LeGO-iG2-wPRE-pA
(Plasmid
#60489)
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PurposeeGFP-expressing lentiviral vector with IRES and pA-signal; suitable for use as NRTLV (non-reverse transcribable lentiviral vector)
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 60489 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneLeGO
- Total vector size (bp) 8076
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Modifications to backboneInsertion of BGH-pA (polyadenylation-signal of bovine growth hormone)into PvuII-site of previously described LeGO-iG2. BGH-pA-fragment was generated by PCR using the following primer (u58-fw: GCTGTACAAGTAACTGTGCCTTCTAG and u59-rev: GCTGTACAGCCATAGAGCCCAC).
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Vector typeMammalian Expression, Lentiviral
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)Stbl3
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Growth instructionsany (like TOP10, XL10-Gold or Stbl)
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameIRES-eGFP; wPRE; BGH-pA
Resource Information
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A portion of this plasmid was derived from a plasmid made byAs template for BGH-pA-PCR the previously described pAC_CMV_TALE_RM1_long_FokI_1317 was used (Mussolino, C. et al. A novel TALE nuclease scaffold enables high genome editing activity in combination with low toxicity. Nucleic Acids Res.39,9283–9293 (2011))
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:
LeGO-iG2-wPRE-pA was a gift from Boris Fehse (Addgene plasmid # 60489 ; http://n2t.net/addgene:60489 ; RRID:Addgene_60489) -
For your References section:
Novel lentiviral vectors with mutated reverse transcriptase for mRNA delivery of TALE nucleases. Mock U, Riecken K, Berdien B, Qasim W, Chan E, Cathomen T, Fehse B. Sci Rep. 2014 Sep 18;4:6409. doi: 10.1038/srep06409. 10.1038/srep06409 PubMed 25230987