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episomal vector  (Addgene inc)


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    Structured Review

    Addgene inc episomal vector
    Episomal Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 30 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/px458+aavs1/PX458-AAVS1+(Plasmid+%23113194)/10__34133_slash_research__1241-227-9-12
    Average 93 stars, based on 30 article reviews
    episomal vector - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: miR126-mediated impaired vascular integrity in Rett syndrome
    Article Snippet: .. PX458-AAVS1 was a gift from Adam Karpf (Addgene plasmid #113194; http://n2t.net/addgene:113194 ; RRID:Addgene_113194) and pUCM-AAVS1-TO-hNGN2 was a gift from Michael Ward (Addgene plasmid # 105840; http://n2t.net/addgene:105840 ; RRID:Addgene_105840). .. DNA were collected from genome edited iPS cells by QIAamp DNA kit (Qiagen).

    Article Title: miR126-mediated alteration of vascular integrity in Rett syndrome.
    Article Snippet: .. PX458-AAVS1 was a gift from Adam Karpf (Addgene plasmid #113194; http://n2t.net/addgene:113194; RRID:Addgene_113194) and pUCM-AAVS1TO-hNGN2 was a gift from Michael Ward (Addgene plasmid # 105840; http://n2t.net/addgene:105840; RRID:Addgene_105840). .. DNA was collected from genome-edited iPS cells using a QIAamp DNA Kit (Qiagen).

    Article Title: The PST repeat region of MDC1 is a tunable multivalent chromatin tethering domain
    Article Snippet: To knock-in inducible WT and T>A GFP-PST-LacI fusion proteins into the AAVS1 locus in U2OS 2-6-3 cells, we PCR amplified GFP and LacI from a GFP-LacI expression plasmid (a kind gift from Iain Cheeseman) 68 and codon-optimized WT and T>A PST repeat sequences and cloned them by Gibson assembly into MluI and SalI-linearized AAVS1-TRE3G-EGFP (a gift from Su-Chun Zhang (Addgene plasmid # 52343)) . .. The AAVS1-targeting gRNA plasmid, PX458-AAVS1, was a gift from Adam Karpf (Addgene plasmid # 113194). .. To express and purify GST-tagged PST repeats from E. coli, two gBlocks for each protein fragment were codon-optimized for expression in E. coli and were cloned by Gibson assembly into BamHI-linearized pGSTag (a gift from David Ron, (Addgene plasmid # 21877) .

    Over Expression:

    Article Title: ZMYND11 functions in bimodal regulation of latent genes and brain-like splicing to safeguard corticogenesis.
    Article Snippet: .. Generation of doxycycline inducible ZMYND11 overexpression lines In experiments where we overexpressed the wildtype ZMYND11 construct, PX458-AAVS1 (Addgene #113194) and AAVS1-Neo-M2rtTA (Addgene #60843) were nucleofected into 3 million cells by LONZA 4D-Nucleofector using program CB-150. ..

    Construct:

    Article Title: ZMYND11 functions in bimodal regulation of latent genes and brain-like splicing to safeguard corticogenesis.
    Article Snippet: .. Generation of doxycycline inducible ZMYND11 overexpression lines In experiments where we overexpressed the wildtype ZMYND11 construct, PX458-AAVS1 (Addgene #113194) and AAVS1-Neo-M2rtTA (Addgene #60843) were nucleofected into 3 million cells by LONZA 4D-Nucleofector using program CB-150. ..

    Article Title: ZMYND11 Functions in Bimodal Regulation of Latent Genes and Brain-like Splicing to Safeguard Corticogenesis
    Article Snippet: .. In experiments where we overexpressed the wildtype ZMYND11 construct, PX458-AAVS1 (Addgene #113194) and AAVS1-Neo-M2rtTA (Addgene #60843) were nucleofected into 3 million cells by LONZA 4D-Nucleofector using program CB-150. ..

    Article Title: ZMYND11 functions in bimodal regulation of latent genes and brain-like splicing to safeguard corticogenesis
    Article Snippet: .. In experiments where we overexpressed the wildtype ZMYND11 construct, PX458-AAVS1 (Addgene #113194) and AAVS1-Neo-M2rtTA (Addgene #60843) were nucleofected into 3 million cells by LONZA 4D-Nucleofector using program CB-150. ..

    Transfection:

    Article Title: The Generation of Genetically Engineered Human Induced Pluripotent Stem Cells Overexpressing IFN-β for Future Experimental and Clinically Oriented Studies
    Article Snippet: On the next day, the cells were dissociated using the TrypLE Express Enzyme (Thermo Fisher Scientific), and counted, and 10 6 cells were transfected using the NeonTM Transfection System 100 μL Kit (Invitrogen, Waltham, MA, USA) according to the manufacturer’s instructions (NeonTM NxT Electroporation System, InvitrogenTM, Thermo Fisher Scientific, Waltham, MA, USA; one pulse, 30 ms, 1100 V). .. The plasmids used for the transfection were as follows: pAAVS1-hPGK-IFNB1 (expressing the human IFNB ORF) and pX458-AAVS1 (Addgene, expressing SpCas9 nuclease, EGFP, and sgRNA targeting the human AAVS1 locus [ ]). .. After the transfection, the cells were seeded on MEF-coated 10 cm 2 Petri dishes (Corning) in the iPSC medium containing thiazovivin but without the addition of penicillin/streptomycin.

    Expressing:

    Article Title: The Generation of Genetically Engineered Human Induced Pluripotent Stem Cells Overexpressing IFN-β for Future Experimental and Clinically Oriented Studies
    Article Snippet: On the next day, the cells were dissociated using the TrypLE Express Enzyme (Thermo Fisher Scientific), and counted, and 10 6 cells were transfected using the NeonTM Transfection System 100 μL Kit (Invitrogen, Waltham, MA, USA) according to the manufacturer’s instructions (NeonTM NxT Electroporation System, InvitrogenTM, Thermo Fisher Scientific, Waltham, MA, USA; one pulse, 30 ms, 1100 V). .. The plasmids used for the transfection were as follows: pAAVS1-hPGK-IFNB1 (expressing the human IFNB ORF) and pX458-AAVS1 (Addgene, expressing SpCas9 nuclease, EGFP, and sgRNA targeting the human AAVS1 locus [ ]). .. After the transfection, the cells were seeded on MEF-coated 10 cm 2 Petri dishes (Corning) in the iPSC medium containing thiazovivin but without the addition of penicillin/streptomycin.



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