PL-452 N-CyPet
(Plasmid
#19171)
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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 | 19171 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonePL-452
- Backbone size w/o insert (bp) 4823
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Vector typeCre/Lox
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 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 nameCyPet
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Alt nameCyPet-PL-452
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Speciesjellyfish
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Insert Size (bp)717
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site KpnI (not destroyed)
- 3′ cloning site NheI (not destroyed)
- 5′ sequencing primer n/a (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byDr. Patrick Daugherty, UCSB
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:
PL-452 N-CyPet was a gift from Patrik Verstreken (Addgene plasmid # 19171 ; http://n2t.net/addgene:19171 ; RRID:Addgene_19171) -
For your References section:
Recombineering-mediated tagging of Drosophila genomic constructs for in vivo localization and acute protein inactivation. Venken KJ, Kasprowicz J, Kuenen S, Yan J, Hassan BA, Verstreken P. Nucleic Acids Res. 2008 Aug 1. ():. 10.1093/nar/gkn486 PubMed 18676454