Skip to main content
This website uses cookies to ensure you get the best experience. By continuing to use this site, you agree to the use of cookies.

Please note: Your browser does not support the features used on Addgene's website. You may not be able to create an account or request plasmids through this website until you upgrade your browser. Learn more

Please note: Your browser does not fully support some of the features used on Addgene's website. If you run into any problems registering, depositing, or ordering please contact us at [email protected]. Learn more

Addgene

pGAL4-CREB S133A
(Plasmid #15222)

Ordering

Item Catalog # Description Quantity Price (USD)
Plasmid 15222 Standard format: Plasmid sent in bacteria as agar stab 1 $85

This material is available to academics and nonprofits only.

Backbone

  • Vector backbone
    pM
  • Backbone manufacturer
    Clontech
  • Backbone size w/o insert (bp) 3500
  • Vector type
    Mammalian Expression

Growth in Bacteria

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

Gene/Insert

  • Gene/Insert name
    CREB S133A
  • Alt name
    CREB
  • Species
    R. norvegicus (rat)
  • Insert Size (bp)
    1000
  • Mutation
    Serine 133 mutated to Alanine
  • Entrez Gene
    Creb1 (a.k.a. Creb)
  • Tag / Fusion Protein
    • Gal4 (N terminal on backbone)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site XhoI/SalI (destroyed during cloning)
  • 3′ cloning site XbaI (not destroyed)
  • 5′ sequencing primer Gal4-N-term primer
  • (Common Sequencing Primers)

Resource Information

  • A portion of this plasmid was derived from a plasmid made by
    CREB kindly provided by Richard A. Maurer
  • Article Citing this Plasmid

Terms and Licenses

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

Depositor Comments

Wild-type CREB S133A fused to the DNA binding domain of Gal4. The plasmids were generated by cloning the CREB S133A as an XhoI/XbaI fragment into the SalI/XbaI sites of pM.

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:

    pGAL4-CREB S133A was a gift from Ugo Moens (Addgene plasmid # 15222 ; http://n2t.net/addgene:15222 ; RRID:Addgene_15222)
  • For your References section:

    The cAMP signalling pathway activates CREB through PKA, p38 and MSK1 in NIH 3T3 cells. Delghandi MP, Johannessen M, Moens U. Cell Signal. 2005 Nov . 17(11):1343-51. 10.1016/j.cellsig.2005.02.003 PubMed 16125054