PurposeGeneral Purpose cloning vector for "INT"-like constructs under U6-promoter expression.
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||68433||Standard format: Plasmid sent in bacteria as agar stab||1||$65|
This material is available to academics and nonprofits only.
Vector typeMammalian Expression, CRISPR ; Cloning vector for generating INT-like constructs
Growth in Bacteria
Copy numberHigh Copy
Gene/Insert nameINT construct
gRNA/shRNA sequencegRNA: GATCTAGATACGACTCACTAT
- Promoter human U6
- Cloning method Restriction Enzyme
- 5′ cloning site Unknown (unknown if destroyed)
- 3′ cloning site Unknown (unknown if destroyed)
- 5′ sequencing primer LKO.1 5
- 3′ sequencing primer M13R (Common Sequencing Primers)
sgRNA targets the (ATCTAGATACGACTCACTAT) sequence in the Gluc reporter. Contains an internal cloning site into which "accessory domain," can be inserted. Cut with BbsI. More details outlined in the Online Methods section.
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:pU6_(Gluc)_INT(GenPurpClon) was a gift from John Rinn (Addgene plasmid # 68433 ; http://n2t.net/addgene:68433 ; RRID:Addgene_68433)
For your References section:Multiplexable, locus-specific targeting of long RNAs with CRISPR-Display. Shechner DM, Hacisuleyman E, Younger ST, Rinn JL. Nat Methods. 2015 Jul;12(7):664-70. doi: 10.1038/nmeth.3433. Epub 2015 Jun 1. 10.1038/nmeth.3433 PubMed 26030444