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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 | 41088 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepEGFP-N1
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Backbone manufacturerclontech
- Backbone size w/o insert (bp) 4733
- Total vector size (bp) 5669
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Modifications to backbonePCR-amplified insert was blunt-end ligated into pPCR-Script AMP vector, removed by digestion with HindIII and KpnI, and ligated into pEGFP-N1
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 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 nameReceptor for activated C kinase
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Alt nameRACK1
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Alt nameGNB2L1
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SpeciesH. sapiens (human)
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Insert Size (bp)954
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GenBank IDNM_006098.4
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Entrez GeneRACK1 (a.k.a. GNB2L1, Gnb2-rs1, H12.3, HLC-7, PIG21)
- Promoter CMV
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Tag
/ Fusion Protein
- GFP (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site KpnI (not destroyed)
- 5′ sequencing primer EGFP-N
- 3′ sequencing primer EGFP_C_primer (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made bypcDNA3.1 RACK1 was recieved from T.E. O'Toole at Scripps Research Institute [email protected] then cloned into N1-pEGFP
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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.
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:
pEGFP-N1-RACK1 was a gift from Anna Huttenlocher (Addgene plasmid # 41088 ; http://n2t.net/addgene:41088 ; RRID:Addgene_41088) -
For your References section:
RACK1 regulates integrin-mediated adhesion, protrusion, and chemotactic cell migration via its Src-binding site. Cox EA, Bennin D, Doan AT, O'Toole T, Huttenlocher A. Mol Biol Cell. 2003 Feb;14(2):658-69. 10.1091/mbc.e02-03-0142 PubMed 12589061