pmCherry-TdIF2
(Plasmid
#196906)
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Purposevisualization of TdIF2/ERBP as a fusion to mCherry
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 196906 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepEGFP-C1
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 4700
- Total vector size (bp) 6800
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Modifications to backboneOur pmCherry C-1 was constructed by replacing Nhe I-Bgl II EGFP fragment with Nhe I-Bgl II 700bp mCherry DNA fragment, amplified by PCR using pRSET-B mCherry (provided by Prof. Roger Y. Tsien, University of California, San Diego) as a template. So, no AgeI site at 5’ nor BspE I site at 3’.
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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)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberUnknown
Gene/Insert
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Gene/Insert nameTdIF2
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Alt nameERBP
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Alt nameAB_046574
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SpeciesH. sapiens (human)
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Insert Size (bp)2100
- Promoter CMV
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Tag
/ Fusion Protein
- mCherry (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site Hind III (unknown if destroyed)
- 3′ cloning site Sal I (unknown if destroyed)
- 5′ sequencing primer EGFP side
- 3′ sequencing primer SV40 poly A side (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byObtained by screening the human cDNA library (purchased from Origene). mCherry C-1 was amplified by PCR using pRSET-B mCherry (provided by Prof. Roger Y. Tsien, University of California, San Diego) as a template.
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
2.1 kb PCR fragment of a pJG4-5 clone from OriGene human MCF7 cDNA library, was cloned the same sites of pEGFP-C1 and our original “pmCherry C-1” (without Eco47III, AgeI, BspEI sites).
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:
pmCherry-TdIF2 was a gift from Kenji Sugimoto (Addgene plasmid # 196906 ; http://n2t.net/addgene:196906 ; RRID:Addgene_196906) -
For your References section:
Characterization of nucleolar localization and exclusion signals in terminal deoxynucleotidyltransferase interacting factor 2/estrogen receptor alpha-binding protein. Fukada T, Shibata S, Ueda T, Sasaki K, Shimoida Y, Senda-Murata K, Sugimoto K. Biosci Biotechnol Biochem. 2019 Jul;83(7):1255-1262. doi: 10.1080/09168451.2019.1591265. Epub 2019 Mar 24. 10.1080/09168451.2019.1591265 PubMed 30907250