|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||17618||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
Vector typeMammalian Expression, Lentiviral
Growth in Bacteria
- Cloning method Restriction Enzyme
- 5′ sequencing primer EF-1a forward (Common Sequencing Primers)
Terms and Licenses
- Not Available to Industry
Articles Citing this Plasmid
In a SIN LV containing the elongation factor 1alpha promoter, we included a PGK promoter that drives expression of GFP as a reporter. Dual-promoter LVs can coexpress multiple transgenes efficiently in a single target cell.
Recombinant LVs were produced by transient transfection of the transducing vector into 293T cells with two packaging vectors: pMD.G, a plasmid expressing the VSV-G envelope gene, and pCMVDeltaR8.91, a plasmid expressing the HIV-1 gag/pol, tat, and rev genes.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
For your Materials & Methods section:EF.PGK.GFP was a gift from Linzhao Cheng (Addgene plasmid # 17618 ; http://n2t.net/addgene:17618 ; RRID:Addgene_17618)
For your References section:Lentiviral vectors with two independent internal promoters transfer high-level expression of multiple transgenes to human hematopoietic stem-progenitor cells. Yu X, Zhan X, D'Costa J, Tanavde VM, Ye Z, Peng T, Malehorn MT, Yang X, Civin CI, Cheng L. Mol Ther. 2003 Jun . 7(6):827-38. 10.1016/S1525-0016(03)00104-7 PubMed 12788657