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PurposeFor use in light-induced protein inactivation through the interaction with CRY2
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 58366 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepmCerulean-C1
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 4742
- Total vector size (bp) 5720
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Vector typeMammalian Expression
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 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 1
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Gene/Insert nameCIB1[1-147]
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Alt namecryptochrome-interacting basic-helix-loop-helix 1
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Alt nameT4L20.110
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Alt nameT4L20_110
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SpeciesA. thaliana (mustard weed)
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Insert Size (bp)513
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GenBank ID829604
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Entrez GeneCIB1 (a.k.a. AT4G34530, T4L20.110, T4L20_110, cryptochrome-interacting basic-helix-loop-helix 1)
- Promoter CMV
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Tag
/ Fusion Protein
- mCerulean (C terminal on insert)
Cloning Information for Gene/Insert 1
- Cloning method Restriction Enzyme
- 5′ cloning site NheI (not destroyed)
- 3′ cloning site AgeI (not destroyed)
- 5′ sequencing primer CMV Forward (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert nameCamk2a[315-478]
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Alt namecalcium/calmodulin-dependent protein kinase II alpha
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Alt namePKCCD
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Alt namePK2CDD
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SpeciesR. norvegicus (rat)
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Insert Size (bp)498
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GenBank ID25400
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Entrez GeneCamk2a (a.k.a. PK2CDD, PKCCD)
- Promoter CMV
Cloning Information for Gene/Insert 2
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer n/a
- 3′ sequencing primer SV40pA-R (Common Sequencing Primers)
Resource Information
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Articles 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:
pCMV-CIB1-mCerulean-MP was a gift from Won Do Heo (Addgene plasmid # 58366 ; http://n2t.net/addgene:58366 ; RRID:Addgene_58366) -
For your References section:
Reversible protein inactivation by optogenetic trapping in cells. Lee S, Park H, Kyung T, Kim NY, Kim S, Kim J, Heo WD. Nat Methods. 2014 Jun;11(6):633-6. doi: 10.1038/nmeth.2940. Epub 2014 May 4. 10.1038/nmeth.2940 PubMed 24793453