pQE30-TEV-pro-conA
(Plasmid
#159527)
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PurposeExpresses pro-concanavalin A, a lectin from Canavalia ensiformis, in E. coli. Includes N-terminal TEV recognition site. Native N-terminal sequence is reconstituted upon TEV cleavage.
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 159527 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepQE30
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Backbone manufacturerQIAGEN
- Backbone size w/o insert (bp) 3434
- Total vector size (bp) 4247
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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 nameCanavalia ensiformis pro-concanavalin A
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Alt namepro-conA
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SpeciesSynthetic
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Insert Size (bp)813
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GenBank IDAF308777
- Promoter T5
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Tags
/ Fusion Proteins
- Six-Histidine tag (N terminal on backbone)
- tobacco etch virus (TEV) protease recognition site (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site SalI (not destroyed)
- 5′ sequencing primer CCCGAAAAGTGCCACCTG
- 3′ sequencing primer GTTCTGAGGTCATTACTGG (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
Please visit https://www.biorxiv.org/content/10.1101/2020.10.28.360099v1 for bioRxiv preprint.
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:
pQE30-TEV-pro-conA was a gift from Joshua Mylne (Addgene plasmid # 159527 ; http://n2t.net/addgene:159527 ; RRID:Addgene_159527) -
For your References section:
Structural basis for a natural circular permutation in proteins. Nonis SG, Haywood J, Schmidberger JW, Bond CS, Mylne JS. bioRxiv. 2020. 10.1101/2020.10.28.360099