pCI-6.22
(Plasmid
#41087)
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Depositing Lab
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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 | 41087 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepGL3-Enhancer
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Backbone manufacturerPromega
- Backbone size w/o insert (bp) 5064
- Total vector size (bp) 6200
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Modifications to backboneThe STOP codon of FLuc was removed and replaced by an in-frame EcoRI site.
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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 nameGSG-P2A-RLuc
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Insert Size (bp)1014
- Promoter Promoterless
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer RVprimer3
- 3′ sequencing primer EBV-Rev (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.
Depositor Comments
This pCI-6.22 is a promoterless version of FLuc-P2A-RLuc coincident reporter plasmid. It contains a MCS in the 5' region for people to study their favorite promoter/response element. Please check the map of pGL3-Enhancer (Promega) for the infomation about the MCS.
Please note that the E304V point mutation found in the Addgene sequence does not affect the activity of this plasmid.
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:
pCI-6.22 was a gift from James Inglese (Addgene plasmid # 41087 ; http://n2t.net/addgene:41087 ; RRID:Addgene_41087) -
For your References section:
A coincidence reporter-gene system for high-throughput screening. Cheng KC, Inglese J. Nat Methods. 2012 Oct;9(10):937. doi: 10.1038/nmeth.2170. 10.1038/nmeth.2170 PubMed 23018994