pDA2ScIfm
(Plasmid
#193786)
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PurposeExpresses frame-shifted CI under the control of PLTATAA synthetic promoter, carries a synthetic fragment with additional restriction sites, ColE1 origin of replication, Ampicillin selection
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 193786 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepZ
- Backbone size w/o insert (bp) 2861
- Total vector size (bp) 3574
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Vector typeBacterial Expression, Synthetic Biology
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 nameFrame-shifted CI
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SpeciesMutated Lambda CI
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Insert Size (bp)713
- Promoter PLTATAA synthetic promoter carrying binding sites for LacI and TetR
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site KpnI (unknown if destroyed)
- 3′ cloning site XbaI (unknown if destroyed)
- 5′ sequencing primer AAAGAAACCATTA ACACAAGAGCA
- 3′ sequencing primer TCAGCCAAACGTC TCTTCAG (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.
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:
pDA2ScIfm was a gift from Sangram Bagh (Addgene plasmid # 193786 ; http://n2t.net/addgene:193786 ; RRID:Addgene_193786) -
For your References section:
A frame-shifted gene, which rescued its function by non-natural start codons and its application in constructing synthetic gene circuits. Sarkar K, Mukhopadhyay S, Bonnerjee D, Srivastava R, Bagh S. J Biol Eng. 2019 Mar 1;13:20. doi: 10.1186/s13036-019-0151-x. eCollection 2019. 10.1186/s13036-019-0151-x PubMed 30867677