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Addgene

pET-3c-rhVTN_FL
(Plasmid #30223)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 30223 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    pET-3c
  • Backbone manufacturer
    Novagen
  • Backbone size w/o insert (bp) 4607
  • Vector type
    Bacterial Expression

Growth in Bacteria

  • Bacterial Resistance(s)
    Ampicillin, 100 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Growth instructions
    DH5a in LB media
  • Copy number
    Low Copy

Gene/Insert

  • Gene/Insert name
    rhVitronectin without deletions
  • Alt name
    VTN-FL
  • Alt name
    rhVTN-FL
  • Alt name
    VTN
  • Species
    H. sapiens (human)
  • Insert Size (bp)
    1380
  • Mutation
    No deletions
  • Entrez Gene
    VTN (a.k.a. V75, VN, VNT)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site BamHI (not destroyed)
  • 3′ cloning site NdeI (not destroyed)
  • 5′ sequencing primer T7
  • 3′ sequencing primer T7
  • (Common Sequencing Primers)

Terms and Licenses

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

Depositor Comments

Note that the first 19 amino acids are the signal peptide for VTN, which is cleaved off on the mature protein during normally protein synthesis in mammalian cells. That means wild type mature VTN starts from aa20. None of the four constructs from this paper have amino acids 1-19.

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:

    pET-3c-rhVTN_FL was a gift from James Thomson (Addgene plasmid # 30223 ; http://n2t.net/addgene:30223 ; RRID:Addgene_30223)
  • For your References section:

    Chemically defined conditions for human iPSC derivation and culture. Chen G, Gulbranson DR, Hou Z, Bolin JM, Ruotti V, Probasco MD, Smuga-Otto K, Howden SE, Diol NR, Propson NE, Wagner R, Lee GO, Antosiewicz-Bourget J, Teng JM, Thomson JA. Nat Methods. 2011 Apr 10. ():. 10.1038/nmeth.1593 PubMed 21478862