pCAG-mCherry-FKBP-GEF(ARHGEF1)
(Plasmid
#85152)
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Purposeacute activation of Rho through rapamycin-induced translocation to membrane-localized FRB
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 85152 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCAGEN
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Backbone manufacturerAddgene plasmid #11160
- Backbone size w/o insert (bp) 4798
- Total vector size (bp) 6661
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Vector typeMammalian 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 nameFusion of mCherry, FKBP, and the DH-domain of ARHGEF1 (amino acids 380-630)
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SpeciesH. sapiens (human)
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Insert Size (bp)1875
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Entrez GeneARHGEF1 (a.k.a. GEF1, IMD62, LBCL2, LSC, P115-RHOGEF, SUB1.5)
- Promoter CAG
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Tag
/ Fusion Protein
- mCherry-FKBP (N terminal on insert)
Cloning Information
- Cloning method Gibson Cloning
- 5′ sequencing primer GTTATTGTGCTGTCTCATC
- 3′ sequencing primer ACACCAGCCACCACCTTC (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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 synthetic activation of Rho through Rapamycin-induced translocation of a RhoGEF domain to the plasma membrane. Requires co-expression with plasma membrane-localized FRB, e.g. Lyn11-targeted FRB, Addgene plasmid #20147
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:
pCAG-mCherry-FKBP-GEF(ARHGEF1) was a gift from Tobias Meyer (Addgene plasmid # 85152 ; http://n2t.net/addgene:85152 ; RRID:Addgene_85152) -
For your References section:
Engulfed cadherin fingers are polarized junctional structures between collectively migrating endothelial cells. Hayer A, Shao L, Chung M, Joubert LM, Yang HW, Tsai FC, Bisaria A, Betzig E, Meyer T. Nat Cell Biol. 2016 Dec;18(12):1311-1323. doi: 10.1038/ncb3438. Epub 2016 Nov 14. 10.1038/ncb3438 PubMed 27842057