pSub-MBP-GFP(2M-IKQE)
(Plasmid
#185757)
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PurposeBacterial expression of MBP-GFP(2M IKQE)
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 185757 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepMAL-C2
- Backbone size w/o insert (bp) 5463
- Total vector size (bp) 7422
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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 numberLow Copy
Gene/Insert
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Gene/Insert nameGFP(2M-IKQE)
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Alt namesfGFP with internal LACE tag (IKQE)
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SpeciesSynthetic
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Insert Size (bp)1959
- Promoter tac
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Tag
/ Fusion Protein
- MBP (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site XhoI (not destroyed)
- 5′ sequencing primer MBP-F
- 3′ sequencing primer pBAD Reverse (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
GFP-I for use as a ubiquitination substrate in lysine acylation using conjugating enzymes.
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:
pSub-MBP-GFP(2M-IKQE) was a gift from Jeffrey Bode (Addgene plasmid # 185757 ; http://n2t.net/addgene:185757 ; RRID:Addgene_185757) -
For your References section:
Site-Specific Protein Ubiquitylation Using an Engineered, Chimeric E1 Activating Enzyme and E2 SUMO Conjugating Enzyme Ubc9. Akimoto G, Fernandes AP, Bode JW. ACS Cent Sci. 2022 Feb 23;8(2):275-281. doi: 10.1021/acscentsci.1c01490. Epub 2022 Feb 9. 10.1021/acscentsci.1c01490 PubMed 35237717