Lentiviral Packaging System

Pantropic Lentiviral Packaging System
  • Significantly reduced homology compared to other 3rd generation expression systems for added safety
  • Vectors provided individually to allow optimization of vector ratio
  • Contains three packaging plasmids (Rev, gag-pol, and VSVG) for use with your own third generation lentiviral transfer vector

 

Frequently Asked Questions about this product

General FAQs about Viral Gene Delivery

Email To BuyerPrint this PageCopy Link
Ordering

Please contact your distributor for pricing.

ViraSafe™ Lentivirus Packaging System, Pantropic
Catalog Number
VPK-206
Size
1 kit
Detection
N/A
Manual/Data Sheet Download
SDS Download
Map Download
Sequence Download
Price
$780.00
Product Details

Our ViraSafe™ Lentiviral Packaging Systems contain three packaging plasmids for co-transfection with your own third generation lentiviral expression construct. If you need an expression vector as well as the packaging plasmids, consider our ViraSafe™ Lentiviral Expression Complete Systems.

The Pantropic Packaging System assembles VSVG-pseudotyped lentiviruses which can easily infect virtually any cells regardless of their species of origin.

Recent Product Citations
  1. Han, S.J. et al. (2022). Steroid receptor coactivator-3 inhibition generates breast cancer antitumor immune microenvironment. Breast Cancer Res. 24(1):73. doi: 10.1186/s13058-022-01568-2.
  2. Moy, R.H. et al. (2022). Functional genetic screen identifies ITPR3/calcium/RELB axis as a driver of colorectal cancer metastatic liver colonization. Dev Cell. 57(9):1146-1159.e7. doi: 10.1016/j.devcel.2022.04.010.
  3. Banerjee, D. et al. (2021). A non-canonical, interferon-independent signaling activity of cGAMP triggers DNA damage response signaling. Nat Commun. 12(1):6207. doi: 10.1038/s41467-021-26240-9.
  4. Huna, A. et al. (2021). Loss of the Metastasis Suppressor NME1, But Not of Its Highly Related Isoform NME2, Induces a Hybrid Epithelial–Mesenchymal State in Cancer Cells. Int. J. Mol. Sci. 22(7):3718. doi: 10.3390/ijms22073718.
  5. Xie, W. et al. (2021). Pterostilbene accelerates wound healing by modulating diabetes-induced estrogen receptor β suppression in hematopoietic stem cells. Burns Trauma. doi: 10.1093/burnst/tkaa045.
  6. Low, J.L. et al. (2021). A chemical genetic screen identifies Aurora kinases as a therapeutic target in EGFR T790M negative, gefitinib-resistant head and neck squamous cell carcinoma (HNSCC). EBioMedicine. 64:103220. doi: 10.1016/j.ebiom.2021.103220.
  7. Tavora, B. et al. (2020). Tumoural activation of TLR3-SLIT2 axis in endothelium drives metastasis. Nature. doi: 10.1038/s41586-020-2774-y.
  8. Madan, E. et al. (2019). HIF-transcribed p53 chaperones HIF-1α. Nucleic Acids Res. pii: gkz766. doi: 10.1093/nar/gkz766.
  9. Madan, E. et al. (2019). Flower isoforms promote competitive growth in cancer. Nature. doi: 10.1038/s41586-019-1429-3.
  10. Aldi, S. et al. (2019). Dual roles of heparanase in human carotid plaque calcification. Atherosclerosis. 283:127-136. doi: 10.1016/j.atherosclerosis.2018.12.027.
  11. Guan, Y. et al. (2018). HMGB1 promotes the starvation-induced autophagic degradation of α-synuclein in SH-SY5Y cells Atg 5-dependently. Life Sci. 202:1-10. doi: 10.1016/j.lfs.2018.03.031.
  12. Kim, S.C. et al. (2018). Establishment and Characterization of Paired Primary and Peritoneal Seeding Human Colorectal Cancer Cell Lines: Identification of Genes That Mediate Metastatic Potential. Transl Oncol. 11(5):1232-1243. doi: 10.1016/j.tranon.2018.07.014.
  13. Z.-X. Liao, I. et al. (2018). Micro-scale RNA Interference using Iron Oxide Nanoparticle-modified Lentivirus. ChemNanoMat. 4(1): 98-102.
  14. Urakami, A. et al. (2017). Development of a novel virus-like particle vaccine platform that mimics immature form of alphavirus. Clin. Vaccine Immunol. doi: 10.1128/CVI.00090-17.
  15. Qiu, Y. et al. (2017). RhoA inhibits the hypoxia-induced apoptosis in osteoblasts. Int. J. Clin. Exp. Med. 10(4):6568-6576.
  16. Nguyen, A. et al. (2016). PKLR promotes colorectal cancer liver colonization through induction of glutathione synthesis. J Clin Invest. doi:10.1172/JCI83587.
  17. Vogt, J. et al. (2014). Protein Associated with SMAD1 (PAWS1/FAM83G) is a Substrate for Type I Bone Morphogenetic Protein Receptors and Modulates Bone Morphogenetic Protein Signalling. Open Bio. 4:130210.