BioBrick pET-24a(+)
(Plasmid
#117802)
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Purpose(Empty Backbone) BioBrick pET vector for protein overexpression in E. coli
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 117802 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET-24a(+)
- Backbone size (bp) 5018
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Modifications to backboneModifications to backbone: polylinker changed to contain the four standard BioBrick restriction sites EcoRI, XbaI, SpeI and PstI; the remaining sequence lacks these 4 BioBrick sites. The 5’-to-3’ annotation of the insert is BglII, BioBrick prefix (EcoRI, NotI, XbaI), T7 RNA polymerase promoter, lac operator, epsilon translation enhancer, Shine-Dalgarno sequence, NdeI/ATG start codon, minigene (including XhoI site and VSV in vitro transcription terminator), stop codon, 119-nucleotide Tphi transcription terminator, BioBrick suffix (SpeI, NotI, PstI) and BspEI (not unique).
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Vector typeEscherichia coli
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberHigh Copy
Cloning Information
- Cloning method Restriction Enzyme
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:
BioBrick pET-24a(+) was a gift from Anthony Forster (Addgene plasmid # 117802 ; http://n2t.net/addgene:117802 ; RRID:Addgene_117802) -
For your References section:
Engineering multigene expression in vitro and in vivo with small terminators for T7 RNA polymerase. Du L, Gao R, Forster AC. Biotechnol Bioeng. 2009 Dec 15;104(6):1189-96. doi: 10.1002/bit.22491. 10.1002/bit.22491 PubMed 19650080