pKanCMV-CX4.3-7aa-mClover3
(Plasmid
#74260)
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PurposeMammalian expression of C-terminal fusion of mClover3 to CX43
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 74260 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepKanCMV
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Backbone manufacturerMichael Davidson Lab
- Backbone size w/o insert (bp) 3900
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Vector typeMammalian Expression
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Selectable markersnone
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
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Gene/Insert nameConnexin 43
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Alt nameCX43
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Insert Size (bp)1146
- Promoter CAG
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Tag
/ Fusion Protein
- mClover3 (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (unknown if destroyed)
- 3′ cloning site NotI (unknown if destroyed)
- 5′ sequencing primer pshuttle5
- 3′ sequencing primer pM3 (Common Sequencing Primers)
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
The specific substitutions used in the development of mClover3 relative to its parent Clover are N149Y, G160C, and A206K.
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:
pKanCMV-CX4.3-7aa-mClover3 was a gift from Michael Lin (Addgene plasmid # 74260 ; http://n2t.net/addgene:74260 ; RRID:Addgene_74260) -
For your References section:
Improving brightness and photostability of green and red fluorescent proteins for live cell imaging and FRET reporting. Bajar BT, Wang ES, Lam AJ, Kim BB, Jacobs CL, Howe ES, Davidson MW, Lin MZ, Chu J. Sci Rep. 2016 Feb 16;6:20889. doi: 10.1038/srep20889. 10.1038/srep20889 PubMed 26879144