CJ34 (miR-1003 3'ssAG->GA)
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||17770||Standard format: Plasmid sent in bacteria as agar stab||1||$65|
This material is available to academics and nonprofits only.
Vector backbonepCaSpeR4-tubulin promoter
Backbone manufacturerCarl Thummel Lab
- Backbone size w/o insert (bp) 10200
Vector typeDrosophila P-element vector
Growth in Bacteria
Gene/Insert namedme-miR-1003 minigene 3'ssAG->GA
SpeciesD. melanogaster (fly)
Insert Size (bp)390
Mutationsplice site mutation
- Cloning method Restriction Enzyme
- 5′ cloning site KpnI (unknown if destroyed)
- 3′ cloning site NotI (unknown if destroyed)
- 5′ sequencing primer n/a (Common Sequencing Primers)
Terms and Licenses
Site-directed mutagenesis was used to make 3' splice site mutations with the indicated primers: CCTCTCACAT TTACATATTC ACGACGCCGT GAGCTGC and GCAGCTCACG GCGTCGTGAA TATGTAAATG TGAGAGG. pCaSpeR4 contains a ~2.4 kb tubulin promoter inserted between the EcoRI and KpnI sites.
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:CJ34 (miR-1003 3'ssAG->GA) was a gift from David Bartel (Addgene plasmid # 17770 ; http://n2t.net/addgene:17770 ; RRID:Addgene_17770)
For your References section:Intronic microRNA precursors that bypass Drosha processing. Ruby JG, Jan CH, Bartel DP. Nature. 2007 Jul 5. 448(7149):83-6. 10.1038/nature05983 PubMed 17589500
Map uploaded by the depositor.