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PurposeHIV-1 transfer vector, encodes firefly luciferase gene interrupted by a gamma-globin intron. The reporter gene is silent in the transfected cells and expressed in the infected cells.
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Depositing Labs
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 58955 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepUCHR
- Backbone size w/o insert (bp) 5753
- Total vector size (bp) 9442
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Vector typeLentiviral
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)Stbl2
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameinLuc
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Insert Size (bp)3689
- Promoter CMV
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRV (not destroyed)
- 3′ cloning site XmaI (not destroyed)
- 5′ sequencing primer none
- 3′ sequencing primer none (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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:
pUCHR-inLuc was a gift from David Derse & Dmitriy Mazurov (Addgene plasmid # 58955 ; http://n2t.net/addgene:58955 ; RRID:Addgene_58955) -
For your References section:
Quantitative comparison of HTLV-1 and HIV-1 cell-to-cell infection with new replication dependent vectors. Mazurov D, Ilinskaya A, Heidecker G, Lloyd P, Derse D. PLoS Pathog. 2010 Feb 26;6(2):e1000788. doi: 10.1371/journal.ppat.1000788. 10.1371/journal.ppat.1000788 PubMed 20195464