pEGFP-IREShygro2
(Plasmid
#153966)
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PurposeExpresses EGFP in mammalian cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 153966 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepIREShyg2
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 5788
- Total vector size (bp) 6565
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Modifications to backboneN/A
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Vector typeMammalian 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 numberUnknown
Gene/Insert
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Gene/Insert nameEGFP
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Alt nameN/A
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SpeciesSynthetic
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Insert Size (bp)799
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MutationNo mutation
- Promoter CMV promoter
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Tag
/ Fusion Protein
- N/A
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NheI (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer -
- 3′ sequencing primer - (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byA NheI-BamHI fragment (containing EGFP) excised from pEGFP-C1 (Clontech) was inserted into the NheI-BamHI site of pIREShyg2 (Clontech)
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:
pEGFP-IREShygro2 was a gift from Hiroyuki Konishi (Addgene plasmid # 153966 ; http://n2t.net/addgene:153966 ; RRID:Addgene_153966) -
For your References section:
Tandem Paired Nicking Promotes Precise Genome Editing with Scarce Interference by p53. Hyodo T, Rahman ML, Karnan S, Ito T, Toyoda A, Ota A, Wahiduzzaman M, Tsuzuki S, Okada Y, Hosokawa Y, Konishi H. Cell Rep. 2020 Jan 28;30(4):1195-1207.e7. doi: 10.1016/j.celrep.2019.12.064. 10.1016/j.celrep.2019.12.064 PubMed 31995758