Purpose(Empty Backbone) shRNA silencing plasmid with eGFP transfection marker
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||52675||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
Backbone manufacturerLife Technologies
Modifications to backboneeGFP and its cytomegalovirus promoter from pEGFP-C3 were cloned into the KpnI site upstream of the U6 promoter within the pSilencer™ vector.
- Promoter CMV and U6
/ Fusion Protein
- CMV-EGFP (N terminal on backbone)
Growth in Bacteria
- Cloning method Restriction Enzyme
- 5′ sequencing primer EGFP-C
- 3′ sequencing primer M13-R (Common Sequencing Primers)
Terms and Licenses
- Not Available to Industry
EGFP is a transfection marker, not a fusion.
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:pSIL-eGFP was a gift from Johannes Hell (Addgene plasmid # 52675 ; http://n2t.net/addgene:52675 ; RRID:Addgene_52675)
For your References section:The cytoskeletal protein alpha-actinin regulates acid-sensing ion channel 1a through a C-terminal interaction. Schnizler MK, Schnizler K, Zha XM, Hall DD, Wemmie JA, Hell JW, Welsh MJ. J Biol Chem. 2009 Jan 30;284(5):2697-705. doi: 10.1074/jbc.M805110200. Epub 2008 Nov 21. 10.1074/jbc.M805110200 PubMed 19028690