pGEX-4T1-Rac1 G15A
(Plasmid
#69355)
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Purposeexpression of nucleotide free Rac1 in bacterial cells
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Depositing Lab
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Publication
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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 | 69355 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepGEX-4T1
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Backbone manufacturerGE
- Backbone size w/o insert (bp) 4900
- Total vector size (bp) 5500
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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 nameRac1
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Alt nameMIG5
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Alt nameTC-25
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Alt namep21-Rac1
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SpeciesH. sapiens (human)
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Insert Size (bp)576
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MutationG15A
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GenBank ID5879
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Entrez GeneRAC1 (a.k.a. MIG5, MRD48, Rac-1, TC-25, p21-Rac1)
- Promoter tac
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Tag
/ Fusion Protein
- GST (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site XhoI (not destroyed)
- 5′ sequencing primer pGEX5
- 3′ sequencing primer pGEX3 (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byKeith Burridge Lab, UNC Chapel Hill
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
Rac1 has a mutation, G15A, which makes it nucleotide free when expressed in bacteria, which can be used GEF pulldowns.
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:
pGEX-4T1-Rac1 G15A was a gift from Rafael Garcia-Mata (Addgene plasmid # 69355 ; http://n2t.net/addgene:69355 ; RRID:Addgene_69355) -
For your References section:
Analysis of activated GAPs and GEFs in cell lysates. Garcia-Mata R, Wennerberg K, Arthur WT, Noren NK, Ellerbroek SM, Burridge K. Methods Enzymol. 2006;406:425-37. 10.1016/S0076-6879(06)06031-9 PubMed 16472675