pIA028
(Plasmid
#200419)
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Purpose(Empty Backbone) thrC::(PAmCherry1 erm2),for PAmCherry1 fusions.PALM integration vector for B. subtilis. Includes PAmCherry1 photoactivatable FP with multi cloning sites (MCS) for fast and interchangeable cloning
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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 | 200419 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepDG1664
- Backbone size (bp) 6102
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Vector typeBacterial Expression
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Selectable markersErythromycin
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Tag
/ Fusion Protein
- PAmCherry1 (C terminal on backbone)
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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Growth instructionsE. coli: 37°C and selection ampicillin 100 μg/mL B. subtilis: 30°C and selection erythromycin 0.5 μg/mL
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Copy numberLow Copy
Cloning Information
- Cloning method Gibson Cloning
Resource Information
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Supplemental Documents
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 PAmCherry1 sequence was amplified from pEYY133 using primers oIA008 and oIA048, then cloned into pIA023 digested with BamHI and SphI, resulting in plasmid pIA028.
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:
pIA028 was a gift from Rut Carballido-López (Addgene plasmid # 200419 ; http://n2t.net/addgene:200419 ; RRID:Addgene_200419) -
For your References section:
New PALM-compatible integration vectors for use in the Gram-positive model bacterium Bacillus subtilis. Altinoglu I, Carballido-Lopez R. bioRxiv 2023 10.1101/2023.03.16.532899