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                <identifier>oai:data.mendeley.com/w24t4trkv5.2</identifier>
                <datestamp>2025-01-06T16:44:39Z</datestamp>
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    <dc:creator>Sato, Yohei</dc:creator>
    <dc:title>A dataset on NFKB1/NFKB2 knockout Jurkat cells and primary CD4+ T cells generated by CRISPR/Cas9 mediated gene disruption. </dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Specific biological roles of non-canonical nuclear factor-kappa B (NFKB) signaling in human T cells remain unclear. Therefore, we genetically modified Jurkat leukemic cells using the clustered regularly interspaced palindromic repeat (CRISPR)/CRISPR-associated protein 9 technology to better understand the NFKB signaling mechanisms. IKAROS family zinc finger-2 levels were downregulated in NFKB2-knocked-out cells but upregulated in NFKB1-knocked-out cells. To further understand the biological roles of NFKB signaling in CD4+ T cells, NFKB1/NFKB2 loci of human primary CD4+ T cells were genetically edited using the CRISPR/CRISPR-associated protein 9 technology. Quantitative polymerase chain reaction and fluorescence-activated cell sorting revealed the similar phenotypes and gene expression profiles of NFKB1/NFKB2-knocked-out human CD4+ T cells.</dc:description>
    <dc:subject>Immunology</dc:subject>
    <dc:subject>Biotechnology</dc:subject>
    <dc:subject>Genome Editing</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/w24t4trkv5.2</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/w24t4trkv5.2</dc:identifier>
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    <dc:date>2025-01-06T16:44:39Z</dc:date>
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