UbSYRAP_pDONR201
(Plasmid
#249816)
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PurposeEncodes UbSYRAP, a SYRAP split version (UBQ-RAP2.12-GAL4STE12), Gateway compatible as Donor plasmid
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Depositing Lab
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Publication
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Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 249816 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $89 | |
Backbone
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Vector backbonepDONR201
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Backbone manufacturerThermo Fisher scientific
- Backbone size w/o insert (bp) 2040
- Total vector size (bp) 4253
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Vector typeYeast Expression, Plant Expression, Synthetic Biology
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 numberUnknown
Gene/Insert
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Gene/Insert nameUBQ-RAP2.12-GAL4STE
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Alt nameSYRAP
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SpeciesS. cerevisiae (budding yeast), A. thaliana (mustard weed)
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Insert Size (bp)1992
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GenBank IDNP_175794.1
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Entrez GeneRAP2.12 (a.k.a. AT1G53910, T18A20.14, T18A20_14, related to AP2 12)
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Tags
/ Fusion Proteins
- GAL4-STE12 (C terminal on insert)
- UBQ (N terminal on insert)
Cloning Information
- Cloning method Gateway Cloning
- 5′ sequencing primer CCTGGCAGTTCCCTACTCTCGCGTT
- 3′ sequencing primer ATGTAACATCAGAGATTTTGAGACA
- (Common Sequencing Primers)
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
Please visit https://doi.org/10.1101/2025.09.01.673502 for the 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:
UbSYRAP_pDONR201 was a gift from Francesco Licausi (Addgene plasmid # 249816 ; http://n2t.net/addgene:249816 ; RRID:Addgene_249816) -
For your References section:
A synthetic ERFVII-dependent circuit in yeast sheds light on the regulation of early hypoxic responses of plants. Lavilla-Puerta M, He Y, Piccinini L, Di Paco L, Papachristodoulou A, Licausi F, Giuntoli B. bioRxiv 2025.09.01.673502 10.1101/2025.09.01.673502