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non targeting nt control sgrna  (Addgene inc)


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    Structured Review

    Addgene inc non targeting nt control sgrna
    Non Targeting Nt Control Sgrna, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 5733 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/non targeting nt control sgrna/product/Addgene inc
    Average 96 stars, based on 5733 article reviews
    non targeting nt control sgrna - by Bioz Stars, 2026-05
    96/100 stars

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    Addgene inc non targeting sgrna
    (A) Schematic workflow of the CRISPR screen approach. OCAB reporter cells are created through mOrange-P2A knock-in, transduced with the genome-wide <t>sgRNA</t> library Brunello, and FACS-sorted to identify the activators and repressors of OCAB expression. (B) Distribution of OCAB activators ranked by the RRA score. Selected activators were individually validated with specific targeting sgRNAs. A total of 113 hits were tested with 74 true positives. (C) mO-OCAB expression measured by flow cytometry 10 days after FLI1 or control sgRNA transduction. (D) ChIP-seq (FLI1, BRD4) and RNA-seq profiles at the OCAB locus in control and FLI1-depleted cells. Fold change and adjusted p values (Benjamini-Hochberg) are indicated. (E) As in (C) but after SPEN or control sgRNA transduction.
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    (A) Schematic workflow of the CRISPR screen approach. OCAB reporter cells are created through mOrange-P2A knock-in, transduced with the genome-wide sgRNA library Brunello, and FACS-sorted to identify the activators and repressors of OCAB expression. (B) Distribution of OCAB activators ranked by the RRA score. Selected activators were individually validated with specific targeting sgRNAs. A total of 113 hits were tested with 74 true positives. (C) mO-OCAB expression measured by flow cytometry 10 days after FLI1 or control sgRNA transduction. (D) ChIP-seq (FLI1, BRD4) and RNA-seq profiles at the OCAB locus in control and FLI1-depleted cells. Fold change and adjusted p values (Benjamini-Hochberg) are indicated. (E) As in (C) but after SPEN or control sgRNA transduction.

    Journal: Cell reports

    Article Title: Biphasic control of the B cell transcriptome by mTORC1 and GSK3

    doi: 10.1016/j.celrep.2025.116361

    Figure Lengend Snippet: (A) Schematic workflow of the CRISPR screen approach. OCAB reporter cells are created through mOrange-P2A knock-in, transduced with the genome-wide sgRNA library Brunello, and FACS-sorted to identify the activators and repressors of OCAB expression. (B) Distribution of OCAB activators ranked by the RRA score. Selected activators were individually validated with specific targeting sgRNAs. A total of 113 hits were tested with 74 true positives. (C) mO-OCAB expression measured by flow cytometry 10 days after FLI1 or control sgRNA transduction. (D) ChIP-seq (FLI1, BRD4) and RNA-seq profiles at the OCAB locus in control and FLI1-depleted cells. Fold change and adjusted p values (Benjamini-Hochberg) are indicated. (E) As in (C) but after SPEN or control sgRNA transduction.

    Article Snippet: For this, selected sgRNAs and a non-targeting sgRNA from the Brunello library were cloned into lentiGuide-puro (Addgene).

    Techniques: CRISPR, Knock-In, Transduction, Genome Wide, Expressing, Flow Cytometry, Control, ChIP-sequencing, RNA Sequencing