|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||24385||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) 9000
Vector typeInsect Expression
Growth in Bacteria
Insert Size (bp)3000
- Cloning method Restriction Enzyme
- 5′ sequencing primer GFP-F (Common Sequencing Primers)
Terms and Licenses
- Not Available to Industry
The FRT-stop-FRT cassette, with additional BglII/NotI restriction sites, was PCR amplified from genomic DNA of UAS-FRT-stop-FRT-shibire (ts) flies and cloned into pUAST-mCD8-gfp to generate pUAST-FRT-stop-FRT-mCD8-gfp (pUAS>stop>mCD8-GFP)
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:pUAST>stop>mCD8-GFP was a gift from Liqun Luo (Addgene plasmid # 24385 ; http://n2t.net/addgene:24385 ; RRID:Addgene_24385)
For your References section:The Q System: A Repressible Binary System for Transgene Expression, Lineage Tracing, and Mosaic Analysis. Potter CJ, Tasic B, Russler EV, Liang L, Luo L.. Volume 141, Issue 3, 536-548, 30 April 2010 10.1016/j.cell.2010.02.025 PubMed 20434990