-
Purpose(Empty Backbone) multicopy (YEp) vector with a LYS2 marker and a 2-μm origin of replication
-
Depositing Lab
-
Publication
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 51787 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepRS423
-
Modifications to backboneThe CEN plasmid pRS327 was constructed by homology mediated recombination in yeast. A 1.84-kb ApaLI fragment from pRS423 that has the 2-μm origin of replication was transformed into lys2 yeast along with plasmid pRS307 that had been linearized with AatII. Selection for Lys+ prototrophs identified yeast where recombination of the homologous regions between the two plasmids created a circular DNA molecule with the 2-μm origin of DNA replication and the LYS2 marker.
-
Vector typeYeast Expression
-
Selectable markersLYS2
Growth in Bacteria
-
Bacterial Resistance(s)Ampicillin, 100 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberUnknown
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer M13-F20
- 3′ sequencing primer M13R (Common Sequencing Primers)
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:
pRS327 was a gift from David Stillman (Addgene plasmid # 51787 ; http://n2t.net/addgene:51787 ; RRID:Addgene_51787) -
For your References section:
pRS yeast vectors with a LYS2 marker. Eriksson P, Thomas LR, Thorburn A, Stillman DJ. Biotechniques. 2004 Feb;36(2):212-3. 10.2144/04362BM01 PubMed 14989082