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Depositing Lab
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Publication
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Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 15221 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepM
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 3500
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Vector typeMammalian Expression
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameCREB
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SpeciesR. norvegicus (rat)
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Insert Size (bp)1000
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Entrez GeneCreb1 (a.k.a. Creb)
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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
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A portion of this plasmid was derived from a plasmid made byCREB kindly provided by Richard A. Maurer
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Article Citing this Plasmid
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
Wild-type CREB fused to the DNA binding domain of Gal4. The plasmids were generated by cloning the cDNA of CREB as an XhoI/XbaI fragment into the SalI/XbaI sites of pM.
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.
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For your Materials & Methods section:
pGAL4-CREB was a gift from Ugo Moens (Addgene plasmid # 15221 ; http://n2t.net/addgene:15221 ; RRID:Addgene_15221) -
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