pCOCK CMVwt
(Plasmid
#46559)
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PurposeMammalian expression plasmid with EGFP expressed from CMV wild-type promoter.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 46559 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepEF5-FRT-V5-DEST
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Backbone manufacturerLife Technologies
- Backbone size w/o insert (bp) 7528
- Total vector size (bp) 6184
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Modifications to backbone1. EF1alpha promoter removed (so attR Gateway sites can be used to clone in synthetic promoters) 2. IVS-EGFP cassette inserted between attR Gateway cassette and BGH polyA 3. Synthetic promoters flanked by attL in pDONR221 (Life Technologies) vectors were used to recombine promoters into the vector resulting from modifications 1 and 2 above.
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Vector typeMammalian Expression, Synthetic Biology
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Selectable markersHygromycin ; No ATG until recombines into FRT site in target cell genome
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)XL1 Blue
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameCMV wt promoter
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SpeciesCytomegalovirus viral promoter
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Insert Size (bp)589
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MutationOur version has a G at base 724 (reference has C)
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GenBank ID# K03104.1 (bases 156 to 744)
- Promoter CMV
Cloning Information
- Cloning method Gateway Cloning
- 5′ sequencing primer CMV 5' end primer
- 3′ sequencing primer T3 (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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:
pCOCK CMVwt was a gift from Clifford Wang (Addgene plasmid # 46559 ; http://n2t.net/addgene:46559 ; RRID:Addgene_46559) -
For your References section:
Modulating ectopic gene expression levels by using retroviral vectors equipped with synthetic promoters. Ferreira JP, Peacock RW, Lawhorn IE, Wang CL. Syst Synth Biol. 2011 Dec;5(3-4):131-8. doi: 10.1007/s11693-011-9089-0. Epub 2011 Nov 20. 10.1007/s11693-011-9089-0 PubMed 23205156