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PurposeExpression of tdTomato under the control of the TRE-promoter
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 50798 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepUAS-luc2
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Backbone manufacturerLiqun Luo
- Backbone size w/o insert (bp) 2562
- Total vector size (bp) 4356
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Vector typeMutli-species
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 nameTREtight driven tdTomato fluorescent protein
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Alt nameTRE-tdTomato
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Alt nameTRE-tdT
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Insert Size (bp)1794
- Promoter TREtight
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SphI (not destroyed)
- 3′ cloning site XbaI (not destroyed)
- 5′ sequencing primer TGCAGGTGCCAGAACATTTCTC
- 3′ sequencing primer CTGCATTCTAGTTGTGGTTTGTCC (Common Sequencing Primers)
Resource Information
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Article 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.
Depositor Comments
Tang J.C. et al. (2013). A nanobody-based system using fluorescent proteins as scaffolds for cell-specific gene manipulation. Cell. 2013 Aug 15;154(4):928-39.
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:
pTRE-tdTomato was a gift from Connie Cepko (Addgene plasmid # 50798 ; http://n2t.net/addgene:50798 ; RRID:Addgene_50798) -
For your References section:
A nanobody-based system using fluorescent proteins as scaffolds for cell-specific gene manipulation. Tang JC, Szikra T, Kozorovitskiy Y, Teixiera M, Sabatini BL, Roska B, Cepko CL. Cell. 2013 Aug 15;154(4):928-39. doi: 10.1016/j.cell.2013.07.021. 10.1016/j.cell.2013.07.021 PubMed 23953120