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PurposeHR donor to integrate UAS1B8TEF(136)-hrGFP-CYC1t into XPR2 locus
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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 | 84614 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepUC19
- Backbone size w/o insert (bp) 2623
- Total vector size (bp) 8873
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Vector typeYeast Expression, Synthetic Biology
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Selectable markersURA3
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 namehrGFP
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Insert Size (bp)720
- Promoter UAS1B8-TEF(136)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BssHII (not destroyed)
- 3′ cloning site NheI (not destroyed)
- 5′ sequencing primer TEF
- 3′ sequencing primer CYC (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byAddgene material #44380 (UAS1B8-TEF promoter) is used to express hrGFP
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Articles Citing this Plasmid
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:
pHR_XPR2_hrGFP was a gift from Ian Wheeldon (Addgene plasmid # 84614 ; http://n2t.net/addgene:84614 ; RRID:Addgene_84614) -
For your References section:
Standardized markerless gene integration for pathway engineering in Yarrowia lipolytica. Schwartz C, Shabbir-Hussain M, Frogue K, Blenner M, Wheeldon I. ACS Synth Biol. 2016 Dec 19. 10.1021/acssynbio.6b00285 PubMed 27989123