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            Purpose(Empty Backbone) pcDNA3 converted Gateway Destination vector for mammalian expression
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              Depositing Lab
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          Publication
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          Sequence Information
 
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 18672 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $89 | |
Backbone
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            Vector backbonepcDNA3
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              Backbone manufacturerInvitrogen
 - Backbone size (bp) 7694
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              Modifications to backboneGateway cassette was inserted into original vector to create the pEZY3 Gateway Destination vector
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              Vector typeMammalian Expression
 
Growth in Bacteria
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            Bacterial Resistance(s)Chloramphenicol and Ampicillin, 25 & 100 μg/mL
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            Growth Temperature30°C
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            Growth Strain(s)DB3.1
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              Growth instructionsE.coli strain DB3.1, at 30C
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            Copy numberUnknown
 
Gene/Insert
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                Gene/Insert nameNone
 - Promoter CMV
 
Cloning Information
- Cloning method Restriction Enzyme
 - 5′ cloning site EcoRI (destroyed during cloning)
 - 3′ cloning site XhoI (not destroyed)
 - 5′ sequencing primer CMV-F
 - 3′ sequencing primer BGH-rev (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.
 
Depositor Comments
pcDNA3 Gateway-compatible Destination vector. Combine with an Entry clone containing your gene of interest with the Gateway LR reaction to generate a mammalian expression clone.
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:
pEZY3 was a gift from Yu-Zhu Zhang (Addgene plasmid # 18672 ; http://n2t.net/addgene:18672 ; RRID:Addgene_18672) - 
                
For your References section:
An in vitro recombination method to convert restriction- and ligation-independent expression vectors. Guo F, Chiang MY, Wang Y, Zhang YZ. Biotechnol J. 2008 Mar . 3(3):370-7. 10.1002/biot.200700170 PubMed 18064608