hPRL1_1-169_C104D
(Plasmid
#209793)
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PurposeBacterial expression of human PRL-1 C104D mutant without farnesylation motif
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 209793 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET15b
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Backbone manufacturerNovagen
- Backbone size w/o insert (bp) 5708
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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 namePRL-1
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SpeciesH. sapiens (human)
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Mutationaa 1-169 only; C101D
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Entrez GenePTP4A1 (a.k.a. HH72, PRL-1, PRL1, PTP(CAAX1), PTPCAAX1)
- Promoter T7
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Tag
/ Fusion Protein
- 6xHis (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NdeI (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer T7 Fwd
- 3′ sequencing primer T7 Rev (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made bycodon-optimized gene synthesis
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:
hPRL1_1-169_C104D was a gift from Kalle Gehring (Addgene plasmid # 209793 ; http://n2t.net/addgene:209793 ; RRID:Addgene_209793) -
For your References section:
PRL3 pseudophosphatase activity is necessary and sufficient to promote metastatic growth. Kozlov G, Funato Y, Chen YS, Zhang Z, Illes K, Miki H, Gehring K. J Biol Chem. 2020 Aug 14;295(33):11682-11692. doi: 10.1074/jbc.RA120.014464. Epub 2020 Jun 22. 10.1074/jbc.RA120.014464 PubMed 32571875