|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||24359||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) 9100
Vector typeInsect Expression
Growth in Bacteria
Insert Size (bp)2260
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (unknown if destroyed)
- 3′ cloning site BamHI (unknown if destroyed)
- 5′ sequencing primer FLP-rec, pCasper-F (Common Sequencing Primers)
FLPo from Addgene plasmid 13792 was PCR amplified to include EcoRI/XbaI restriction sites, and cloned into pQUAS-DSCP to generate pQUAS-DSCP-FLPo. QUAS-DSCP-FLPo-SV40 was excised from pQUAS-DSCP-FLPo by BamHI digestion, and subcloned into pCa4B2G at BamHI.
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:pCa4B2G-QUAS-DSCP-FLPo was a gift from Liqun Luo (Addgene plasmid # 24359 ; http://n2t.net/addgene:24359 ; RRID:Addgene_24359)
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