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Addgene

pCS2-hSecurin
(Plasmid #32903)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 32903 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    pCS2+
  • Backbone manufacturer
    RZPD
  • Backbone size w/o insert (bp) 4000
  • Modifications to backbone
    Modified with N-term ZZ-Tev4 (two IgG binding domains of protein A (ZZ), followed by four TEV-protease cleavage sequences).
  • Vector type
    Mammalian Expression ; in vitro translation

Growth in Bacteria

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

Gene/Insert

  • Gene/Insert name
    Securin
  • Species
    H. sapiens (human)
  • Entrez Gene
    PTTG1 (a.k.a. EAP1, ECRAR, HPTTG, PTTG, TUTR1)
  • Promoter simian CMV IE94
  • Tag / Fusion Protein
    • ZZ-Tev4 (N terminal on backbone)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site none (unknown if destroyed)
  • 3′ cloning site none (unknown if destroyed)
  • 5′ sequencing primer CMV fwd
  • 3′ sequencing primer M13 reverse
  • (Common Sequencing Primers)

Terms and Licenses

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

Depositor Comments

N-terminal tag is two IgG binding domains of protein A (ZZ), followed by four TEV-protease cleavage sequences.

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:

    pCS2-hSecurin was a gift from Marc Kirschner (Addgene plasmid # 32903 ; http://n2t.net/addgene:32903 ; RRID:Addgene_32903)
  • For your References section:

    Dual inhibition of sister chromatid separation at metaphase. Stemmann O, Zou H, Gerber SA, Gygi SP, Kirschner MW. Cell. 2001 Dec 14;107(6):715-26. 10.1016/S0092-8674(01)00603-1 PubMed 11747808