env8 reverse J1/13
(Plasmid
#99831)
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PurposeGFPuv reporter that places expression of a fluorescent protein reporter (GFPuv) under control of the env8HyCbl riboswitch.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 99831 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepRR5
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Vector typeBacterial Expression
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 nameenv8 reverse J1/13
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MutationJ1/13 sequence is reversed
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Tag
/ Fusion Protein
- GFPuv (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site unknown (unknown if destroyed)
- 3′ cloning site unknown (unknown if destroyed)
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:
env8 reverse J1/13 was a gift from Robert Batey (Addgene plasmid # 99831 ; http://n2t.net/addgene:99831 ; RRID:Addgene_99831) -
For your References section:
Mechanistic Insights into Cofactor-Dependent Coupling of RNA Folding and mRNA Transcription/Translation by a Cobalamin Riboswitch. Polaski JT, Holmstrom ED, Nesbitt DJ, Batey RT. Cell Rep. 2016 May 3;15(5):1100-10. doi: 10.1016/j.celrep.2016.03.087. Epub 2016 Apr 21. 10.1016/j.celrep.2016.03.087 PubMed 27117410