pDrBB2
(Plasmid
#18946)
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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 | 18946 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepHZ-attB
- Backbone size w/o insert (bp) 4622
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Vector typeInsect Expression
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Selectable markersHygromycin
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 namehygromycin gene driven by the copia promoter, phiC31 attB
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Alt namephiC31 bacterial attachment site
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SpeciesEscherichia coli
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Insert Size (bp)3686
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site PvuII (destroyed during cloning)
- 3′ cloning site PflMI (destroyed during cloning)
- 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 byhygromycin gene driven by the copia promoter from pMK33 (R. Nusse, Stanford University)
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:
pDrBB2 was a gift from Michele Calos (Addgene plasmid # 18946 ; http://n2t.net/addgene:18946 ; RRID:Addgene_18946) -
For your References section:
Construction of transgenic Drosophila by using the site-specific integrase from phage phiC31. Groth AC, Fish M, Nusse R, Calos MP. Genetics. 2004 Apr . 166(4):1775-82. 10.1534/genetics.166.4.1775 PubMed 15126397