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Addgene

His8-TEV-PseH
(Plasmid #89725)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 89725 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    pET30b (+)
  • Backbone manufacturer
    EMB Biosciences
  • Backbone size w/o insert (bp) 5400
  • Total vector size (bp) 5874
  • Modifications to backbone
    Incorporation of N-terminal OctaHis tag and TEV cleavage site before insert
  • Vector type
    Bacterial Expression

Growth in Bacteria

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

Gene/Insert

  • Gene/Insert name
    PseH
  • Species
    Campylobacter jejuni
  • Insert Size (bp)
    474
  • GenBank ID
    905605
  • Entrez Gene
    pseH (a.k.a. Cj1313)
  • Tags / Fusion Proteins
    • 2xHis Gln 5xHis (N terminal on backbone)
    • TEV (N terminal on backbone)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site BamHI (unknown if destroyed)
  • 3′ cloning site XhoI (unknown if destroyed)
  • 5′ sequencing primer TTGATAAAACTTAAAAATTTCGCAGAACTTAATTCTCAAGAA
  • 3′ sequencing primer TTAGCTAGGCAAGGCTTTGCAGTGAGATTGCTTTAAGC
  • (Common Sequencing Primers)

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:

    His8-TEV-PseH was a gift from Barbara Imperiali (Addgene plasmid # 89725 ; http://n2t.net/addgene:89725 ; RRID:Addgene_89725)
  • For your References section:

    Chemoenzymatic Synthesis and Applications of Prokaryote-Specific UDP-Sugars. Zamora CY, Schocker NS, Chang MM, Imperiali B. Methods Enzymol. 2017;597:145-186. doi: 10.1016/bs.mie.2017.06.003. Epub 2017 Jul 5. 10.1016/bs.mie.2017.06.003 PubMed 28935101