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Purpose(Empty Backbone) To facilitate restriction cloning of an RNA of interest with a TGT recognition element in the 3' region
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 138209 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA3.1(+)
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Backbone manufacturerInvitrogen
- Backbone size (bp) 5500
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Vector typeMammalian Expression ; T7 Transcription
- Promoter CMV Promoter, T7 Promoter
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Tag
/ Fusion Protein
- TAG sequence
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 numberUnknown
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer CMV Promoter (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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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
An RNA of interest can be cloned into this vector in order to append a 25-nucleotide TGT recognition element to its 3' end. The TGT recognition element, or TAG, has short spacer arms at either side.
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:
pcDNA3.1-(empty)-TAG was a gift from Neal Devaraj (Addgene plasmid # 138209 ; http://n2t.net/addgene:138209 ; RRID:Addgene_138209) -
For your References section:
Enzymatic covalent labeling of RNA with RNA transglycosylation at guanosine (RNA-TAG). Busby KN, Devaraj NK. Methods Enzymol. 2020;641:373-399. doi: 10.1016/bs.mie.2020.03.009. Epub 2020 Apr 20. 10.1016/bs.mie.2020.03.009 PubMed 32713531