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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 | 33130 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepRS314
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Backbone manufacturerATCC
- Backbone size w/o insert (bp) 4783
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Modifications to backboneNotI - T7 promoter - TDH3 5'UTR - BamHI - GFP - SalI - TDH3 3' UTR and polyadenylation signal - EcoRI
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Vector typeYeast Expression
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Selectable markersTRP1
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)TG1
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameGFP with TDH3 5' and 3' UTR
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Entrez Genegfp (a.k.a. pCmGFP_001)
- Promoter T7
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site SalI (not destroyed)
- 5′ sequencing primer T7 forward (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
T7 promoter driven GFP with the TDH3 5' and 3' flanking sequences, and the TDH3 polyadenylation signal all cloned into pRS314 using NotI and EcoRI.
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:
pRS314-T7-GFP was a gift from Michael Rosbash (Addgene plasmid # 33130 ; http://n2t.net/addgene:33130 ; RRID:Addgene_33130) -
For your References section:
T7 RNA polymerase-directed transcripts are processed in yeast and link 3' end formation to mRNA nuclear export. Dower K, Rosbash M. RNA. 2002 May;8(5):686-97. 10.1017/S1355838202024068 PubMed 12022234