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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 | 26063 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepmCherry-N1
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Backbone manufacturerSee note below
- Backbone size w/o insert (bp) 4700
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Vector typeMammalian Expression
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 nameCyclin B1
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SpeciesH. sapiens (human)
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Entrez GeneCCNB1 (a.k.a. CCNB)
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Tag
/ Fusion Protein
- mcherry (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer CMV-F
- 3′ sequencing primer mCherry-R (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
The backbone was derived from pECFP-N1. ECFP was replaced with mCherry.
There is a V5A mutation in cycB1. The mutation does not affect localization of the protein or it's degradation.
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:
p-cyclinB1-mcherry (1958) was a gift from Jonathon Pines (Addgene plasmid # 26063 ; http://n2t.net/addgene:26063 ; RRID:Addgene_26063) -
For your References section:
Progressive activation of CyclinB1-Cdk1 coordinates entry to mitosis. Gavet O, Pines J. Dev Cell. 2010 Apr 20. 18(4):533-43. 10.1016/j.devcel.2010.02.013 PubMed 20412769