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Addgene

pEGFP-imp α
(Plasmid #119718)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 119718 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    pEGFP-ΔC2
  • Modifications to backbone
    pEGFP-delat C2 is constructed by ligation of blunt-ended HindIII site of pEGFP-C1, resulting in the C2-type reading frame
  • Vector type
    Mammalian Expression
  • Selectable markers
    Neomycin (select with G418)

Growth in Bacteria

  • Bacterial Resistance(s)
    Kanamycin, 50 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Copy number
    High Copy

Gene/Insert

  • Gene/Insert name
    importinα
  • Species
    H. sapiens (human)
  • Mutation
    contains amino acids 251-529
  • Entrez Gene
    KPNA2 (a.k.a. IPOA1, PTAC58, QIP2, RCH1, SRP1-alpha, SRP1alpha)
  • Promoter CMV
  • Tag / Fusion Protein
    • EGFP (N terminal on backbone)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site EcoRI (unknown if destroyed)
  • 3′ cloning site SalI (unknown if destroyed)
  • 5′ sequencing primer n/a
  • (Common Sequencing Primers)

Terms and Licenses

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

Depositor Comments

1-kb fragment of the EcoRI-XhoI fragment of DsRed-imp alpha (Addgene plasmid 119679) was cloned into the EcoRI-SalI sites of pEGFP-ΔC2, a frame-shifted derivative of pEGFP-C1.

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:

    pEGFP-imp α was a gift from Kenji Sugimoto (Addgene plasmid # 119718 ; http://n2t.net/addgene:119718 ; RRID:Addgene_119718)
  • For your References section:

    A rapid and simple method of evaluating the dimeric tendency of fluorescent proteins in living cells using a truncated protein of importin alpha as fusion tag. Nakagawa C, Nishimura S, Senda-Murata K, Sugimoto K. Biosci Biotechnol Biochem. 2012;76(2):388-90. doi: 10.1271/bbb.110677. Epub 2012 Feb 7. 10.1271/bbb.110677 PubMed 22313767