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Depositing Lab
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Publication
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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 | 40190 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepSCC3
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Backbone manufacturern/a
- Backbone size w/o insert (bp) 3000
- Total vector size (bp) 3200
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Modifications to backbonenone
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Vector typeBacterial Expression
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 50 μg/mL
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Growth Temperature30°C
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Growth Strain(s)JC4588 lambda+
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Growth instructionsInduce expression by transfer to 37˚C.
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameEcoRI endonuclease & EcoRI methylase
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SpeciesE. coli
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Insert Size (bp)2210
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Mutationchanged Glutamic Acid 111 to Glutamine
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GenBank IDJ01675.1
- Promoter Lambda PL
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (unknown if destroyed)
- 3′ cloning site BglII (not destroyed)
- 5′ sequencing primer NNNNNN
- 3′ sequencing primer NNNNNN (Common Sequencing Primers)
Resource Information
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Articles Citing this Plasmid
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
pSCC3 plasmid derivation is described in King, K. et al. (1989) J.Biol.Chem. 264, 11807-11815.
Please note that this plasmid may require a unique bacterial strain, so make sure to confirm that you can also obtain the appropriate growth strain. Please contact us at [email protected] or contact our distributors if you have any questions.
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:
pEQ111m was a gift from Paul Modrich (Addgene plasmid # 40190 ; http://n2t.net/addgene:40190 ; RRID:Addgene_40190) -
For your References section:
The negative charge of Glu-111 is required to activate the cleavage center of EcoRI endonuclease. Wright DJ, King K, Modrich P. J Biol Chem. 1989 Jul 15;264(20):11816-21. PubMed 2745418
Map uploaded by the depositor.