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Addgene

YIplac211-SEC7-mCherry2Bx6
(Plasmid #105267)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 105267 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    YIplac211
  • Backbone size w/o insert (bp) 3797
  • Total vector size (bp) 10410
  • Vector type
    Yeast Expression
  • Selectable markers
    URA3

Growth in Bacteria

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

Gene/Insert

  • Gene/Insert name
    Sec7 portion
  • Species
    S. cerevisiae (budding yeast)
  • Entrez Gene
    SEC7 (a.k.a. YDR170C)
  • Tag / Fusion Protein
    • mCherry2Bx6 (C terminal on insert)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site EcoRI (not destroyed)
  • 3′ cloning site SphI (not destroyed)
  • 5′ sequencing primer M13 FORWARD
  • 3′ sequencing primer M13 REVERSE
  • (Common Sequencing Primers)

Resource Information

Terms and Licenses

Trademarks:
  • Zeocin® is an InvivoGen trademark.

Depositor Comments

Addgene's quality control identified a frameshift at Q266 of URA3. The depositing lab states that this mutation should not affect selection.

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:

    YIplac211-SEC7-mCherry2Bx6 was a gift from Benjamin Glick (Addgene plasmid # 105267 ; http://n2t.net/addgene:105267 ; RRID:Addgene_105267)
  • For your References section:

    Budding Yeast Has a Minimal Endomembrane System. Day KJ, Casler JC, Glick BS. Dev Cell. 2018 Jan 8;44(1):56-72.e4. doi: 10.1016/j.devcel.2017.12.014. Epub 2018 Jan 8. 10.1016/j.devcel.2017.12.014 PubMed 29316441