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adhesive hek 293 cell line  (ATCC)


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    Structured Review

    ATCC adhesive hek 293 cell line
    Adhesive Hek 293 Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 22376 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hek+293+cell+line/293/us12649908-446-17-23
    Average 99 stars, based on 22376 article reviews
    adhesive hek 293 cell line - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Single-cell activation screen identifies hepatic maturation regulators with zonal resolution.
    Article Snippet: The media was refreshed every day, and the cells were passaged every other day with TrypLE (Thermo, 12604-021). .. The HEK-293 cell line (ATCC, CRL-1573) was cultured in KnockOut DMEM (Thermo, 10829018), 10% fetal bovine serum (PAN biotech, P30-2602), 100 U/ml penicillin, 100 μg/ml streptomycin (Gibco, 15140148), 1X MEM Non-Essential Amino Acids Solution (Gibco, 11140035), 4 mM GlutaMAX (Gibco, 35050-038), 55 μM b-mercaptoethanol (Thermo, 21985023) at 37 ◦ C with 5% CO 2 in a humidified incubator. ..

    Knock-Out:

    Article Title: Single-cell activation screen identifies hepatic maturation regulators with zonal resolution.
    Article Snippet: The media was refreshed every day, and the cells were passaged every other day with TrypLE (Thermo, 12604-021). .. The HEK-293 cell line (ATCC, CRL-1573) was cultured in KnockOut DMEM (Thermo, 10829018), 10% fetal bovine serum (PAN biotech, P30-2602), 100 U/ml penicillin, 100 μg/ml streptomycin (Gibco, 15140148), 1X MEM Non-Essential Amino Acids Solution (Gibco, 11140035), 4 mM GlutaMAX (Gibco, 35050-038), 55 μM b-mercaptoethanol (Thermo, 21985023) at 37 ◦ C with 5% CO 2 in a humidified incubator. ..

    Concentration Assay:

    Article Title: Optimized ND4 allotopic expression for gene therapy of Leber’s hereditary optic neuropathy
    Article Snippet: .. The HEK-293 cell line (ATCC cat. CRL-1573) was transferred to DMEM medium containing 4.5 g/L glucose (Biosera cat. PM-D1115), 5% v/v FBS (Biowest, cat. S1600), 2.5 mM pyruvate (PanEco, cat. F023), 1× NEAA (PanEco, cat. F115), 100 μg/mL uridine (Sigma-Aldrich, cat. U3750), and 25 ng/mL EtBr (Sigma-Aldrich, cat. 46067) with a monthly increase in concentration to 50, 100, 200, 300, and finally 400 ng/mL ( ). ..

    Modification:

    Article Title: Characterization of Novel Variants in P2YRY12, GP6 and TBXAS1 in Patients with Lifelong History of Bleeding
    Article Snippet: Transient expression experiments were performed using pcDNA3.1+/C-(K)-DYK with complementary DNA (cDNA) wild-type of P2RY12 , TBXAS1 and GP6 , or mutants, all of them available commercially (OHu14933D, GenScript, Rijswijk, The Netherlands). .. HEK 293 cell line (ATCC, LGC Standards S.L.U, Barcelona, Spain) was grown in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% of fetal bovine serum (FBS). .. Transient expression assays were performed by plating 7 × 10 4 cells/well and adding all 2 μg/well of all plasmids using Lipofectamine 3000 kit (Thermo Fisher Scientific).

    Diagnostic Assay:

    Article Title: Isolation, characterization and testing of RNA aptamers targeting glutamate receptors in a rat spinal cord injury pain model
    Article Snippet: Clinical trial registration Study protocol Data collection Outcomes Dual use research of concern Policy information about dual use research of concern Hazards Could the accidental, deliberate or reckless misuse of agents or technologies generated in the work, or the application of information presented in the manuscript, pose a threat to: Sprague Dawley males, females yes All animal procedures followed NIH guidelines and were approved by the University of Miami Institutional Animal Care and Use Committee. .. HEK-293 cell line The cell line was purchased from ATCC, which was authenticated, contaminant-free No N/A N/A N/A N/A N/A N/A N/A N/A for this section No Yes Public health National security Crops and/or livestock Ecosystems Any other significant area Experiments of concern Does the work involve any of these experiments of concern: No Yes Demonstrate how to render a vaccine ineffective Confer resistance to therapeutically useful antibiotics or antiviral agents Enhance the virulence of a pathogen or render a nonpathogen virulent Increase transmissibility of a pathogen Alter the host range of a pathogen Enable evasion of diagnostic/detection modalities Enable the weaponization of a biological agent or toxin Any other potentially harmful combination of experiments and agents Novel plant genotypes Seed stocks Authentication Plants ChIP-seq Data deposition Confirm that both raw and final processed data have been deposited in a public database such as GEO. ..

    Chromatin Immunoprecipitation:

    Article Title: Isolation, characterization and testing of RNA aptamers targeting glutamate receptors in a rat spinal cord injury pain model
    Article Snippet: Clinical trial registration Study protocol Data collection Outcomes Dual use research of concern Policy information about dual use research of concern Hazards Could the accidental, deliberate or reckless misuse of agents or technologies generated in the work, or the application of information presented in the manuscript, pose a threat to: Sprague Dawley males, females yes All animal procedures followed NIH guidelines and were approved by the University of Miami Institutional Animal Care and Use Committee. .. HEK-293 cell line The cell line was purchased from ATCC, which was authenticated, contaminant-free No N/A N/A N/A N/A N/A N/A N/A N/A for this section No Yes Public health National security Crops and/or livestock Ecosystems Any other significant area Experiments of concern Does the work involve any of these experiments of concern: No Yes Demonstrate how to render a vaccine ineffective Confer resistance to therapeutically useful antibiotics or antiviral agents Enhance the virulence of a pathogen or render a nonpathogen virulent Increase transmissibility of a pathogen Alter the host range of a pathogen Enable evasion of diagnostic/detection modalities Enable the weaponization of a biological agent or toxin Any other potentially harmful combination of experiments and agents Novel plant genotypes Seed stocks Authentication Plants ChIP-seq Data deposition Confirm that both raw and final processed data have been deposited in a public database such as GEO. ..



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    ATCC hek cell line
    a , Differential spectra between 50 Chol-enriched and unenriched <t>HEK</t> cells. Data are presented as mean values ± s.d. For comparison, MβCD–Chol complex spectrum acquired with ATR–FTIR spectroscopy is shown in black. Chol-enriched HEK cells showed a peak at 1,048 cm −1 , corresponding to the absorption peak of the MβCD–Chol complex. b , Violin plots showing the kernel density of the AUC of the peak at 1,048 cm −1 before (T0) and 16 h (T16) after exposure to the MβCD–Chol complex. Box plot minima and maxima inside the violin plots indicate the interquartile range, the white circles indicate the mean values and the whiskers indicate the s.d. (coefficient of 1). Outliers are shown as individual points. *** P = 1.46 × 10 −28 from a two-sided paired t -test. N = 3. c , HyFOPM micrographs of HEK cells before (T0) and after treatment (T16) with MβCD–Chol complexes. Overlay maps are obtained from Chol (1,048 cm −1 ) and SM contrast (1,464 cm −1 ). d , e , Box plots representing the OptA contrast of the micrographs in c : the Chol contrast (1,048 cm −1 ) ( d ) and the SM contrast (1,464 cm −1 ) ( e ) for MβCD-treated HEK cells at time 0 h (T0) and 16 h (T16). Box plots indicate the s.e.m. (coefficient of 1; box limits), the white circles indicate the mean values, while the centered lines the median values, and the whiskers indicate the s.d. (coefficient of 1). Outliers are shown as individual points. *** P = 6.19 × 10 −12 ( d ) and P = 5.48 × 10 −8 ( e ) from a two-sided paired t -test. Scale bar, 300 μm, N = 3. OptA, optoacoustic; NOptA, normalized optoacoustic.
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    Image Search Results


    a , Differential spectra between 50 Chol-enriched and unenriched HEK cells. Data are presented as mean values ± s.d. For comparison, MβCD–Chol complex spectrum acquired with ATR–FTIR spectroscopy is shown in black. Chol-enriched HEK cells showed a peak at 1,048 cm −1 , corresponding to the absorption peak of the MβCD–Chol complex. b , Violin plots showing the kernel density of the AUC of the peak at 1,048 cm −1 before (T0) and 16 h (T16) after exposure to the MβCD–Chol complex. Box plot minima and maxima inside the violin plots indicate the interquartile range, the white circles indicate the mean values and the whiskers indicate the s.d. (coefficient of 1). Outliers are shown as individual points. *** P = 1.46 × 10 −28 from a two-sided paired t -test. N = 3. c , HyFOPM micrographs of HEK cells before (T0) and after treatment (T16) with MβCD–Chol complexes. Overlay maps are obtained from Chol (1,048 cm −1 ) and SM contrast (1,464 cm −1 ). d , e , Box plots representing the OptA contrast of the micrographs in c : the Chol contrast (1,048 cm −1 ) ( d ) and the SM contrast (1,464 cm −1 ) ( e ) for MβCD-treated HEK cells at time 0 h (T0) and 16 h (T16). Box plots indicate the s.e.m. (coefficient of 1; box limits), the white circles indicate the mean values, while the centered lines the median values, and the whiskers indicate the s.d. (coefficient of 1). Outliers are shown as individual points. *** P = 6.19 × 10 −12 ( d ) and P = 5.48 × 10 −8 ( e ) from a two-sided paired t -test. Scale bar, 300 μm, N = 3. OptA, optoacoustic; NOptA, normalized optoacoustic.

    Journal: Nature Methods

    Article Title: Differentiation of sphingomyelin and cholesterol by hyperspectral mid-infrared detection of single-bond vibrational modes in the fingerprint region

    doi: 10.1038/s41592-026-03025-w

    Figure Lengend Snippet: a , Differential spectra between 50 Chol-enriched and unenriched HEK cells. Data are presented as mean values ± s.d. For comparison, MβCD–Chol complex spectrum acquired with ATR–FTIR spectroscopy is shown in black. Chol-enriched HEK cells showed a peak at 1,048 cm −1 , corresponding to the absorption peak of the MβCD–Chol complex. b , Violin plots showing the kernel density of the AUC of the peak at 1,048 cm −1 before (T0) and 16 h (T16) after exposure to the MβCD–Chol complex. Box plot minima and maxima inside the violin plots indicate the interquartile range, the white circles indicate the mean values and the whiskers indicate the s.d. (coefficient of 1). Outliers are shown as individual points. *** P = 1.46 × 10 −28 from a two-sided paired t -test. N = 3. c , HyFOPM micrographs of HEK cells before (T0) and after treatment (T16) with MβCD–Chol complexes. Overlay maps are obtained from Chol (1,048 cm −1 ) and SM contrast (1,464 cm −1 ). d , e , Box plots representing the OptA contrast of the micrographs in c : the Chol contrast (1,048 cm −1 ) ( d ) and the SM contrast (1,464 cm −1 ) ( e ) for MβCD-treated HEK cells at time 0 h (T0) and 16 h (T16). Box plots indicate the s.e.m. (coefficient of 1; box limits), the white circles indicate the mean values, while the centered lines the median values, and the whiskers indicate the s.d. (coefficient of 1). Outliers are shown as individual points. *** P = 6.19 × 10 −12 ( d ) and P = 5.48 × 10 −8 ( e ) from a two-sided paired t -test. Scale bar, 300 μm, N = 3. OptA, optoacoustic; NOptA, normalized optoacoustic.

    Article Snippet: Accumulation of SM and Chol was performed respectively on a human adenocarcinoma alveolar basal epithelial cell line (A549, American Type Culture Collection (ATCC): CCL-185) and a HEK cell line (HEK293, ATCC: CRL-1573).

    Techniques: Comparison, Spectroscopy

    a) Comparison between the hyperspectral fingerprint optoacoustic microscopy (hyFOPM)’s spectra of a Chol liquid solution (green line) and of MβCD - Chol complex (purple line). The Chol absorption peak shifts from 1056 cm −1 to 1048 cm −1 when Chol is complexed with cyclodextrins. b) Comparison between the Fourier transform infrared (FTIR) spectra of MβCD complex with Chol (in red) and MβCD without Chol (in blue). For comparison, the FTIR spectrum of a Chol liquid solution is plotted in black. c) HyFOPM images monitoring Chol loading in HEK cells at 1375 cm −1 (Chol contrast), at 1540 cm −1 (protein contrast), and at 2852 cm −1 (lipid contrast) before (T0) and after 16 hours (T16) of treatment with MβCD-Chol. Boxplots representing the optoacoustic contrast of HEK cells in (c) at (d) 1375 cm −1 (Chol contrast), at (e) 2852 cm −1 (lipid contrast) and at (f) 1540 cm −1 (protein contrast). Box plots indicate the standard error (SE, coefficient =1; box limits), the white circles indicate the mean values, while the centered lines the median values, and the whiskers indicate the standard deviation (SD, coefficient =1). Outliers are shown as individual points. ***p = 2.24 × 10 −28 ( d ), p = 3.16 × 10 −8 ( e ) and p = 0.0018 ( f ) from a two-sided paired t-test. N = 3. OptA: Optoacoustic; NOptA: Normalized Optoacoustic.

    Journal: Nature Methods

    Article Title: Differentiation of sphingomyelin and cholesterol by hyperspectral mid-infrared detection of single-bond vibrational modes in the fingerprint region

    doi: 10.1038/s41592-026-03025-w

    Figure Lengend Snippet: a) Comparison between the hyperspectral fingerprint optoacoustic microscopy (hyFOPM)’s spectra of a Chol liquid solution (green line) and of MβCD - Chol complex (purple line). The Chol absorption peak shifts from 1056 cm −1 to 1048 cm −1 when Chol is complexed with cyclodextrins. b) Comparison between the Fourier transform infrared (FTIR) spectra of MβCD complex with Chol (in red) and MβCD without Chol (in blue). For comparison, the FTIR spectrum of a Chol liquid solution is plotted in black. c) HyFOPM images monitoring Chol loading in HEK cells at 1375 cm −1 (Chol contrast), at 1540 cm −1 (protein contrast), and at 2852 cm −1 (lipid contrast) before (T0) and after 16 hours (T16) of treatment with MβCD-Chol. Boxplots representing the optoacoustic contrast of HEK cells in (c) at (d) 1375 cm −1 (Chol contrast), at (e) 2852 cm −1 (lipid contrast) and at (f) 1540 cm −1 (protein contrast). Box plots indicate the standard error (SE, coefficient =1; box limits), the white circles indicate the mean values, while the centered lines the median values, and the whiskers indicate the standard deviation (SD, coefficient =1). Outliers are shown as individual points. ***p = 2.24 × 10 −28 ( d ), p = 3.16 × 10 −8 ( e ) and p = 0.0018 ( f ) from a two-sided paired t-test. N = 3. OptA: Optoacoustic; NOptA: Normalized Optoacoustic.

    Article Snippet: Accumulation of SM and Chol was performed respectively on a human adenocarcinoma alveolar basal epithelial cell line (A549, American Type Culture Collection (ATCC): CCL-185) and a HEK cell line (HEK293, ATCC: CRL-1573).

    Techniques: Comparison, Microscopy, Fourier Transform Infrared Spectroscopy, Standard Deviation