Skip to main content
This website uses cookies to ensure you get the best experience. By continuing to use this site, you agree to the use of cookies.

Please note: Your browser does not support the features used on Addgene's website. You may not be able to create an account or request plasmids through this website until you upgrade your browser. Learn more

Please note: Your browser does not fully support some of the features used on Addgene's website. If you run into any problems registering, depositing, or ordering please contact us at [email protected]. Learn more

Addgene

pZA-mCherry-R5
(Plasmid #106258)

Full plasmid sequence is not available for this item.

Ordering

Item Catalog # Description Quantity Price (USD)
Plasmid 106258 Standard format: Plasmid sent in bacteria as agar stab 1 $85

This material is available to academics and nonprofits only.

Backbone

  • Vector backbone
    pZA31
  • Backbone manufacturer
    expressys
  • Backbone size w/o insert (bp) 2268
  • Total vector size (bp) 3078
  • Vector type
    Bacterial Expression

Growth in Bacteria

  • Bacterial Resistance(s)
    Chloramphenicol, 25 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Copy number
    Low Copy

Gene/Insert

  • Gene/Insert name
    mCherry
  • Alt name
    mCherry fluorescent protein
  • Insert Size (bp)
    810
  • Tag / Fusion Protein
    • Added silaffin R5 peptide to C terminus of mCherry after GGGGS linker (C terminal on insert)

Resource Information

Terms and Licenses

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:

    pZA-mCherry-R5 was a gift from Urartu Seker (Addgene plasmid # 106258 ; http://n2t.net/addgene:106258 ; RRID:Addgene_106258)
  • For your References section:

    Autonomous Synthesis of Fluorescent Silica Biodots Using Engineered Fusion Proteins. Olmez TT, Yuca E, Eyupoglu E, Catalak HB, Sahin O, Seker UOS. ACS Omega. 2018 Jan 31;3(1):585-594. doi: 10.1021/acsomega.7b01769. Epub 2018 Jan 18. 10.1021/acsomega.7b01769 PubMed 30023783