pGEX-SUMO1
(Plasmid
#185637)
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Purposeexpression of GST-tagged SUMO1 in bacterial cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 185637 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepGEX-4T-1
- Backbone size w/o insert (bp) 4968
- Total vector size (bp) 5264
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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 namesmall ubiquitin-like modifier 1
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SpeciesH. sapiens (human)
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Insert Size (bp)296
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Entrez GeneSUMO1 (a.k.a. DAP1, GMP1, OFC10, PIC1, SENP2, SMT3, SMT3C, SMT3H3, UBL1)
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Tag
/ Fusion Protein
- GST (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SalI (unknown if destroyed)
- 3′ cloning site NotI (unknown if destroyed)
- 5′ sequencing primer pGEX Fwd (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
codon optimized for expression in E. coli
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-SUMO1 was a gift from Irina Bezsonova (Addgene plasmid # 185637 ; http://n2t.net/addgene:185637 ; RRID:Addgene_185637) -
For your References section:
The B-box1 domain of PML mediates SUMO E2-E3 complex formation through an atypical interaction with UBC9. Bregnard T, Ahmed A, Semenova IV, Weller SK, Bezsonova I. Biophys Chem. 2022 Aug;287:106827. doi: 10.1016/j.bpc.2022.106827. Epub 2022 May 18. 10.1016/j.bpc.2022.106827 PubMed 35667129