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pRSII308
(Plasmid #35443)

Ordering

Item Catalog # Description Quantity Price (USD)
Plasmid 35443 Standard format: Plasmid sent in bacteria as agar stab 1 $85

This material is available to academics and nonprofits only.

Backbone

  • Vector backbone
    pRS30x
  • Backbone manufacturer
    Stratagene
  • Backbone size (bp) 4516
  • Vector type
    Yeast integrating vector
  • Promoter None
  • Selectable markers
    ADE1

Growth in Bacteria

  • Bacterial Resistance(s)
    Ampicillin, 100 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Copy number
    High Copy

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ sequencing primer M13 Forward, T7
  • 3′ sequencing primer M13 Reverse
  • (Common Sequencing Primers)

Resource Information

  • A portion of this plasmid was derived from a plasmid made by
    Daniel J Lew, Duke University Chandra Tucker, Duke University (now at University of Colorado, Denver) M. Henar Valdivieso, Scripps Institutue (now at Institute of Biochemical Microbiology, Spain).

Terms and Licenses

  • Academic/Nonprofit Terms
  • Industry Terms
    • Not Available to Industry
Trademarks:
  • Zeocin® is an InvivoGen trademark.

Depositor Comments

ADE1 has been modified to remove BamHI, EcoRI, SalI and XbaI sites without altering the amino acid sequence of the Ade1 protein.

Note that there may be some small discrepancies between Addgene's quality control sequence and the the assembled from the depositor. These discrepancies are not in critical regions.

How to cite this plasmid ( Back to top)

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:

    pRSII308 was a gift from Steven Haase (Addgene plasmid # 35443 ; http://n2t.net/addgene:35443 ; RRID:Addgene_35443)
  • For your References section:

    New and Redesigned pRS Plasmid Shuttle Vectors for Genetic Manipulation of Saccharomycescerevisiae. Chee MK, Haase SB. G3 (Bethesda). 2012 May;2(5):515-26. Epub 2012 May 1. 10.1534/g3.111.001917 PubMed 22670222