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hek293 human embryonic kidney derived cells  (ATCC)


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    Structured Review

    ATCC hek293 human embryonic kidney derived cells
    Evaluation of structural modifications of nsEVs after sodium carbonate treatment. Transmission electron microscopy (TEM) image ( A ) and nanoparticle tracking analysis ( B ) of <t>HEK293-derived</t> nsEVs after sodium carbonate treatment. Western blot analysis ( C ) of Alix, TSG101, CD63 and CD9 before (pre) and after (post) sodium carbonate treatment. Comparison of nsEVs treated with phosphate buffer saline (PBS) or sodium carbonate (Na 2 CO 3 ) through silver staining ( D ) single-particle interferometric reflectance imaging sensor (SP-IRIS) analysis (E) and Raman spectroscopy (F). M: molecular weight marker
    Hek293 Human Embryonic Kidney Derived Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 21992 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+embryonic+kidney+derived+hek293/pmc11063024-161-0-8?v=ATCC
    Average 99 stars, based on 21992 article reviews
    hek293 human embryonic kidney derived cells - by Bioz Stars, 2026-07
    99/100 stars

    Images

    1) Product Images from "Novel loading protocol combines highly efficient encapsulation of exogenous therapeutic toxin with preservation of extracellular vesicles properties, uptake and cargo activity"

    Article Title: Novel loading protocol combines highly efficient encapsulation of exogenous therapeutic toxin with preservation of extracellular vesicles properties, uptake and cargo activity

    Journal: Discover Nano

    doi: 10.1186/s11671-024-04022-8

    Evaluation of structural modifications of nsEVs after sodium carbonate treatment. Transmission electron microscopy (TEM) image ( A ) and nanoparticle tracking analysis ( B ) of HEK293-derived nsEVs after sodium carbonate treatment. Western blot analysis ( C ) of Alix, TSG101, CD63 and CD9 before (pre) and after (post) sodium carbonate treatment. Comparison of nsEVs treated with phosphate buffer saline (PBS) or sodium carbonate (Na 2 CO 3 ) through silver staining ( D ) single-particle interferometric reflectance imaging sensor (SP-IRIS) analysis (E) and Raman spectroscopy (F). M: molecular weight marker
    Figure Legend Snippet: Evaluation of structural modifications of nsEVs after sodium carbonate treatment. Transmission electron microscopy (TEM) image ( A ) and nanoparticle tracking analysis ( B ) of HEK293-derived nsEVs after sodium carbonate treatment. Western blot analysis ( C ) of Alix, TSG101, CD63 and CD9 before (pre) and after (post) sodium carbonate treatment. Comparison of nsEVs treated with phosphate buffer saline (PBS) or sodium carbonate (Na 2 CO 3 ) through silver staining ( D ) single-particle interferometric reflectance imaging sensor (SP-IRIS) analysis (E) and Raman spectroscopy (F). M: molecular weight marker

    Techniques Used: Transmission Assay, Electron Microscopy, Derivative Assay, Western Blot, Comparison, Saline, Silver Staining, Single Particle, Imaging, Raman Spectroscopy, Molecular Weight, Marker

    Encapsulation efficiency evaluation and comparison between electroporation and sodium carbonate treatment. A Spectrofluorometer analysis for quantification of Dextran-FITC incorporation after 50 V electroporation (see material and methods) or sodium carbonate treatment of HEK293-derived nsEVs (25 µg/ml) in various nsEVs:Dextran-FITC ratios (1:1, 1:1.5 and 1:2). B Confocal microscopy images of Hela cells treated for 24 h with Dextran-FITC bearing nsEVs (25 µg/ml) after electroporation (50 V) or sodium carbonate incubation in NsEVs:Dextran-FITC = 1:1.5 molecular ratio (blue = DAPI; green = Dextran-FITC bearing nsEVs). C Spectrofluorometer analysis for quantification of SAP-FITC incorporation after 50 V electroporation (see material and methods) or sodium carbonate treatment of HEK293-derived nsEVs (25 µg/ml) in nsEVs:SAP-FITC = 1:1.5 ratio
    Figure Legend Snippet: Encapsulation efficiency evaluation and comparison between electroporation and sodium carbonate treatment. A Spectrofluorometer analysis for quantification of Dextran-FITC incorporation after 50 V electroporation (see material and methods) or sodium carbonate treatment of HEK293-derived nsEVs (25 µg/ml) in various nsEVs:Dextran-FITC ratios (1:1, 1:1.5 and 1:2). B Confocal microscopy images of Hela cells treated for 24 h with Dextran-FITC bearing nsEVs (25 µg/ml) after electroporation (50 V) or sodium carbonate incubation in NsEVs:Dextran-FITC = 1:1.5 molecular ratio (blue = DAPI; green = Dextran-FITC bearing nsEVs). C Spectrofluorometer analysis for quantification of SAP-FITC incorporation after 50 V electroporation (see material and methods) or sodium carbonate treatment of HEK293-derived nsEVs (25 µg/ml) in nsEVs:SAP-FITC = 1:1.5 ratio

    Techniques Used: Encapsulation, Comparison, Electroporation, Derivative Assay, Confocal Microscopy, Incubation

    Evaluation of sodium carbonate-treated SAP-bearing nsEVs uptake. A Bright field (upper row) and fluorescent (lower row) microscopy images of 5637 cells 24 h after incubation with HEK293-derived nsEVs treated with phosphate buffer saline (PBS, left) or sodium carbonate (Na 2 CO 3 , right) in the presence of SAP and stained with Vybrant Dio lipophilic dye. Different concentrations of nsEVs (5 and 10 µg) were used for comparison. Representative images of three independent experiments. B Flow cytometry analysis of 5637 cells 24 h after treatment with 5 or 10 µg of PBS or Na 2 CO 3 -treated SAP-bearing nsEVs. Results are shown as mean fluorescence percentage + SD from 3 independent experiments
    Figure Legend Snippet: Evaluation of sodium carbonate-treated SAP-bearing nsEVs uptake. A Bright field (upper row) and fluorescent (lower row) microscopy images of 5637 cells 24 h after incubation with HEK293-derived nsEVs treated with phosphate buffer saline (PBS, left) or sodium carbonate (Na 2 CO 3 , right) in the presence of SAP and stained with Vybrant Dio lipophilic dye. Different concentrations of nsEVs (5 and 10 µg) were used for comparison. Representative images of three independent experiments. B Flow cytometry analysis of 5637 cells 24 h after treatment with 5 or 10 µg of PBS or Na 2 CO 3 -treated SAP-bearing nsEVs. Results are shown as mean fluorescence percentage + SD from 3 independent experiments

    Techniques Used: Microscopy, Incubation, Derivative Assay, Saline, Staining, Comparison, Flow Cytometry, Fluorescence



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    Image Search Results


    Evaluation of structural modifications of nsEVs after sodium carbonate treatment. Transmission electron microscopy (TEM) image ( A ) and nanoparticle tracking analysis ( B ) of HEK293-derived nsEVs after sodium carbonate treatment. Western blot analysis ( C ) of Alix, TSG101, CD63 and CD9 before (pre) and after (post) sodium carbonate treatment. Comparison of nsEVs treated with phosphate buffer saline (PBS) or sodium carbonate (Na 2 CO 3 ) through silver staining ( D ) single-particle interferometric reflectance imaging sensor (SP-IRIS) analysis (E) and Raman spectroscopy (F). M: molecular weight marker

    Journal: Discover Nano

    Article Title: Novel loading protocol combines highly efficient encapsulation of exogenous therapeutic toxin with preservation of extracellular vesicles properties, uptake and cargo activity

    doi: 10.1186/s11671-024-04022-8

    Figure Lengend Snippet: Evaluation of structural modifications of nsEVs after sodium carbonate treatment. Transmission electron microscopy (TEM) image ( A ) and nanoparticle tracking analysis ( B ) of HEK293-derived nsEVs after sodium carbonate treatment. Western blot analysis ( C ) of Alix, TSG101, CD63 and CD9 before (pre) and after (post) sodium carbonate treatment. Comparison of nsEVs treated with phosphate buffer saline (PBS) or sodium carbonate (Na 2 CO 3 ) through silver staining ( D ) single-particle interferometric reflectance imaging sensor (SP-IRIS) analysis (E) and Raman spectroscopy (F). M: molecular weight marker

    Article Snippet: HEK293 (human embryonic kidney-derived) cells were purchased from ATCC.

    Techniques: Transmission Assay, Electron Microscopy, Derivative Assay, Western Blot, Comparison, Saline, Silver Staining, Single Particle, Imaging, Raman Spectroscopy, Molecular Weight, Marker

    Encapsulation efficiency evaluation and comparison between electroporation and sodium carbonate treatment. A Spectrofluorometer analysis for quantification of Dextran-FITC incorporation after 50 V electroporation (see material and methods) or sodium carbonate treatment of HEK293-derived nsEVs (25 µg/ml) in various nsEVs:Dextran-FITC ratios (1:1, 1:1.5 and 1:2). B Confocal microscopy images of Hela cells treated for 24 h with Dextran-FITC bearing nsEVs (25 µg/ml) after electroporation (50 V) or sodium carbonate incubation in NsEVs:Dextran-FITC = 1:1.5 molecular ratio (blue = DAPI; green = Dextran-FITC bearing nsEVs). C Spectrofluorometer analysis for quantification of SAP-FITC incorporation after 50 V electroporation (see material and methods) or sodium carbonate treatment of HEK293-derived nsEVs (25 µg/ml) in nsEVs:SAP-FITC = 1:1.5 ratio

    Journal: Discover Nano

    Article Title: Novel loading protocol combines highly efficient encapsulation of exogenous therapeutic toxin with preservation of extracellular vesicles properties, uptake and cargo activity

    doi: 10.1186/s11671-024-04022-8

    Figure Lengend Snippet: Encapsulation efficiency evaluation and comparison between electroporation and sodium carbonate treatment. A Spectrofluorometer analysis for quantification of Dextran-FITC incorporation after 50 V electroporation (see material and methods) or sodium carbonate treatment of HEK293-derived nsEVs (25 µg/ml) in various nsEVs:Dextran-FITC ratios (1:1, 1:1.5 and 1:2). B Confocal microscopy images of Hela cells treated for 24 h with Dextran-FITC bearing nsEVs (25 µg/ml) after electroporation (50 V) or sodium carbonate incubation in NsEVs:Dextran-FITC = 1:1.5 molecular ratio (blue = DAPI; green = Dextran-FITC bearing nsEVs). C Spectrofluorometer analysis for quantification of SAP-FITC incorporation after 50 V electroporation (see material and methods) or sodium carbonate treatment of HEK293-derived nsEVs (25 µg/ml) in nsEVs:SAP-FITC = 1:1.5 ratio

    Article Snippet: HEK293 (human embryonic kidney-derived) cells were purchased from ATCC.

    Techniques: Encapsulation, Comparison, Electroporation, Derivative Assay, Confocal Microscopy, Incubation

    Evaluation of sodium carbonate-treated SAP-bearing nsEVs uptake. A Bright field (upper row) and fluorescent (lower row) microscopy images of 5637 cells 24 h after incubation with HEK293-derived nsEVs treated with phosphate buffer saline (PBS, left) or sodium carbonate (Na 2 CO 3 , right) in the presence of SAP and stained with Vybrant Dio lipophilic dye. Different concentrations of nsEVs (5 and 10 µg) were used for comparison. Representative images of three independent experiments. B Flow cytometry analysis of 5637 cells 24 h after treatment with 5 or 10 µg of PBS or Na 2 CO 3 -treated SAP-bearing nsEVs. Results are shown as mean fluorescence percentage + SD from 3 independent experiments

    Journal: Discover Nano

    Article Title: Novel loading protocol combines highly efficient encapsulation of exogenous therapeutic toxin with preservation of extracellular vesicles properties, uptake and cargo activity

    doi: 10.1186/s11671-024-04022-8

    Figure Lengend Snippet: Evaluation of sodium carbonate-treated SAP-bearing nsEVs uptake. A Bright field (upper row) and fluorescent (lower row) microscopy images of 5637 cells 24 h after incubation with HEK293-derived nsEVs treated with phosphate buffer saline (PBS, left) or sodium carbonate (Na 2 CO 3 , right) in the presence of SAP and stained with Vybrant Dio lipophilic dye. Different concentrations of nsEVs (5 and 10 µg) were used for comparison. Representative images of three independent experiments. B Flow cytometry analysis of 5637 cells 24 h after treatment with 5 or 10 µg of PBS or Na 2 CO 3 -treated SAP-bearing nsEVs. Results are shown as mean fluorescence percentage + SD from 3 independent experiments

    Article Snippet: HEK293 (human embryonic kidney-derived) cells were purchased from ATCC.

    Techniques: Microscopy, Incubation, Derivative Assay, Saline, Staining, Comparison, Flow Cytometry, Fluorescence

    Figure 10 SLIT3-loaded and SLIT3-free scaffold cell population after different time period at three cell densities.

    Journal: Journal of Materials Science

    Article Title: A hierarchically porous and SLIT3-releasing scaffold for bone tissue engineering applications

    doi: 10.1007/s10853-024-10379-z

    Figure Lengend Snippet: Figure 10 SLIT3-loaded and SLIT3-free scaffold cell population after different time period at three cell densities.

    Article Snippet: Human embryonic kidney cell (HEK293)-derived SLIT3 recombinant protein with C-terminal 6-his-tag and a predicted molecular mass of 45 kDa was purchased from R&D systems, USA.

    Techniques:

    Journal: Cell Reports Medicine

    Article Title: A diverse collection of B cells responded to HIV infection in infant BG505

    doi: 10.1016/j.xcrm.2021.100314

    Figure Lengend Snippet:

    Article Snippet: For antibody production: HEK293-F cells (RRID:CVCL_D603; originally derived from female human embryonic kidney cells) were obtained from Invitrogen (Thermo Fisher Scientific, Waltham, MA, catalog #R790-07) and grown at 37°C in Freestyle 293 Expression Medium (Thermo Fisher Scientific, catalog #12338002) in baffle-bottomed flasks orbiting at 135 rpm.

    Techniques: Clone Assay, Recombinant, Expressing, Sequencing, Amplification, Plasmid Preparation, Software