pDONR-U6gRNA-PGKpuro2APDGFB
(Plasmid
#136409)
-
Purpose(Empty Backbone) Donor vector for gRNA subcloning. Required for gRNA cloning into the RCAS-DV. Also constitutively expresses PDGFB.
-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 136409 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepDONR-U6gRNA-PGKpuro2ABFP
-
Modifications to backboneBbsI restriction site in the PDGFB sequence (Glu173Asp174) was removed by site directed mutagenesis. HA tag on vector.
-
Vector typeCRISPR
-
Selectable markersPuromycin
Growth in Bacteria
-
Bacterial Resistance(s)Kanamycin, 50 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)NEB Stable
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameNone
-
MutationBbsI restriction site in the PDGFB sequence (Glu173Asp174) was removed by site directed mutagenesis
Cloning Information
- Cloning method Unknown
- 5′ sequencing primer Unknown (Common Sequencing Primers)
Resource Information
-
Supplemental Documents
-
Addgene Notes
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- 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:
pDONR-U6gRNA-PGKpuro2APDGFB was a gift from Massimo Squatrito (Addgene plasmid # 136409 ; http://n2t.net/addgene:136409 ; RRID:Addgene_136409) -
For your References section:
Somatic genome editing with the RCAS-TVA-CRISPR-Cas9 system for precision tumor modeling. Oldrini B, Curiel-Garcia A, Marques C, Matia V, Uluckan O, Grana-Castro O, Torres-Ruiz R, Rodriguez-Perales S, Huse JT, Squatrito M. Nat Commun. 2018 Apr 13;9(1):1466. doi: 10.1038/s41467-018-03731-w. 10.1038/s41467-018-03731-w PubMed 29654229