pET21-Streptavidin-K121R
(Plasmid
#89880)
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PurposeStreptavidin that has unimpaired biotin binding after dye labeling
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 89880 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET21
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Backbone manufacturerNovagen
- Backbone size w/o insert (bp) 5400
- Total vector size (bp) 5802
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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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Growth instructionsDH5alpha for propagation of the plasmid. Bl21[DE3] or similar required for protein expression.
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Copy numberLow Copy
Gene/Insert
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Gene/Insert nameStreptavidin-K121R-Glutamate_Tag
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Alt nameSAe-K121R
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SpeciesE. coli
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Insert Size (bp)402
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MutationK121R
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Tag
/ Fusion Protein
- 6 glutamate tag (C terminal on insert)
Cloning Information
- Cloning method Unknown
- 5′ sequencing primer T7F
- 3′ sequencing primer T7R (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
The residue numbering is based 1986 paper from Charles Cantor: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC339579 (see Figure 3)
In the original sequence, there is a signal peptide and N-terminal sequence that are proteolytically processed. Thus, the most common version is Core Streptavidin, which starts at residue 13 and ends at residue 139, as shown here: http://www.jbc.org/content/270/47/28204.long (see Figure 1)
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:
pET21-Streptavidin-K121R was a gift from Mark Howarth (Addgene plasmid # 89880 ; http://n2t.net/addgene:89880 ; RRID:Addgene_89880) -
For your References section:
Amine Landscaping to Maximize Protein-Dye Fluorescence and Ultrastable Protein-Ligand Interaction. Jacobsen MT, Fairhead M, Fogelstrand P, Howarth M. Cell Chem Biol. 2017 Jul 17. pii: S2451-9456(17)30229-5. doi: 10.1016/j.chembiol.2017.06.015. 10.1016/j.chembiol.2017.06.015 PubMed 28757182