pSG69-KcsA-Kv1.3-deGFP
(Plasmid
#102458)
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PurposeExpresses KcsA-Kv1.3 protein with a C-terminal His tag and a deGFP fluorescent protein with a different ribosome binding site.
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 102458 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepBEST
- Backbone size w/o insert (bp) 2541
- Total vector size (bp) 3804
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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 Temperature30°C
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Growth Strain(s)KL740
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Copy numberHigh Copy
Gene/Insert 1
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Gene/Insert nameKcsA-Kv1.3
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Alt nameKcsA
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Alt nameKv1.3
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SpeciesChimera
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Insert Size (bp)495
- Promoter OR2-OR1-Pr
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Tag
/ Fusion Protein
- His tag (C terminal on insert)
Cloning Information for Gene/Insert 1
- Cloning method Unknown
- 5′ sequencing primer AAAACCGAATTTTGCTGGGTG
- 3′ sequencing primer AACGCCAGTGAAAAGCTC (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert namedeGFP
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Alt nameGFP
- Promoter OR2-OR1-Pr
Cloning Information for Gene/Insert 2
- Cloning method Unknown
- 5′ sequencing primer TGCTTGACGATAACCGTC
- 3′ sequencing primer ATGATAAAGAACACAGTCATAAGTGC (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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
Please visit https://www.biorxiv.org/content/early/2017/01/30/104455 for bioRxiv preprint.
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:
pSG69-KcsA-Kv1.3-deGFP was a gift from Richard Murray (Addgene plasmid # 102458 ; http://n2t.net/addgene:102458 ; RRID:Addgene_102458) -
For your References section:
Expressing Biologically Active Membrane Proteins in a Cell-Free Transcription-Translation Platform. Guo S, Vaish A, Chen Q, Murray RM. bioRxiv 104455 10.1101/104455