pCMV-GLI(-)TAD
(Plasmid
#37113)
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Depositing Lab
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Publication
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Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 37113 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA3
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Backbone manufacturerInvitrogen
- Backbone size w/o insert (bp) 5500
- Total vector size (bp) 7700
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Modifications to backboneInserted GLI cDNA with a 1,409-bp AccI fragment deleted from the 3' end into the HindIII/XbaI site of pcDNA3.
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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)XL1 Blue
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameGLI1
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SpeciesH. sapiens (human)
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Mutationdeleted 1,409 bp AccI fragment from 3' end of GLI cDNA
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Entrez GeneGLI1 (a.k.a. GLI, PAPA8, PPD1)
- Promoter CMV
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site XbaI (not destroyed)
- 5′ sequencing primer CMV-
- 3′ sequencing primer --- (Common Sequencing Primers)
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:
pCMV-GLI(-)TAD was a gift from David Walterhouse (Addgene plasmid # 37113 ; http://n2t.net/addgene:37113 ; RRID:Addgene_37113) -
For your References section:
GLI activates transcription through a herpes simplex viral protein 16-like activation domain. Yoon JW, Liu CZ, Yang JT, Swart R, Iannaccone P, Walterhouse D. J Biol Chem. 1998 Feb 6;273(6):3496-501. 10.1074/jbc.273.6.3496 PubMed 9452474