CYP2C9 in vector pCW ori+
PurposeModification of CYP2C9 and 2C19 s for bacterial expression
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||69554||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) 5500
Vector typeBacterial Expression
Growth in Bacteria
Copy numberHigh Copy
SpeciesH. sapiens (human)
Entrez GeneCYP2C9 (a.k.a. CPC9, CYP2C, CYP2C10, CYPIIC9, P450-2C9, P450IIC9)
- Cloning method Restriction Enzyme
- 5′ cloning site NdeI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer pCW-SEQ-fwd (5'ACATCGTATAACGTTACTGG-3')
- 3′ sequencing primer pCW-SEQ-rev (5'-CTTTCGTCTTCAAGCAGATCTG-3') (Common Sequencing Primers)
Terms and Licenses
- Not Available to Industry
Modification of CYP2C9 for bacterial expression as per Barnes et al. PNAS 88:5597, 1991 [PMID: 1829523]: First 8 amino acids of CYP2C cDNAs replaced with those of bovine 17α hydroxylase (MALLLAVF) to optimize bacterial expression.
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:CYP2C9 in vector pCW ori+ was a gift from Joyce Goldstein (Addgene plasmid # 69554 ; http://n2t.net/addgene:69554 ; RRID:Addgene_69554)