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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 13568 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepRSET-B
- Backbone size w/o insert (bp) 2897
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Vector typeBacterial 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 numberHigh Copy
Gene/Insert
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Gene/Insert nameFLIPglu F16A Y12S-ECFP-D13R, 6aa linker
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Alt namemglB with ECFP inserted
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Alt namePeriplasmic glucose binding
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SpeciesE. coli
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Insert Size (bp)2400
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MutationF16A, ECFP insert in mglB
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Tag
/ Fusion Protein
- Citrine (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer na (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byCitrine is from Roger Tsien, UCSD.
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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.
Depositor Comments
For more information, see
http://carnegiedpb.stanford.edu/research/frommer/nanosensors/index.html
Citrine is modified version of EYFP.
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:
pRSET FLII12Pglu-700uDelta6 was a gift from Wolf Frommer (Addgene plasmid # 13568 ; http://n2t.net/addgene:13568 ; RRID:Addgene_13568) -
For your References section:
GLUT1 and GLUT9 as major contributors to glucose influx in HepG2 cells identified by a high sensitivity intramolecular FRET glucose sensor. Takanaga H, Chaudhuri B, Frommer WB. Biochim Biophys Acta. 2008 Apr . 1778(4):1091-9. 10.1016/j.bbamem.2007.11.015 PubMed 18177733