pRetro-XT-PAK2-CFP(puro)-L107F
(Plasmid
#81180)
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PurposeRetroviral vector for expression of kinase active PAK2 with a CFP fusion
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Depositing Lab
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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 | 81180 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepRetroX-Tight-Pur
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 6567
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Vector typeRetroviral
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Selectable markersPuromycin
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature30°C
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Growth Strain(s)NEB Stable
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert namep21 (RAC1) activated kinase 2
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Alt namePAK2
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SpeciesH. sapiens (human)
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MutationL107F
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Entrez GenePAK2 (a.k.a. KNO2, PAK65, PAKgamma)
- Promoter P-tight TRE
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Tag
/ Fusion Protein
- CFP (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NotI (unknown if destroyed)
- 3′ cloning site NruI (unknown if destroyed)
- 5′ sequencing primer pBABE 5
- 3′ sequencing primer MSCV-rev (Common Sequencing Primers)
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
There is a coding difference of L106F rather than L107F in the PAK2 insert compared to NP_002568.2.
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:
pRetro-XT-PAK2-CFP(puro)-L107F was a gift from Angeliki Malliri (Addgene plasmid # 81180 ; http://n2t.net/addgene:81180 ; RRID:Addgene_81180) -
For your References section:
Cdk1 phosphorylates the Rac activator Tiam1 to activate centrosomal Pak and promote mitotic spindle formation. Whalley HJ, Porter AP, Diamantopoulou Z, White GR, Castaneda-Saucedo E, Malliri A. Nat Commun. 2015 Jun 16;6:7437. doi: 10.1038/ncomms8437. 10.1038/ncomms8437 PubMed 26078008