Conditions Shipped with dry ice
Expression System Type Lentivirus
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. LV615
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Supporting Protocol
  • 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
  • Jung, A. R., Yoo, J. E., Shim, Y.-H., Choi, Y.-N., Jeung, H.-C., Chung, H. C., Rha, S. Y., & Oh, B.-K. (2013). Increased alternative lengthening of telomere phenotypes of telomerase-negative immortal cells upon trichostatin -a treatment. PubMed, 33(3), 821–829.
  • Zhou, G. L., Soon-Young Na, Rasma Niedra, & Seed, B. (2014). Deficits in receptor-mediated endocytosis and recycling in cells from mice bearing a disruption of the Gpr107 locus. Journal of Cell Science. https://doi.org/10.1242/jcs.135269
  • Krishna, V. D., Roach, E., Zaidman, N. A., Panoskaltsis-Mortari, A., Rotschafer, J. H., O’Grady, S. M., & Maxim C-J. Cheeran. (2015). Differential Induction of Type I and Type III Interferons by Swine and Human Origin H1N1 Influenza A Viruses in Porcine Airway Epithelial Cells. PLoS ONE, 10(9), e0138704–e0138704. https://doi.org/10.1371/journal.pone.0138704
  • Huang, H.-S., Chu, S.-C., & Chu, T.-Y. (2015). Efficient analyses of DNA double-strand breaks and the cell cycle in the secretory epithelial cells of fallopian tube fimbriae. Tzu Chi Medical Journal, 27(3), 102–106. https://doi.org/10.1016/j.tcmj.2015.05.004
  • Cacchiarelli, D., Trapnell, C., Ziller, M. J., Soumillon, M., Cesana, M., Karnik, R., Donaghey, J., Smith, Z. D., Ratanasirintrawoot, S., Zhang, X., Ho Sui, S. J., Wu, Z., Akopian, V., Gifford, C. A., Doench, J., Rinn, J. L., Daley, G. Q., Meissner, A., Lander, E. S., & Mikkelsen, T. S. (2015). Integrative Analyses of Human Reprogramming Reveal Dynamic Nature of Induced Pluripotency. Cell, 162(2), 412–424. https://doi.org/10.1016/j.cell.2015.06.016
  • Huang, H.-S., Chu, S.-C., Hsu, C.-F., Chen, P.-C., Ding, D.-C., Chang, M.-Y., & Chu, T.-Y. (2015). Mutagenic, surviving and tumorigenic effects of follicular fluid in the context of p53 loss: initiation of fimbria carcinogenesis. Carcinogenesis, 36(11), 1419–1428. https://doi.org/10.1093/carcin/bgv132
  • 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
  • Ohshima, S., & Seyama, A. (2016). Establishment of proliferative tetraploid cells from telomerase-immortalized normal human fibroblasts. Genes, Chromosomes and Cancer, 55(6), 522–530. https://doi.org/10.1002/gcc.22354
  • Chou, Y., Krupp, A., Kaynor, C., Gaudin, R., Ma, M., Cahir-McFarland, E., & Kirchhausen, T. (2016). Inhibition of JCPyV infection mediated by targeted viral genome editing using CRISPR/Cas9. Scientific Reports, 6(1). https://doi.org/10.1038/srep36921
  • Hayakawa, T., Fujita, F., Okada, F., & Sekiguchi, K. (2022). Establishment and characterization of immortalized sweat gland myoepithelial cells. Scientific reports, 12(1), 1-10. https://doi.org/10.1038/s41598-021-03991-5
  • 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
  • Othman, Ahmad H. The Role of Runx2 in Regulating Microtubule Stability. Rush University ProQuest Dissertations & Theses,  2021. 28318196.  Application: Cell Immortalization
  • Winogradzki, M., S.Patel, W.Holmes, A.Vistal, A.Othman, and J.Pratap. 2025. “The Role of Runx2 in Microtubule Dynamics and Its Effects on Osteoblast Migration.” Cytoskeleton1–19. https://doi.org/10.1002/cm.70064.  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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