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human embryonic kidney cell line 293 t  (ATCC)


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    ATCC human embryonic kidney cell line 293 t
    Human Embryonic Kidney Cell Line 293 T, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 38052 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+embryonic+kidney+cell+line+293+t/293T/pm41855715-39-22-34
    Average 99 stars, based on 38052 article reviews
    human embryonic kidney cell line 293 t - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Dimerization-dependent serine protease activity of FAM111A prevents replication fork stalling at topoisomerase 1 cleavage complexes
    Article Snippet: .. Human embryonic kidney cell line 293 T was purchased from American Type Culture Collection (#CRL-11268) and cultured in Dulbecco’s modified Eagle’s medium supplemented with 10% FBS. ..

    Modification:

    Article Title: Dimerization-dependent serine protease activity of FAM111A prevents replication fork stalling at topoisomerase 1 cleavage complexes
    Article Snippet: .. Human embryonic kidney cell line 293 T was purchased from American Type Culture Collection (#CRL-11268) and cultured in Dulbecco’s modified Eagle’s medium supplemented with 10% FBS. ..

    Multiple Displacement Amplification:

    Article Title: AEBP1 drives fibroblast-mediated T cell dysfunction in tumors
    Article Snippet: .. Murine colorectal carcinoma cell lines CT26 (CRL-2638), murine mammary carcinoma cell lines EO771 (CRL-3461), EMT6 (CRL-2755), and 4T1 (CRL-2539), human mammary cell line MDA-MB-231 (HTB-26), the melanoma cell line B16-F10 (CRL-6475), and human embryonic kidney cell line 293 T (CRL-3216) were all sourced from the American Type Culture Collection (ATCC). ..

    Article Title: AEBP1 drives fibroblast-mediated T cell dysfunction in tumors.
    Article Snippet: .. Murine colorectal carcinoma cell lines CT26 (CRL2638), murine mammary carcinoma cell lines EO771 (CRL-3461), EMT6 (CRL-2755), and 4T1 (CRL-2539), human mammary cell line MDA-MB231 (HTB-26), the melanoma cell line B16-F10 (CRL-6475), and human embryonic kidney cell line 293 T (CRL-3216) were all sourced from the American Type Culture Collection (ATCC). ..



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    https://www.bioz.com/product/human+embryonic+kidney+cell+line+293+t/293T/pm41855715-39-22-34
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    embryonic kidney 293 t cell line  (ATCC)
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    Preparation and characteristics of RVG-EVs@Echi. ( a ) Schematic illustration of the preparation process of RVG-EVs@Echi. ( b ) Representative fluorescence microscopy images of <t>293</t> <t>T</t> cells transduced with RVG lentivirus showing the infection efficiency. Scale bar: 200 nm. ( c ) Representative TEM image (inset) and size distribution of RVG-EVs@Echi. Scale bar: 100 nm. ( d ) Size distribution of free EVs and RVG-EVs. ( e ) Representative confocal images and ( f ) statistical analysis results showing the targeted delivery of RVG-EVs to neurons. sEVs are labeled with DiI (red), and neurons are labeled with alpha-tubulin (green). Nuclei are labeled with DAPI (blue). Scale bars, 50 μm for the original images and 10 μm for the magnified images. ( g ) Echi loading efficiency after room temperature incubation or electroporation. ( h ) Zeta potential of RVG-EVs and RVG-EVs@Echi, as measured by DLS. ( i ) Size distribution of RVG-EVs@Echi in PBS or in 20% FBS over time. ( j ) Free-EVs@Echi and RVG-EVs@Echi release curves of Echi over time. ( k ) Echi leakage rate of RVG-EVs@Echi over time. ( l ) Representative flow cytometry histograms and ( m ) quantitative time-course analysis of uptake (mean fluorescence intensity, MFI) by flow cytometry in MN9D cells incubated with DiI-labeled Free EVs or RVG-EVs for 3, 6, or 12 h. Data are shown as mean ± SEM. ** p < 0.01 vs. the Free EVs group
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    Preparation and characteristics of RVG-EVs@Echi. ( a ) Schematic illustration of the preparation process of RVG-EVs@Echi. ( b ) Representative fluorescence microscopy images of <t>293</t> <t>T</t> cells transduced with RVG lentivirus showing the infection efficiency. Scale bar: 200 nm. ( c ) Representative TEM image (inset) and size distribution of RVG-EVs@Echi. Scale bar: 100 nm. ( d ) Size distribution of free EVs and RVG-EVs. ( e ) Representative confocal images and ( f ) statistical analysis results showing the targeted delivery of RVG-EVs to neurons. sEVs are labeled with DiI (red), and neurons are labeled with alpha-tubulin (green). Nuclei are labeled with DAPI (blue). Scale bars, 50 μm for the original images and 10 μm for the magnified images. ( g ) Echi loading efficiency after room temperature incubation or electroporation. ( h ) Zeta potential of RVG-EVs and RVG-EVs@Echi, as measured by DLS. ( i ) Size distribution of RVG-EVs@Echi in PBS or in 20% FBS over time. ( j ) Free-EVs@Echi and RVG-EVs@Echi release curves of Echi over time. ( k ) Echi leakage rate of RVG-EVs@Echi over time. ( l ) Representative flow cytometry histograms and ( m ) quantitative time-course analysis of uptake (mean fluorescence intensity, MFI) by flow cytometry in MN9D cells incubated with DiI-labeled Free EVs or RVG-EVs for 3, 6, or 12 h. Data are shown as mean ± SEM. ** p < 0.01 vs. the Free EVs group
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    Preparation and characteristics of RVG-EVs@Echi. ( a ) Schematic illustration of the preparation process of RVG-EVs@Echi. ( b ) Representative fluorescence microscopy images of <t>293</t> <t>T</t> cells transduced with RVG lentivirus showing the infection efficiency. Scale bar: 200 nm. ( c ) Representative TEM image (inset) and size distribution of RVG-EVs@Echi. Scale bar: 100 nm. ( d ) Size distribution of free EVs and RVG-EVs. ( e ) Representative confocal images and ( f ) statistical analysis results showing the targeted delivery of RVG-EVs to neurons. sEVs are labeled with DiI (red), and neurons are labeled with alpha-tubulin (green). Nuclei are labeled with DAPI (blue). Scale bars, 50 μm for the original images and 10 μm for the magnified images. ( g ) Echi loading efficiency after room temperature incubation or electroporation. ( h ) Zeta potential of RVG-EVs and RVG-EVs@Echi, as measured by DLS. ( i ) Size distribution of RVG-EVs@Echi in PBS or in 20% FBS over time. ( j ) Free-EVs@Echi and RVG-EVs@Echi release curves of Echi over time. ( k ) Echi leakage rate of RVG-EVs@Echi over time. ( l ) Representative flow cytometry histograms and ( m ) quantitative time-course analysis of uptake (mean fluorescence intensity, MFI) by flow cytometry in MN9D cells incubated with DiI-labeled Free EVs or RVG-EVs for 3, 6, or 12 h. Data are shown as mean ± SEM. ** p < 0.01 vs. the Free EVs group
    293 T Embryonic Kidney Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+embryonic+kidney+cell+line+293+t/293T%3B+Embryonic+Kidney+Cells%3B+Human/pm41315184-299-2-11
    Average 99 stars, based on 1 article reviews
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    embryonic kidney hek 293 t cell line  (ATCC)
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    ATCC embryonic kidney hek 293 t cell line
    Preparation and characteristics of RVG-EVs@Echi. ( a ) Schematic illustration of the preparation process of RVG-EVs@Echi. ( b ) Representative fluorescence microscopy images of <t>293</t> <t>T</t> cells transduced with RVG lentivirus showing the infection efficiency. Scale bar: 200 nm. ( c ) Representative TEM image (inset) and size distribution of RVG-EVs@Echi. Scale bar: 100 nm. ( d ) Size distribution of free EVs and RVG-EVs. ( e ) Representative confocal images and ( f ) statistical analysis results showing the targeted delivery of RVG-EVs to neurons. sEVs are labeled with DiI (red), and neurons are labeled with alpha-tubulin (green). Nuclei are labeled with DAPI (blue). Scale bars, 50 μm for the original images and 10 μm for the magnified images. ( g ) Echi loading efficiency after room temperature incubation or electroporation. ( h ) Zeta potential of RVG-EVs and RVG-EVs@Echi, as measured by DLS. ( i ) Size distribution of RVG-EVs@Echi in PBS or in 20% FBS over time. ( j ) Free-EVs@Echi and RVG-EVs@Echi release curves of Echi over time. ( k ) Echi leakage rate of RVG-EVs@Echi over time. ( l ) Representative flow cytometry histograms and ( m ) quantitative time-course analysis of uptake (mean fluorescence intensity, MFI) by flow cytometry in MN9D cells incubated with DiI-labeled Free EVs or RVG-EVs for 3, 6, or 12 h. Data are shown as mean ± SEM. ** p < 0.01 vs. the Free EVs group
    Embryonic Kidney Hek 293 T Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+embryonic+kidney+cell+line+293+t/293T%3B+Embryonic+Kidney+Cells%3B+Human/pmc12749614-325-2-13
    Average 99 stars, based on 1 article reviews
    embryonic kidney hek 293 t cell line - by Bioz Stars, 2026-10
    99/100 stars
    		  Buy from Supplier

    Image Search Results


    Preparation and characteristics of RVG-EVs@Echi. ( a ) Schematic illustration of the preparation process of RVG-EVs@Echi. ( b ) Representative fluorescence microscopy images of 293 T cells transduced with RVG lentivirus showing the infection efficiency. Scale bar: 200 nm. ( c ) Representative TEM image (inset) and size distribution of RVG-EVs@Echi. Scale bar: 100 nm. ( d ) Size distribution of free EVs and RVG-EVs. ( e ) Representative confocal images and ( f ) statistical analysis results showing the targeted delivery of RVG-EVs to neurons. sEVs are labeled with DiI (red), and neurons are labeled with alpha-tubulin (green). Nuclei are labeled with DAPI (blue). Scale bars, 50 μm for the original images and 10 μm for the magnified images. ( g ) Echi loading efficiency after room temperature incubation or electroporation. ( h ) Zeta potential of RVG-EVs and RVG-EVs@Echi, as measured by DLS. ( i ) Size distribution of RVG-EVs@Echi in PBS or in 20% FBS over time. ( j ) Free-EVs@Echi and RVG-EVs@Echi release curves of Echi over time. ( k ) Echi leakage rate of RVG-EVs@Echi over time. ( l ) Representative flow cytometry histograms and ( m ) quantitative time-course analysis of uptake (mean fluorescence intensity, MFI) by flow cytometry in MN9D cells incubated with DiI-labeled Free EVs or RVG-EVs for 3, 6, or 12 h. Data are shown as mean ± SEM. ** p < 0.01 vs. the Free EVs group

    Journal: Journal of Nanobiotechnology

    Article Title: RVG-targeted extracellular vesicles loaded with echinatin attenuate dopaminergic neurodegeneration via the IGF-2/PI3K/Akt pathway in Parkinson’s disease mice

    doi: 10.1186/s12951-025-03997-5

    Figure Lengend Snippet: Preparation and characteristics of RVG-EVs@Echi. ( a ) Schematic illustration of the preparation process of RVG-EVs@Echi. ( b ) Representative fluorescence microscopy images of 293 T cells transduced with RVG lentivirus showing the infection efficiency. Scale bar: 200 nm. ( c ) Representative TEM image (inset) and size distribution of RVG-EVs@Echi. Scale bar: 100 nm. ( d ) Size distribution of free EVs and RVG-EVs. ( e ) Representative confocal images and ( f ) statistical analysis results showing the targeted delivery of RVG-EVs to neurons. sEVs are labeled with DiI (red), and neurons are labeled with alpha-tubulin (green). Nuclei are labeled with DAPI (blue). Scale bars, 50 μm for the original images and 10 μm for the magnified images. ( g ) Echi loading efficiency after room temperature incubation or electroporation. ( h ) Zeta potential of RVG-EVs and RVG-EVs@Echi, as measured by DLS. ( i ) Size distribution of RVG-EVs@Echi in PBS or in 20% FBS over time. ( j ) Free-EVs@Echi and RVG-EVs@Echi release curves of Echi over time. ( k ) Echi leakage rate of RVG-EVs@Echi over time. ( l ) Representative flow cytometry histograms and ( m ) quantitative time-course analysis of uptake (mean fluorescence intensity, MFI) by flow cytometry in MN9D cells incubated with DiI-labeled Free EVs or RVG-EVs for 3, 6, or 12 h. Data are shown as mean ± SEM. ** p < 0.01 vs. the Free EVs group

    Article Snippet: The 293 T human embryonic kidney cell line (acquired from ATCC) was cultured in Dulbecco’s modified Eagle’s medium (DMEM; Thermo Fisher Scientific) supplemented with 10% fetal bovine serum (FBS; Invitrogen).

    Techniques: Fluorescence, Microscopy, Transduction, Infection, Labeling, Incubation, Electroporation, Zeta Potential Analyzer, Flow Cytometry