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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 37672 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCEFL
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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 numberUnknown
Gene/Insert
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Gene/Insert nameGli2
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SpeciesM. musculus (mouse)
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Entrez GeneGli2
- Promoter EF1a
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Tag
/ Fusion Protein
- mGFP (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site unknown (unknown if destroyed)
- 3′ cloning site unknown (unknown if destroyed)
- 5′ sequencing primer EF1a-Fwd
- 3′ sequencing primer BGH-Rev (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made bypCEFL was provided by J. Silvio Gutkind (National Institutes of Health).
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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
monomeric GFP was constructed by introducing the monomeric mutation, A206K, to EGFP.
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:
pCEFLmGFP-Gli2 was a gift from Philip Beachy (Addgene plasmid # 37672 ; http://n2t.net/addgene:37672 ; RRID:Addgene_37672) -
For your References section:
Gli2 trafficking links Hedgehog-dependent activation of Smoothened in the primary cilium to transcriptional activation in the nucleus. Kim J, Kato M, Beachy PA. Proc Natl Acad Sci U S A. 2009 Dec 22;106(51):21666-71. Epub 2009 Dec 8. 10.1073/pnas.0912180106 PubMed 19996169