pcDNAI-GAL4-CREB-S142A
(Plasmid
#46771)
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PurposeExpression of GAL4 fusion to CREB-S142A
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 46771 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNAI-AMP
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Backbone manufacturerInvitrogen
- Backbone size w/o insert (bp) 4767
- Total vector size (bp) 6206
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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 numberLow Copy
Gene/Insert
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Gene/Insert nameGAL4(1-147)-CREB-S142A
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SpeciesR. norvegicus (rat), S. cerevisiae (budding yeast)
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Insert Size (bp)1500
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MutationChanged CREB serine 142 to Alanine
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GenBank IDNM_001184062.1 NM_134443.1
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Entrez GeneCreb1 (a.k.a. Creb)
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Entrez GeneGAL4 (a.k.a. YPL248C, GAL81)
- Promoter CMV
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Tag
/ Fusion Protein
- GAL4 (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site XbaI (not destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer SP6 (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byThe rat CREB coding sequence was obtained by PCR from mRNA. The GAL4(1-147) coding sequence was obtained from PG424 (Sadowski & Ptashne, Nucleic Acids Res. 17:7539, 1989) which was provided by Dr. Ptashne.
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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.
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:
pcDNAI-GAL4-CREB-S142A was a gift from Richard Maurer (Addgene plasmid # 46771 ; http://n2t.net/addgene:46771 ; RRID:Addgene_46771) -
For your References section:
Differential activation of CREB by Ca2+/calmodulin-dependent protein kinases type II and type IV involves phosphorylation of a site that negatively regulates activity. Sun P, Enslen H, Myung PS, Maurer RA. Genes Dev. 1994 Nov 1;8(21):2527-39. 10.1101/gad.8.21.2527 PubMed 7958915