-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 31483 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepCVL
- Backbone size w/o insert (bp) 5000
-
Vector typeLentiviral
-
Selectable markersPuromycin
Growth in Bacteria
-
Bacterial Resistance(s)Ampicillin, 100 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)NEB Stable
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameTraffic Light Reporter 2.1 (V2468 zfn target) EF Puro
-
Insert Size (bp)2939
-
MutationTraffic Light 2.0 series have a +3 PEST sequence that aids in degradation of the +3 "gibberishFP" produced by mutNHEJ events. The mCherry sequence has M9S and M16L mutations that reduce background fluorescence from internal start codons. This is what ".1" stands for.
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer n/a (Common Sequencing Primers)
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
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:
pCVL Traffic Light Reporter 2.1 (VF2468 ZFN target) Ef1a was a gift from Andrew Scharenberg (Addgene plasmid # 31483 ; http://n2t.net/addgene:31483 ; RRID:Addgene_31483) -
For your References section:
Tracking genome engineering outcome at individual DNA breakpoints. Certo MT, Ryu BY, Annis JE, Garibov M, Jarjour J, Rawlings DJ, Scharenberg AM. Nat Methods. 2011 Jul 10;8(8):671-6. doi: 10.1038/nmeth.1648. 10.1038/nmeth.1648 PubMed 21743461