|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||31034||Plasmid sent as bacteria in agar stab||1||$65|
This material is available to academics and nonprofits only.
- Backbone size w/o insert (bp) 5582
Growth in Bacteria
Bacterial Resistance(s)Ampicillin (50 ug/ml)
Copy numberHigh Copy
Gene/Insert nameTALEN-FokI nuclease backbone
Insert Size (bp)1948
/ Fusion Proteins
- FokI nuclease (C terminal on insert)
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer TEF_seq (ggtcttcaatttctcaagtttc) TAL_F1 (ttggcgtcggcaaacagtgg)
- 3′ sequencing primer homodimer_rev (aattcagatttcactagctg) TAL_R2 (ggcgacgaggtggtcgttg (Common Sequencing Primers)
Expression of the TAL-FokI homodimer in yeast.
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:pTAL3 was a gift from Adam Bogdanove & Daniel Voytas (Addgene plasmid # 31034)
For your References section:Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting. Cermak T, Doyle EL, Christian M, Wang L, Zhang Y, Schmidt C, Baller JA, Somia NV, Bogdanove AJ, Voytas DF. Nucleic Acids Res. 2011 Apr 14. ():. 10.1093/nar/gkr218 PubMed 21493687