pMPRA3-CMV-Clover
(Plasmid
#53540)
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PurposeFluorescent reporter control for pMPRA3
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 53540 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepMPRA3
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Backbone manufacturerBroad Institute
- Total vector size (bp) 5597
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Vector typeMammalian Expression
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Selectable markersTruncated H2Kk cell surface marker
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 numberHigh Copy
Gene/Insert
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Gene/Insert nameClover GFP
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SpeciesSynthetic; Aequorea victoria
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Insert Size (bp)717
- Promoter CMV IE
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SfiI (not destroyed)
- 3′ cloning site SfiI (not destroyed)
- 5′ sequencing primer T7 (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byThe CMV-Clover cassette is based on Addgene Plasmid 40259 (pcDNA3-Clover) from the Michael Lin laboratory, but the physical DNA used to construct pMPRA-CMV-clover was synthesized de novo by Genscript Inc.
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
Addgene sequencing detected an IS1 transposable element
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:
pMPRA3-CMV-Clover was a gift from Tarjei Mikkelsen (Addgene plasmid # 53540 ; http://n2t.net/addgene:53540 ; RRID:Addgene_53540) -
For your References section:
Massively parallel reporter assays in cultured Mammalian cells. Melnikov A, Zhang X, Rogov P, Wang L, Mikkelsen TS. J Vis Exp. 2014 Aug 17;(90). doi: 10.3791/51719. 10.3791/51719 PubMed 25177895