pcDNA6 MCV LTco S220A
(Plasmid
#112193)
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PurposeExpression of MCPyV LT mutant (Ser 220 to Ala)
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 112193 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA6.V5.HisB
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Backbone manufacturerInvirtogen
- Backbone size w/o insert (bp) 4985
- Total vector size (bp) 7549
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Modifications to backbonepcDNA6.V5.HisB vector was modified with NheI and PmeI restriction digestion enzymes to cut out MCS, V5 and His tag sites. New multiple cloning sites using annealed primer pair were ligated back into the vector. The newly generated cloning site comprises: NheI, KpnI, EcoRV, XhoI and SacII. Codon optimized Large T was cloned between EcoRV and XhoI restriction sites.
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Vector typeMammalian Expression
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Selectable markersBlasticidin
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 nameMCPyV LT codon optimized
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Alt nameMCV LT
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Alt nameMCV large T antigen
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Alt nameMerkel Cell Polyomavirus large T antigen
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SpeciesMerkel cell polyomavirus
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Insert Size (bp)2564
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GenBank IDAEM01097.1
- Promoter CMV
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRV (not destroyed)
- 3′ cloning site XhoI (not destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer BGHr (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.
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:
pcDNA6 MCV LTco S220A was a gift from Patrick Moore (Addgene plasmid # 112193 ; http://n2t.net/addgene:112193 ; RRID:Addgene_112193) -
For your References section:
Protein-mediated viral latency is a novel mechanism for Merkel cell polyomavirus persistence. Kwun HJ, Chang Y, Moore PS. Proc Natl Acad Sci U S A. 2017 May 16;114(20):E4040-E4047. doi: 10.1073/pnas.1703879114. Epub 2017 May 1. 10.1073/pnas.1703879114 PubMed 28461484