EC.RNe.TYB1.a1-395.wt
(Plasmid
#17950)
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Depositing Lab
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Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 17950 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepTYB1
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Backbone manufacturerNew England Biolabs
- Backbone size w/o insert (bp) 7280
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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 instructionsBL21(DE3)
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameEscherichia coli RNase E residues 1-395
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SpeciesE. coli
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Insert Size (bp)1185
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Mutationresidues 1-395
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Tag
/ Fusion Protein
- intein-chitin binding domain (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NdeI (not destroyed)
- 3′ cloning site KpnI (not destroyed)
- 5′ sequencing primer T7 (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byDr. Stan Cohen, Stanford
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.
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:
EC.RNe.TYB1.a1-395.wt was a gift from David McKay (Addgene plasmid # 17950 ; http://n2t.net/addgene:17950 ; RRID:Addgene_17950) -
For your References section:
Retention of core catalytic functions by a conserved minimal ribonuclease E peptide that lacks the domain required for tetramer formation. Caruthers JM, Feng Y, McKay DB, Cohen SN. J Biol Chem. 2006 Sep 15. 281(37):27046-51. 10.1074/jbc.M602467200 PubMed 16854990