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pMHBAD14
(Plasmid #42304)

Ordering

Item Catalog # Description Quantity Price (USD)
Plasmid 42304 Standard format: Plasmid sent in bacteria as agar stab 1 $85

This material is available to academics and nonprofits only.

Backbone

  • Vector backbone
    pBAD
  • Backbone manufacturer
    Invitrogen
  • Backbone size w/o insert (bp) 4786
  • Total vector size (bp) 4909
  • Vector type
    Bacterial Expression

Growth in Bacteria

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

Gene/Insert

  • Gene/Insert name
    NpuDnaE C-intein
  • Alt name
    C-intein of native split NpuDnaE
  • Alt name
    split intein
  • Species
    Nostoc punctiforme
  • Insert Size (bp)
    123
  • Promoter araBAD
  • Tag / Fusion Protein
    • GB1-H6 (C terminal on backbone)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site NdeI (not destroyed)
  • 3′ cloning site KpnI (not destroyed)
  • 5′ sequencing primer pBAD Forward
  • 3′ sequencing primer pBAD Reverse
  • (Common Sequencing Primers)

Resource Information

Terms and Licenses

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

Depositor Comments

There are 2 mismatches between Addgene's quality control and depositor's reference sequence. These changes are in backbone region and should not affect function.

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:

    pMHBAD14 was a gift from Hideo Iwai (Addgene plasmid # 42304 ; http://n2t.net/addgene:42304 ; RRID:Addgene_42304)
  • For your References section:

    Solution structure of DnaE intein from Nostoc punctiforme: structural basis for the design of a new split intein suitable for site-specific chemical modification. Oeemig JS, Aranko AS, Djupsjobacka J, Heinamaki K, Iwai H. FEBS Lett. 2009 May 6;583(9):1451-6. doi: 10.1016/j.febslet.2009.03.058. Epub 2009 Apr 1. 10.1016/j.febslet.2009.03.058 PubMed 19344715