Purpose(Empty Backbone) guide RNA (gRNA) expression vector used to create a gRNA to a specific sequence; uses T7 promoter for in vitro transcription
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||42250||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
|Cloning Grade DNA||42250-DNA.cg||2 µg of cloning grade DNA in Tris buffer||1||$95|
This material is available to academics and nonprofits only.
Backbone manufacturerJoung lab DR274
- Backbone size (bp) 2147
Vector typeWorm Expression, CRISPR ; zebrafish expression
- Promoter T7
Growth in Bacteria
Growth Strain(s)XL1 Blue
- Cloning method Unknown
- 5′ sequencing primer M13 forward (Common Sequencing Primers)
For more information on Joung Lab CRISPR Plasmids please refer to: http://www.addgene.org/crispr/jounglab/
Information for Cloning Grade DNA (Catalog # 42250-DNA.cg) ( Back to top )
Cloning grade DNA is suitable for use in PCR, cloning reactions, or transformation into E. coli. The purity and amount is not suitable for direct transfections.
- Amount 2 µg
- Guaranteed Concentration 100 ng/µl +/- 5 ng/µl
- Pricing $95 USD
- Storage DNA can be stored at 4℃ (short term) or -20℃ (long term).
Terms and Licenses
- Not Available to Industry
Addgene has verified this plasmid using Next Generation Sequencing. Results are available here
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:DR274 was a gift from Keith Joung (Addgene plasmid # 42250 ; http://n2t.net/addgene:42250 ; RRID:Addgene_42250)
For your References section:Efficient genome editing in zebrafish using a CRISPR-Cas system. Hwang WY, Fu Y, Reyon D, Maeder ML, Tsai SQ, Sander JD, Peterson RT, Yeh JR, Joung JK. Nat Biotechnol. 2013 Jan 29. doi: 10.1038/nbt.2501. 10.1038/nbt.2501 PubMed 23360964