pHBJT001
(Plasmid
#225152)
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Purpose(Empty Backbone) High copy cloning vector for integration of C-terminal FLAG epitope tag. SmaI restriction site immediately upstream of the FLAG epitope. FLAG epitope in same orientation as lac promoter.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 225152 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepUC19
- Backbone size (bp) 2686
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Vector typeBacterial Expression, Synthetic Biology
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Tag
/ Fusion Protein
- FLAG epitope tag (35 bp) (C terminal on insert)
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 nameNone
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Tag
/ Fusion Protein
- FLAG epitope tag (35 bp) (C terminal on insert)
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
High copy plasmid (pMB1 ori), pUC19 MCS with FLAG epitope integrated, confers ampicillin resistance
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:
pHBJT001 was a gift from Jenny-Lee Thomassin (Addgene plasmid # 225152 ; http://n2t.net/addgene:225152 ; RRID:Addgene_225152) -
For your References section:
Generation of a plasmid series for rapid sub-cloning and use in various Enterobacteriaceae. Braun HG, Kanwal N, Rivera Lopez LF, Thomassin JL. J Biosci Bioeng. 2024 Sep 6:S1389-1723(24)00253-6. doi: 10.1016/j.jbiosc.2024.08.006. 10.1016/j.jbiosc.2024.08.006 PubMed 39244484