sgRNA BRCA1 Q1779Stop
PurposePlasmid expressing a sgRNA to introduce BRCA1 Q1779Stop using base editing
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||139331||Standard format: Plasmid sent in bacteria as agar stab||1||$75|
This material is available to academics and nonprofits only.
Vector backboneB52 (Addgene #100708)
- Backbone size w/o insert (bp) 2633
- Total vector size (bp) 2637
Modifications to backboneInsertion of the sgRNA at the BbsI cloning site. The BsmBI cloning site is still available to express a second sgRNA.
Vector typeMammalian Expression
Growth in Bacteria
Gene/Insert namesgRNA to insert BRCA1 Q1779Stop using base editing
Alt namesgRNA sequence: TTAGATCAACTGGAATGGA
SpeciesH. sapiens (human)
Insert Size (bp)19
- Promoter U6
- Cloning method Restriction Enzyme
- 5′ cloning site BbsI (destroyed during cloning)
- 3′ cloning site BbsI (destroyed during cloning)
- 5′ sequencing primer GAGGTACCTCGAGGAATTCTCTAGA (Common Sequencing Primers)
Terms and Licenses
- Not Available to Industry
- Zeocin® is an InvivoGen trademark.
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:sgRNA BRCA1 Q1779Stop was a gift from Alberto Ciccia (Addgene plasmid # 139331 ; http://n2t.net/addgene:139331 ; RRID:Addgene_139331)
For your References section:Detection of Marker-Free Precision Genome Editing and Genetic Variation through the Capture of Genomic Signatures. Billon P, Nambiar TS, Hayward SB, Zafra MP, Schatoff EM, Oshima K, Dunbar A, Breinig M, Park YC, Ryu HS, Tschaharganeh DF, Levine RL, Baer R, Ferrando A, Dow LE, Ciccia A. Cell Rep. 2020 Mar 10;30(10):3280-3295.e6. doi: 10.1016/j.celrep.2020.02.068. 10.1016/j.celrep.2020.02.068 PubMed 32160537