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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 | 19290 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepGL2Basic
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Backbone manufacturerPromega
- Backbone size w/o insert (bp) 5568
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Vector typeMammalian Expression, Luciferase
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 nameE-cadherin
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SpeciesH. sapiens (human)
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Insert Size (bp)233
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MutationE-cad promoter sequences from -108 to +125
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SacI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer unknown
- 3′ sequencing primer luc-rev (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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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
Endogenous ATG of Ecad destroyed; "C" deleted 5 bp 5' of ATG (the destroyed one)
33 bp linker between Ecad promoter and luciferace gene.
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:
pGL2Basic-EcadK1 was a gift from Eric Fearon (Addgene plasmid # 19290 ; http://n2t.net/addgene:19290 ; RRID:Addgene_19290) -
For your References section:
Extinction of E-cadherin expression in breast cancer via a dominant repression pathway acting on proximal promoter elements. Hajra KM, Ji X, Fearon ER. Oncogene. 1999 Dec 2. 18(51):7274-9. 10.1038/sj.onc.1203336 PubMed 10602481