pYS7
(Plasmid
#69208)
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PurposeGateway Entry clone for synthetic TetO2-CYC1TATA promoter
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Depositing Lab
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Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 69208 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $89 | |
Backbone
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Vector backbonepDONR221P5-P2
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Backbone manufacturerInvitrogen (Life Technologies)
- Backbone size w/o insert (bp) 2551
- Total vector size (bp) 2804
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Vector typeSynthetic Biology ; Gateway Entry clone
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 nameSynthetic TetO2 + S.cerevisiae CYC1 minimal promoter (TATA)
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SpeciesS. cerevisiae (budding yeast), Synthetic
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Insert Size (bp)253
Cloning Information
- Cloning method Gateway Cloning
- 5′ sequencing primer M13 forward
- 3′ sequencing primer M13 reverse
- (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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A portion of this plasmid was derived from a plasmid made byTetO7-CYC1TATA promoter was amplified by PCR using pCM171 (obtained from EUROSCARF) as a template and cloned by Gateway BP reaction.
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:
pYS7 was a gift from Yasushi Saka (Addgene plasmid # 69208) -
For your References section:
Gateway vectors for efficient artificial gene assembly in vitro and expression in yeast Saccharomyces cerevisiae. Giuraniuc CV, MacPherson M, Saka Y. PLoS One. 2013 May 10;8(5):e64419. doi: 10.1371/journal.pone.0064419. Print 2013. PONE-D-13-07010 [pii] PubMed 23675537