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Addgene

CelTag Plasmid
(Plasmid #66562)

Ordering

Item Catalog # Description Quantity Price (USD)
Plasmid 66562 Standard format: Plasmid sent in bacteria as agar stab 1 $85

This material is available to academics and nonprofits only.

Backbone

  • Vector backbone
    pGEM®-T Easy Vector
  • Backbone manufacturer
    Promega
  • Backbone size w/o insert (bp) 3015
  • Total vector size (bp) 5573
  • Modifications to backbone
    Addition of CelTag and cloNat resistance.
  • Vector type
    Bacterial Expression
  • Selectable markers
    Nourseothricin (cloNat)

Growth in Bacteria

  • Bacterial Resistance(s)
    Ampicillin, 100 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Growth instructions
    Ampicillin selection is sufficient for plasmid preparation. Nourseothricin selection is used to confirm insertion of the CelTag
  • Copy number
    Unknown

Gene/Insert

  • Gene/Insert name
    CelTag
  • Species
    S. cerevisiae (budding yeast)
  • Insert Size (bp)
    2558

Resource Information

  • A portion of this plasmid was derived from a plasmid made by
    The 13x myc epitope repeat and cloNat resistance gene were obtained from the pFA6a-13myc-natMX6 plasmid (gift from Dr. Antony Carr at University of Sussex), and the CBM3 was obtained from the pCIG plasmid (gift from Dr. Jiong Hong at Virginia Polytechnic Institute and State University)

Terms and Licenses

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

    CelTag Plasmid was a gift from David Engelke (Addgene plasmid # 66562 ; http://n2t.net/addgene:66562 ; RRID:Addgene_66562)
  • For your References section:

    A Novel Recombinant DNA System for High Efficiency Affinity Purification of Proteins in Saccharomyces cerevisiae. Carrick BH, Hao L, Smaldino PJ, Engelke DR. G3 (Bethesda). 2015 Dec 29. pii: g3.115.025106. doi: 10.1534/g3.115.025106. 10.1534/g3.115.025106 PubMed 26715090
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