Ordering
Item | Catalog # | Description | Quantity | Price (USD) | ||
---|---|---|---|---|---|---|
Plasmid | 89745 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $75 | Add to Cart |
This material is available to academics and nonprofits only.
Backbone
- Vector backbonepLuc-C1(Search Vector Database)
- Backbone manufacturerDerived by our lab using pExFP-C1 and pGL3
- Backbone sizew/o insert(bp)5673
- Total vector size (bp)6119
- Vector typeMammalian Expression, Luciferase
- Selectable markersNeomycin (select with G418)
Growth in Bacteria
- Bacterial Resistance(s)Kanamycin
- Growth Temperature37°C
- Growth Strain(s)DH5alpha
- Copy numberHigh Copy
Gene/Insert
- Gene/Insert nameOptoJNKi dark-state mutant
- Alt nameAsLov2Jalpha (404-546)-C450A-JIP11
- SpeciesSynthetic; Avena Sativa and
- Insert Size (bp)478
- MutationC450A mutation of AsLov2Jalpha
- GenBank IDKY595941
- PromoterCMV
- Tag/ Fusion Protein
- Firefly luciferase (N terminal on backbone)
Cloning Information
- Cloning methodRestriction Enzyme
- 5′ cloning siteEcoRI(not destroyed)
- 3′ cloning siteBamHI(not destroyed)
- 5′ sequencing primerluc2131+
- 3′ sequencing primerfastbac reverse (Common Sequencing Primers)
Resource Information
- A portion of this plasmid was derived from a plasmid made byWe designed and assembled the insert from de novo synthesised sequences
- Terms and Licenses
- UBMTA
- Luciferase Limited Use Label License
- Industry Terms
- Not Available to Industry
Depositor Comments
Please seeMelero-Fernandez de Mera RM*, Li LL*, Popinigis A, Cisek K, Tuittila M, Yadav L, Serva A, Courtney MJ (2017) A simple optogenetic MAPK inhibitor design reveals resonance between transcription-regulating circuitry and temporally-encoded inputs. Nat. Commun. 8, 15017 doi: 10.1038/ncomms15017 in press.