PurposeTo overexpress PPARgamma1 in Mammalian Cells
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||78769||Standard format: Plasmid sent in bacteria as agar stab||1||$85|
This material is available to academics and nonprofits only.
Backbone manufacturerderived from pCS2+
Vector typeMammalian Expression
Growth in Bacteria
Bacterial Resistance(s)Ampicillin, 100 μg/mL
Copy numberHigh Copy
Alt nameisoform 1
SpeciesM. musculus (mouse)
Entrez GenePparg (a.k.a. Nr1c3, PPAR-gamma, PPAR-gamma2, PPARgamma, PPARgamma2)
- Promoter CMV IE94
/ Fusion Protein
- 3xFLAG (N terminal on backbone)
- Cloning method Restriction Enzyme
- 5′ cloning site unknown (unknown if destroyed)
- 3′ cloning site unknown (unknown if destroyed)
- 5′ sequencing primer SP6
- 3′ sequencing primer T7 (Common Sequencing Primers)
Articles Citing this Plasmid
Terms and Licenses
- Not Available to Industry
- Zeocin® is an InvivoGen trademark.
pCS4+ is based on pCS2+, with the following unique restriction endonuclease sites are added to MCS: BsrG1, EcoRV, AscI, NcoI, EcoO019, Sfi I, Fes I, Bgl II, Nhe I. A start codon with the Kozak sequence and stop codons in all three frames are added.
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:PCS4 3XFLAG-PPARgamma1 was a gift from Jaewhan Song (Addgene plasmid # 78769 ; http://n2t.net/addgene:78769 ; RRID:Addgene_78769)
For your References section:Suppression of PPARgamma through MKRN1-mediated ubiquitination and degradation prevents adipocyte differentiation. Kim JH, Park KW, Lee EW, Jang WS, Seo J, Shin S, Hwang KA, Song J. Cell Death Differ. 2014 Apr;21(4):594-603. doi: 10.1038/cdd.2013.181. Epub 2013 Dec 13. 10.1038/cdd.2013.181 PubMed 24336050