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toronto human knockout pooled library tkov3  (Addgene inc)


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    Addgene inc toronto human knockout pooled library tkov3
    (A) Schematic representation of the screening protocol. HEK293T cells expressing GFP-Parkin R42P from the landing pad were transduced with the <t>TKOv3</t> sgRNA library. Fluorescence activated cells sorting (FACS) was used to collect the cells with the 5% highest and lowest GFP:mCherry ratios. Finally, the sgRNAs were identified by sequencing. Created in BioRender. Hartmann-Petersen, R. (2025) https://BioRender.com/mxx8owh . (B) Plot displaying sgRNA enrichment in the 5% highest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green. (C) Plot displaying sgRNA enrichment in the 5% lowest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green.
    Toronto Human Knockout Pooled Library Tkov3, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 81 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/toronto human knockout pooled library tkov3/product/Addgene inc
    Average 94 stars, based on 81 article reviews
    toronto human knockout pooled library tkov3 - by Bioz Stars, 2026-05
    94/100 stars

    Images

    1) Product Images from "BAG6 and RNF126 are broadly involved in protein quality control of non-native missense protein variants"

    Article Title: BAG6 and RNF126 are broadly involved in protein quality control of non-native missense protein variants

    Journal: bioRxiv

    doi: 10.64898/2026.02.04.703735

    (A) Schematic representation of the screening protocol. HEK293T cells expressing GFP-Parkin R42P from the landing pad were transduced with the TKOv3 sgRNA library. Fluorescence activated cells sorting (FACS) was used to collect the cells with the 5% highest and lowest GFP:mCherry ratios. Finally, the sgRNAs were identified by sequencing. Created in BioRender. Hartmann-Petersen, R. (2025) https://BioRender.com/mxx8owh . (B) Plot displaying sgRNA enrichment in the 5% highest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green. (C) Plot displaying sgRNA enrichment in the 5% lowest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green.
    Figure Legend Snippet: (A) Schematic representation of the screening protocol. HEK293T cells expressing GFP-Parkin R42P from the landing pad were transduced with the TKOv3 sgRNA library. Fluorescence activated cells sorting (FACS) was used to collect the cells with the 5% highest and lowest GFP:mCherry ratios. Finally, the sgRNAs were identified by sequencing. Created in BioRender. Hartmann-Petersen, R. (2025) https://BioRender.com/mxx8owh . (B) Plot displaying sgRNA enrichment in the 5% highest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green. (C) Plot displaying sgRNA enrichment in the 5% lowest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green.

    Techniques Used: Expressing, Transduction, Fluorescence, Sequencing, Control



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    (A) Schematic representation of the screening protocol. HEK293T cells expressing GFP-Parkin R42P from the landing pad were transduced with the <t>TKOv3</t> sgRNA library. Fluorescence activated cells sorting (FACS) was used to collect the cells with the 5% highest and lowest GFP:mCherry ratios. Finally, the sgRNAs were identified by sequencing. Created in BioRender. Hartmann-Petersen, R. (2025) https://BioRender.com/mxx8owh . (B) Plot displaying sgRNA enrichment in the 5% highest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green. (C) Plot displaying sgRNA enrichment in the 5% lowest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green.
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    Image Search Results


    (A) Schematic representation of the screening protocol. HEK293T cells expressing GFP-Parkin R42P from the landing pad were transduced with the TKOv3 sgRNA library. Fluorescence activated cells sorting (FACS) was used to collect the cells with the 5% highest and lowest GFP:mCherry ratios. Finally, the sgRNAs were identified by sequencing. Created in BioRender. Hartmann-Petersen, R. (2025) https://BioRender.com/mxx8owh . (B) Plot displaying sgRNA enrichment in the 5% highest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green. (C) Plot displaying sgRNA enrichment in the 5% lowest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green.

    Journal: bioRxiv

    Article Title: BAG6 and RNF126 are broadly involved in protein quality control of non-native missense protein variants

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    Figure Lengend Snippet: (A) Schematic representation of the screening protocol. HEK293T cells expressing GFP-Parkin R42P from the landing pad were transduced with the TKOv3 sgRNA library. Fluorescence activated cells sorting (FACS) was used to collect the cells with the 5% highest and lowest GFP:mCherry ratios. Finally, the sgRNAs were identified by sequencing. Created in BioRender. Hartmann-Petersen, R. (2025) https://BioRender.com/mxx8owh . (B) Plot displaying sgRNA enrichment in the 5% highest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green. (C) Plot displaying sgRNA enrichment in the 5% lowest GFP:mCherry bin. Significant (p < 0.001 and log2 fold change > 0.5) hits are colored red. Control sgRNAs are marked in green.

    Article Snippet: The Toronto human knockout pooled library (TKOv3) (Addgene #90294) , psPAX2 (Addgene #12260) and pMD2.G (Addgene #12259) were from Addgene.

    Techniques: Expressing, Transduction, Fluorescence, Sequencing, Control