pATCH1
(Plasmid
#39274)
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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 | 39274 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepKSS
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Backbone manufacturerPeter Kast Lab
- Backbone size w/o insert (bp) 2443
- Total vector size (bp) 2863
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)XL1 Blue
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameUpdated MCS for pET vectors with enhanced stop codons
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Insert Size (bp)420
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GenBank IDAF013597
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site XhoI (not destroyed)
- 3′ cloning site DraIII (not destroyed)
- 5′ sequencing primer T3 (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
The pET vectors have a leaky UGA stop codon. Plasmid pATCH1 provides a replacement sequence for the inefficient stop signal and can be used to repair both pET vectors and existing pET-based expression constructs.
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:
pATCH1 was a gift from Peter Kast (Addgene plasmid # 39274 ; http://n2t.net/addgene:39274 ; RRID:Addgene_39274) -
For your References section:
UGA read-through artifacts--when popular gene expression systems need a pATCH. MacBeath G, Kast P. Biotechniques. 1998 May;24(5):789-94. 10.2144/98245st02 PubMed 9591128