pET21a - Ec-ClpX D144L
(Plasmid
#111514)
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PurposeExpresses E. coli ClpX with a C-terminal His tag and a mutation from D144 to L144
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 111514 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepET21a
- Backbone size w/o insert (bp) 5443
- Total vector size (bp) 6736
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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 nameClpX
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Alt nameATP-dependent Clp protease ATP-binding subunit clpX
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SpeciesEscherichia coli
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Insert Size (bp)1275
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MutationAspartatic acid 144 to Leucine
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GenBank IDNC_000913.3
- Promoter T7
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Tag
/ Fusion Protein
- His tag (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer T7 Forward (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
Depositor confirms K408E compared to NC_000913.3 has no impact on function.
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:
pET21a - Ec-ClpX D144L was a gift from Judy Lieberman (Addgene plasmid # 111514 ; http://n2t.net/addgene:111514 ; RRID:Addgene_111514) -
For your References section:
Granzyme B Disrupts Central Metabolism and Protein Synthesis in Bacteria to Promote an Immune Cell Death Program. Dotiwala F, Sen Santara S, Binker-Cosen AA, Li B, Chandrasekaran S, Lieberman J. Cell. 2017 Nov 16;171(5):1125-1137.e11. doi: 10.1016/j.cell.2017.10.004. Epub 2017 Oct 26. 10.1016/j.cell.2017.10.004 PubMed 29107333