pNAS1b split mCherry NEDD4-2 WW2
Purpose(Empty Backbone) Mode #2 phosphosite expression (split mCherry, using NEDD4-2 WW2 binding domain)
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||111883||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
- Backbone size (bp) 5500
Vector typeBacterial Expression
/ Fusion Protein
- Split mCherry system: NEDD4-2 WW2 fused to C-terminal split mCherry; phosphosite empty cassette fused to N-term split mCherry (N terminal on backbone)
Growth in Bacteria
Bacterial Resistance(s)Ampicillin, 100 μg/mL
- Cloning method Restriction Enzyme
Terms and Licenses
- Not Available to Industry
- Zeocin® is an InvivoGen trademark.
Backbone originally described in Sawyer, et al, Designed Phosphoprotein Recognition in Escherichia coli, 2014.
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:pNAS1b split mCherry NEDD4-2 WW2 was a gift from Jesse Rinehart (Addgene plasmid # 111883 ; http://n2t.net/addgene:111883 ; RRID:Addgene_111883)
For your References section:Encoding human serine phosphopeptides in bacteria for proteome-wide identification of phosphorylation-dependent interactions. Barber KW, Muir P, Szeligowski RV, Rogulina S, Gerstein M, Sampson JR, Isaacs FJ, Rinehart J. Nat Biotechnol. 2018 Aug;36(7):638-644. doi: 10.1038/nbt.4150. Epub 2018 Jun 11. 10.1038/nbt.4150 PubMed 29889213