-
PurposeLentiviral EOS reporter with Oct3/4 enhancer (x3), expresses EGFP and Puro resistance
-
Depositing Lab
-
Publication
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 21313 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonePL-SIN lentiviral vector
-
Backbone manufacturerBuzina et al., PLoS Genetics, 2008
- Backbone size w/o insert (bp) 6141
-
Vector typeMammalian Expression, Lentiviral
-
Selectable markersPuromycin
Growth in Bacteria
-
Bacterial Resistance(s)Ampicillin, 100 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)Stbl3
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameEnhanced Green Fluorescence Protein, Puromycin resistance gene
-
Alt nameEGFP-IRES-Puro
-
Insert Size (bp)1947
- Promoter EOS-C(3+) promoter region
Cloning Information
- Cloning method Unknown
- 5′ sequencing primer n/a
- 3′ sequencing primer n/a (Common Sequencing Primers)
Resource Information
-
Articles Citing this Plasmid
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
EGFP and Puro resistance genes driven by EOS-C(3+) promoter. PL-SIN lentiviral vector (Buzina et al., PLoS Genetics, 2008) requires Tat cDNA for lentivirus production, as well as other packaging cDNAs (Gag/pol, Rev, and VSV-G).
The construct PL-SIN-EOS-C(3+)-EiP is the same as PL-EOS-C(3+)-EGFP-IRES-PuroR (EiP = EGFP-IRES-PuroR).
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:
PL-SIN-EOS-C(3+)-EiP was a gift from James Ellis (Addgene plasmid # 21313 ; http://n2t.net/addgene:21313 ; RRID:Addgene_21313) -
For your References section:
Isolation of human iPS cells using EOS lentiviral vectors to select for pluripotency. Hotta A, Cheung AY, Farra N, Vijayaragavan K, Seguin CA, Draper JS, Pasceri P, Maksakova IA, Mager DL, Rossant J, Bhatia M, Ellis J. Nat Methods. 2009 May . 6(5):370-6. 10.1038/nmeth.1325 PubMed 19404254