|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||26031||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
- Backbone size w/o insert (bp) 2946
Vector typeEntry vector
Growth in Bacteria
Copy numberHigh Copy
Insert Size (bp)710
- Cloning method Gateway Cloning
- 5′ cloning site attR2 (not destroyed)
- 3′ cloning site attL3 (not destroyed)
- 5′ sequencing primer M13pUC-fwd
- 3′ sequencing primer M13rev (Common Sequencing Primers)
Terms and Licenses
- Not Available to Industry
Articles Citing this Plasmid
"p3E" refers to 3' entry clones flanked by R2-L3.
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:543-p3E-2A-mcherrypA was a gift from Nathan Lawson (Addgene plasmid # 26031 ; http://n2t.net/addgene:26031 ; RRID:Addgene_26031)
For your References section:A truncation allele in vascular endothelial growth factor c reveals distinct modes of signaling during lymphatic and vascular development. Villefranc JA, Nicoli S, Bentley K, Jeltsch M, Zarkada G, Moore JC, Gerhardt H, Alitalo K, Lawson ND. Development. 2013 Apr;140(7):1497-506. doi: 10.1242/dev.084152. Epub 2013 Mar 5. 10.1242/dev.084152 PubMed 23462469