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PurposeSplit GFP assay
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 68715 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepQCXIP
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Backbone manufacturerClontech
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Modifications to backboneGFP1-10 was amplified by PCR. The PCR product was ligated into BamHI/EcoRI site of pQCXIP-POU5 (created by insertion of POU5 into NotI/BamHI sites of pQCXIP). pQCXIP-POU5-GFP1-10 was digested with NotI/BamHI, filled in, and religated to remove POU5 resulting in pQCXIP-GFP1-10.
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Vector typeMammalian Expression, Retroviral
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Selectable markersPuromycin
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)Top10
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameGFP1-10
- Promoter CMV
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (unknown if destroyed)
- 3′ cloning site EcoRI (unknown if destroyed)
- 5′ sequencing primer LNCX
- 3′ sequencing primer IRES-R (Common Sequencing Primers)
Resource Information
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Addgene Notes
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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
GFP1-10 covers the first to the 10th beta strands of GFP.
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:
pQCXIP-GFP1-10 was a gift from Yutaka Hata (Addgene plasmid # 68715 ; http://n2t.net/addgene:68715 ; RRID:Addgene_68715) -
For your References section:
A new cell-based assay to evaluate myogenesis in mouse myoblast C2C12 cells. Kodaka M, Yang Z, Nakagawa K, Maruyama J, Xu X, Sarkar A, Ichimura A, Nasu Y, Ozawa T, Iwasa H, Ishigami-Yuasa M, Ito S, Kagechika H, Hata Y. Exp Cell Res. 2015 Aug 15;336(2):171-81. doi: 10.1016/j.yexcr.2015.06.015. Epub 2015 Jun 24. 10.1016/j.yexcr.2015.06.015 PubMed 26116467