pAAV-Ef1a-DIO C1V1 (t/t)-TS-mCherry
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||35498||Plasmid sent as bacteria in agar stab||1||$65|
This material is available to academics and nonprofits only.
- Backbone size w/o insert (bp) 5590
Modifications to backboneAddition of Ef1a promoter, Lox sites and a WPRE
Vector typeMammalian Expression, AAV
Growth in Bacteria
Copy numberHigh Copy
Gene/Insert nameChR1-VChR1 Chimera
Alt nameC1V1 (t/t)
Insert Size (bp)1809
MutationE122T and E162T
- Promoter Ef1a
/ Fusion Protein
- mCherry (C terminal on insert)
- Cloning method Restriction Enzyme
- 5′ cloning site AscI (not destroyed)
- 3′ cloning site NheI (not destroyed)
- 5′ sequencing primer CACCCACACAAAGGAAAAGGGCC
- 3′ sequencing primer GCAATAGCATGATACAAAGG (Common Sequencing Primers)
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:pAAV-Ef1a-DIO C1V1 (t/t)-TS-mCherry was a gift from Karl Deisseroth (Addgene plasmid # 35498)
For your References section:Neocortical excitation/inhibition balance in information processing and social dysfunction. Yizhar O, Fenno LE, Prigge M, Schneider F, Davidson TJ, O'Shea DJ, Sohal VS, Goshen I, Finkelstein J, Paz JT, Stehfest K, Fudim R, Ramakrishnan C, Huguenard JR, Hegemann P, Deisseroth K. Nature. 2011 Jul 27;477(7363):171-8. doi: 10.1038/nature10360. 10.1038/nature10360 PubMed 21796121
Generated by Addgene from full sequence supplied by depositor.
Map uploaded by the depositor.