GFP-LacI-Cyclin B1 ND
(Plasmid
#234706)
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Purposeallows tethering of non degradable (ND) cyclin B1 protein to lacO repeats in specific chromatin loci
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 234706 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneGFP-LacI-polylinker
- Backbone size w/o insert (bp) 7307
- Total vector size (bp) 8586
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
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 nameCyclin B1
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SpeciesH. sapiens (human)
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Insert Size (bp)1300
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Entrez GeneCCNB1 (a.k.a. CCNB)
- Promoter CMV
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer EGFP
- 3′ sequencing primer bGH polyA reverse (Common Sequencing Primers)
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:
GFP-LacI-Cyclin B1 ND was a gift from Lienhard Schmitz (Addgene plasmid # 234706 ; http://n2t.net/addgene:234706 ; RRID:Addgene_234706) -
For your References section:
CDK1-mediated phosphorylation at H2B serine 6 is required for mitotic chromosome segregation. Seibert M, Kruger M, Watson NA, Sen O, Daum JR, Slotman JA, Braun T, Houtsmuller AB, Gorbsky GJ, Jacob R, Kracht M, Higgins JMG, Schmitz ML. J Cell Biol. 2019 Apr 1;218(4):1164-1181. doi: 10.1083/jcb.201806057. Epub 2019 Feb 14. 10.1083/jcb.201806057 PubMed 30765437