Purpose(Empty Backbone) Retroviral vector for cloning and expressing your gene of interest. Zeocin selection.
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||1766||Plasmid sent as bacteria in agar stab||1||$65|
This material is available to academics and nonprofits only.
- Backbone size (bp) 4888
Vector typeMammalian Expression, Retroviral
Growth in Bacteria
Copy numberHigh Copy
- Cloning method Restriction Enzyme
- 5′ sequencing primer pBABE 5'
- 3′ sequencing primer pBABE 3' (Common Sequencing Primers)
Please acknowledge Jay Morgenstern and Hartmut Land and cite the following article if you use this plasmid in a publication:
Morgenstern JP, Land H., 1990, Nucleic Acids Research 18(12):3587-96.
SspI site in Amp gene.
If you are using the pBABE protocol from the Weinberg Lab to generate virus, please note that the Weinberg Lab recommends using pUMVC (Addgene #8449) and VSV-G (#8454) for packaging. The pCL-Eco plasmid listed in their protocol should be substituted with pUMVC.
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:pBABE-zeo (pBABE-bleo) was a gift from Hartmut Land & Jay Morgenstern & Bob Weinberg (Addgene plasmid # 1766)
For your References section:Advanced mammalian gene transfer: high titre retroviral vectors with multiple drug selection markers and a complementary helper-free packaging cell line. Morgenstern JP, Land H. Nucleic Acids Res. 1990 Jun 25;18(12):3587-96. PubMed 2194165