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empty crispri plasmid  (Addgene inc)


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    Structured Review

    Addgene inc empty crispri plasmid
    KEY RESOURCES TABLE
    Empty Crispri Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 242 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/empty+crispri+plasmid/pmc08800389-975-0-22?v=Addgene+inc
    Average 96 stars, based on 242 article reviews
    empty crispri plasmid - by Bioz Stars, 2026-07
    96/100 stars

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    1) Product Images from "Mutations in spliceosomal genes PPIL1 and PRP17 cause neurodegenerative pontocerebellar hypoplasia with microcephaly"

    Article Title: Mutations in spliceosomal genes PPIL1 and PRP17 cause neurodegenerative pontocerebellar hypoplasia with microcephaly

    Journal: Neuron

    doi: 10.1016/j.neuron.2020.10.035

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

    Techniques Used: Virus, Recombinant, Flow Cytometry, cDNA Synthesis, RNAscope, Multiplex Assay, Control, Knock-Out, Knock-In, Mutagenesis, Plasmid Preparation, Software



    Similar Products

    empty crispri plasmid  (Addgene inc)
    96
    Addgene inc empty crispri plasmid
    KEY RESOURCES TABLE
    Empty Crispri Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/empty+crispri+plasmid/pmc08800389-975-0-22?v=Addgene+inc
    Average 96 stars, based on 1 article reviews
    empty crispri plasmid - by Bioz Stars, 2026-07
    96/100 stars
    		  Buy from Supplier

    Image Search Results


    KEY RESOURCES TABLE

    Journal: Neuron

    Article Title: Mutations in spliceosomal genes PPIL1 and PRP17 cause neurodegenerative pontocerebellar hypoplasia with microcephaly

    doi: 10.1016/j.neuron.2020.10.035

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Empty CRISPRi plasmid (PX330-U6–2XBsmBI-gRNA-CBh-dCas9-KRAB-T2a-Puro) was generated on the modified PX330 with 2× BsmBI gRNA cloning sites. dCas9-KRAB-T2a-Puro was amplified from vector pLV-hU6-sgRNA-hUbC-dCas9-KRAB-T2aPuro (Addgene #71236) and cloned inside PX330 to replace original WT Cas9. gRNAs targeting PRP17 or scramble gRNA was further cloned between 2XBsmBI sites.

    Techniques: Virus, Recombinant, Flow Cytometry, cDNA Synthesis, RNAscope, Multiplex Assay, Control, Knock-Out, Knock-In, Mutagenesis, Plasmid Preparation, Software