Fuw-AcrIIA4-P2A-GFP
(Plasmid
#108247)
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PurposeLentiviral vector to express AcrIIA4-P2A-GFP
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 108247 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneFuw
- Backbone size w/o insert (bp) 10043
- Total vector size (bp) 10331
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Modifications to backboneFuw-HA-P2A-EGFP
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Vector typeMammalian Expression, Lentiviral
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Selectable markersZeo marker is outside the LTRs and will not be packaged into virus
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature30°C
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Growth Strain(s)NEB Stable
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameAcrIIA4-NLS-HA
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SpeciesSynthetic
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Insert Size (bp)288
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Entrez GeneNEWENTRY
- Promoter Ubc
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Tag
/ Fusion Protein
- HA
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer aactatgcgctcggg
- 3′ sequencing primer taaagcagcgtatcc (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.
Depositor Comments
The sequence of AcrIIA4 was reported by Joseph Bondy-Denomy's laboratory "Inhibition of CRISPR-Cas9 with Bacteriophage Proteins", Cell, 2016.
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:
Fuw-AcrIIA4-P2A-GFP was a gift from Rudolf Jaenisch (Addgene plasmid # 108247 ; http://n2t.net/addgene:108247 ; RRID:Addgene_108247) -
For your References section:
Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 Gene. Liu XS, Wu H, Krzisch M, Wu X, Graef J, Muffat J, Hnisz D, Li CH, Yuan B, Xu C, Li Y, Vershkov D, Cacace A, Young RA, Jaenisch R. Cell. 2018 Feb 8. pii: S0092-8674(18)30049-7. doi: 10.1016/j.cell.2018.01.012. 10.1016/j.cell.2018.01.012 PubMed 29456084