-
Depositing Lab
-
Depositing OrganizationUniversity of Manchester
Located in United Kingdom of Great Britain and Northern Ireland -
Citations
-
Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 41432 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
| DNA | 41432-D50 | 50 μg of DNA in Tris buffer | $495 | ||
| DNA | 41432-D100 | 100 μg of DNA in Tris buffer | $585 | ||
Backbone
-
Vector backbonepcDNA3.1
-
Backbone manufacturerInvitrogen
- Backbone size w/o insert (bp) 5347
- Total vector size (bp) 6373
-
Modifications to backboneAn HpaI recognition site was introduced 34 bases downstream of the CMV promoter region in the pcDNA3.1 backbone to enable cloning in of 5' blunted inserts (e.g. JellyOp).
-
Vector typeMammalian Expression
-
Selectable markersNeomycin (select with G418)
Growth in Bacteria
-
Bacterial Resistance(s)Ampicillin, 100 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)XL1 Blue
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameBox jellyfish opsin
-
Alt nameJellyOp
-
SpeciesCarybdea rastonii
-
Insert Size (bp)1026
-
GenBank IDAB435549
- Promoter CMV
-
Tag
/ Fusion Protein
- 1D4 epitope at 3' end (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HpaI (destroyed during cloning)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer M13 F
- 3′ sequencing primer M13 R
- (Common Sequencing Primers)
Resource Information
-
A portion of this plasmid was derived from a plasmid made byThis gene was synthesised by Genscript Corp at our request and provided in a puc57 cloning vector, from which our lab constructed this pcDNA3.1 JellyOp plasmid.
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
The original JellyOp gene from which we designed this coding region with a 1D4 fusion was sequenced by Koyanagi et al (2008). PNAS 105:15576-15580.
DNA (Catalog # 41432-D50)
Purpose
Ready-to-use, high-purity DNA prep. DNA aliquots are suitable for use in mammalian cell transfections and other molecular biology applications.
Delivery
- Amount 50 μg
- Concentration 1 μg/μL
- Pricing $495 USD
- Storage 4 ℃ (short-term) or -20 ℃ (long-term)
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Quality Control
Every DNA prep is verified by next-generation sequencing, confirming plasmid identity, sequence integrity, and absence of DNA contaminants. Concentration is confirmed to be within ±2.5% of the stated concentration.
Our production process has been validated to consistently yield endotoxin levels below 1.0 EU/μg. Individual lots are not tested for endotoxin.
DNA (Catalog # 41432-D100)
Purpose
Ready-to-use, high-purity DNA prep. DNA aliquots are suitable for use in mammalian cell transfections and other molecular biology applications.
Delivery
- Amount 100 μg
- Concentration 1 μg/μL
- Pricing $585 USD
- Storage 4 ℃ (short-term) or -20 ℃ (long-term)
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Quality Control
Every DNA prep is verified by next-generation sequencing, confirming plasmid identity, sequence integrity, and absence of DNA contaminants. Concentration is confirmed to be within ±2.5% of the stated concentration.
Our production process has been validated to consistently yield endotoxin levels below 1.0 EU/μg. Individual lots are not tested for endotoxin.
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:
pcDNA3.1 JellyOp was a gift from Robert Lucas (Addgene plasmid # 41432 ; http://n2t.net/addgene:41432 ; RRID:Addgene_41432) -
For your References section:
Reproducible and sustained regulation of Galphas signalling using a metazoan opsin as an optogenetic tool. Bailes HJ, Zhuang LY, Lucas RJ. PLoS One. 2012;7(1):e30774. Epub 2012 Jan 24. 10.1371/journal.pone.0030774 PubMed 22292038