LUC2 (L/Sec/deltaP)
(Plasmid
#112145)
-
PurposeMammalian expression vector to test the effect of substituting selenocysteine for Cys on luciferase enzyme activity
-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 112145 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepcDNA3.1
-
Vector typeMammalian Expression
Growth in Bacteria
-
Bacterial Resistance(s)Ampicillin, 100 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameLuciferase coding region with Cysteine 258 mutated to selenocysteine (U) and deleted AUGA in PHGPx SECIS core
-
SpeciesR. norvegicus (rat); Photinus pyralis
-
MutationCysteine 258 mutated to selenocysteine (U) and deleted AUGA PHGPx SECIS
-
Entrez GeneGpx4 (a.k.a. Gshpx-4, Phgpx, gpx-4, snGpx)
Cloning Information
- Cloning method TOPO Cloning
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
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:
LUC2 (L/Sec/deltaP) was a gift from Paul Copeland (Addgene plasmid # 112145 ; http://n2t.net/addgene:112145 ; RRID:Addgene_112145) -
For your References section:
Efficiency of mammalian selenocysteine incorporation. Mehta A, Rebsch CM, Kinzy SA, Fletcher JE, Copeland PR. J Biol Chem. 2004 Sep 3;279(36):37852-9. doi: 10.1074/jbc.M404639200. Epub 2004 Jun 30. 10.1074/jbc.M404639200 PubMed 15229221