Gal ts-lux
(Plasmid
#1329)
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Depositing Lab
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Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 1329 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepRS316 Gal1-10 (based on pBluescript)
- Backbone size w/o insert (bp) 4895
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Vector typeYeast Expression
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 numberLow Copy
Gene/Insert
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Gene/Insert namebacterial luciferase-V.h.MAV
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Alt nameVibrio harveyi luciferase in yeast
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SpeciesVibrio harveyi MAV
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Insert Size (bp)2270
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoR1 (not destroyed)
- 3′ cloning site blunt (destroyed during cloning)
- 5′ sequencing primer M13R (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byA.Szalay, University of Alberta
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
Plasmid with selectable Ura marker, maintained in DH5alphaF'
Using PCR, BamH1 and Sac1 sites were created at the end of the luxAB gene (pLx709-fab9) and this wascloned into pRS316 Gal1-10 vector
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:
Gal ts-lux was a gift from Susan Lindquist (Addgene plasmid # 1329 ; http://n2t.net/addgene:1329 ; RRID:Addgene_1329) -
For your References section:
In vivo functions of the Saccharomyces cerevisiae Hsp90 chaperone. Nathan DF, Vos MH, Lindquist S. Proc Natl Acad Sci U S A 1997 Nov 25;94(24):12949-56. 10.1073/pnas.94.24.12949 PubMed 9371781