pICH-chl-roGFP2-GPXC71S
(Plasmid
#191703)
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PurposeTi plasmid pICH86988 harbouring roGFP2-GPXC71S -a plastid-targeted control roGFP2 fusion not responsive to peroxides used alongside plasmids 191699 and 191701
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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 | 191703 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepICH86988
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Backbone manufacturerGolden Gate Addgene number #48076
- Backbone size w/o insert (bp) 9078
- Total vector size (bp) 9983
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Modifications to backboneAdded in during cloning: The level 0 chloroplast transiit peptide coding sequence from pICH78133 (Addgene #50292).
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Vector typePlant Expression ; Binary Agrobacterium Ti plasmid
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Selectable markerskanamycin
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
Gene/Insert
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Gene/Insert namechl-redox(ro)GFP2-GPXC71S
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SpeciesSynthetic
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Insert Size (bp)1497
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MutationPeroxidatic Cysteine 71 replaced with Serine
- Promoter CaMV 35S
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site Bsa1 (destroyed during cloning)
- 3′ cloning site Bsa1 (destroyed during cloning)
- 5′ sequencing primer unknown
- 3′ sequencing primer unknown (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 GPXC71S version was synthesised de novo. Please visit https://doi.org/10.1101/2024.01.18.576236 for bioRxiv preprint.
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:
pICH-chl-roGFP2-GPXC71S was a gift from Philip Mullineaux (Addgene plasmid # 191703 ; http://n2t.net/addgene:191703 ; RRID:Addgene_191703) -
For your References section:
A novel glutathione peroxidase-based biosensor disentangles differential subcellular accumulation of H2O2 and lipid hydroperoxides. Exposito-Rodriguez M, Reeder B, Brooke GN, Hough MA, Laissue PP, Mullineaux PM. bioRxiv 2024.01.18.576236 10.1101/2024.01.18.576236