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Addgene

pET28a-HisYFP-Sp100
(Plasmid #53141)

Ordering

Item Catalog # Description Quantity Price (USD)
Plasmid 53141 Standard format: Plasmid sent in bacteria as agar stab 1 $85

This material is available to academics and nonprofits only.

Backbone

  • Vector backbone
    pET28a
  • Backbone manufacturer
    Novagen
  • Backbone size w/o insert (bp) 5369
  • Total vector size (bp) 7283
  • Vector type
    Bacterial Expression

Growth in Bacteria

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

Gene/Insert

  • Gene/Insert name
    Sp100A fragment
  • Species
    H. sapiens (human)
  • Insert Size (bp)
    2028
  • Mutation
    fragment (amino acids 71-480); deletion of L75
  • GenBank ID
  • Entrez Gene
    SP100 (a.k.a. lysp100b)
  • Promoter T7
  • Tag / Fusion Protein
    • His-YFP (N terminal on insert)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site EcoRI (not destroyed)
  • 3′ cloning site SalI (not destroyed)
  • 5′ sequencing primer T7
  • 3′ sequencing primer T7-term
  • (Common Sequencing Primers)

Terms and Licenses

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

Depositor Comments

Please note that the plasmid contains some 3'UTR sequence following the CDS that is not found in the full plasmid sequence. This does not have any functional consequence.

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:

    pET28a-HisYFP-Sp100 was a gift from Frauke Melchior (Addgene plasmid # 53141 ; http://n2t.net/addgene:53141 ; RRID:Addgene_53141)
  • For your References section:

    Recombinant reconstitution of sumoylation reactions in vitro. Flotho A, Werner A, Winter T, Frank AS, Ehret H, Melchior F. Methods Mol Biol. 2012;832:93-110. doi: 10.1007/978-1-61779-474-2_5. 10.1007/978-1-61779-474-2_5 PubMed 22350878