XNM-Luc
(Plasmid
#35157)
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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 | 35157 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepGL2-basic
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Backbone manufacturerPromega
- Backbone size w/o insert (bp) 5597
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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 nameMyc promoter
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SpeciesH. sapiens (human)
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Insert Size (bp)152
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MutationContains 152 bp of the myc promoter
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Entrez GeneMYC (a.k.a. MRTL, MYCC, bHLHe39, c-Myc)
- Promoter c-myc
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Tag
/ Fusion Protein
- Luciferase (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site XhoI (not destroyed)
- 3′ cloning site BglII (destroyed during cloning)
- 5′ sequencing primer n/a
- 3′ sequencing primer Luc_N_Rev (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byOriginal construct in pBluescript was from E. Laufer
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
This plasmid is a c-myc promoter-luciferase reporter construct designed to examine the regulation of transcription in response to conditional and constitutive Myc activation and functions as described in the associated publication.
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:
XNM-Luc was a gift from Linda Penn (Addgene plasmid # 35157 ; http://n2t.net/addgene:35157 ; RRID:Addgene_35157) -
For your References section:
The Myc negative autoregulation mechanism requires Myc-Max association and involves the c-myc P2 minimal promoter. Facchini LM, Chen S, Marhin WW, Lear JN, Penn LZ. Mol Cell Biol. 1997 Jan;17(1):100-14. PubMed 8972190