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sxfm imaging pc12 cells  (ATCC)


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    ATCC sxfm imaging pc12 cells
    Contour plots of Pu Lα X-ray fluorescence intensity measured by <t>SXFM</t> superimposed on optical images of cells. (a) Pu-free control cell; (b) uptake of Pu as PuCFeNTf; (c) very low uptake of mixed FeCPuNTf and of (d) chloroquine-treated cells exposed to PuCFeNTf. The Pu observed on the left edge of panel d is associated with cellular debris. The average background corrected Pu content (e) of the Pu-containing cells exposed to closed PuCFeNTf (labeled “PuCFeNTf”, n = 8) is greater than that of control cells (labeled “Control”, n = 20), cells simultaneously treated with 50 μM chloroquine and PuCFeNTf (labeled “Chloroquine”, n = 8), cells exposed to FeCPuNTf (labeled “FeCPuNTf”, n = 21), or cells exposed to an equimolar mixture of Fe2Tf and PuCFeNTf (labeled “Fe2Tf”, n = 4). The error bars are ±S.E.M. at 95% confidence.
    Sxfm Imaging Pc12 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 4408 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sxfm+imaging+pc12+cells/PC-12/pmc03462652-216-3-7
    Average 98 stars, based on 4408 article reviews
    sxfm imaging pc12 cells - by Bioz Stars, 2026-09
    98/100 stars

    Images

    1) Product Images from "An iron-dependent and transferrin-mediated cellular uptake pathway for plutonium"

    Article Title: An iron-dependent and transferrin-mediated cellular uptake pathway for plutonium

    Journal: Nature chemical biology

    doi: 10.1038/nchembio.594

    Contour plots of Pu Lα X-ray fluorescence intensity measured by SXFM superimposed on optical images of cells. (a) Pu-free control cell; (b) uptake of Pu as PuCFeNTf; (c) very low uptake of mixed FeCPuNTf and of (d) chloroquine-treated cells exposed to PuCFeNTf. The Pu observed on the left edge of panel d is associated with cellular debris. The average background corrected Pu content (e) of the Pu-containing cells exposed to closed PuCFeNTf (labeled “PuCFeNTf”, n = 8) is greater than that of control cells (labeled “Control”, n = 20), cells simultaneously treated with 50 μM chloroquine and PuCFeNTf (labeled “Chloroquine”, n = 8), cells exposed to FeCPuNTf (labeled “FeCPuNTf”, n = 21), or cells exposed to an equimolar mixture of Fe2Tf and PuCFeNTf (labeled “Fe2Tf”, n = 4). The error bars are ±S.E.M. at 95% confidence.
    Figure Legend Snippet: Contour plots of Pu Lα X-ray fluorescence intensity measured by SXFM superimposed on optical images of cells. (a) Pu-free control cell; (b) uptake of Pu as PuCFeNTf; (c) very low uptake of mixed FeCPuNTf and of (d) chloroquine-treated cells exposed to PuCFeNTf. The Pu observed on the left edge of panel d is associated with cellular debris. The average background corrected Pu content (e) of the Pu-containing cells exposed to closed PuCFeNTf (labeled “PuCFeNTf”, n = 8) is greater than that of control cells (labeled “Control”, n = 20), cells simultaneously treated with 50 μM chloroquine and PuCFeNTf (labeled “Chloroquine”, n = 8), cells exposed to FeCPuNTf (labeled “FeCPuNTf”, n = 21), or cells exposed to an equimolar mixture of Fe2Tf and PuCFeNTf (labeled “Fe2Tf”, n = 4). The error bars are ±S.E.M. at 95% confidence.

    Techniques Used: Fluorescence, Control, Labeling

    Related Articles

    Imaging:

    Article Title: An iron-dependent and transferrin-mediated cellular uptake pathway for plutonium
    Article Snippet: Cell Uptake and SXFM Imaging PC12 cells (ATCC) were grown in F12K medium supplemented with 12.5 % horse serum, 2.5% fetal calf serum, and antibiotics in humidified 5% CO 2 at 37°C. .. Cell Uptake and SXFM Imaging PC12 cells (ATCC) were grown in F12K medium supplemented with 12.5 % horse serum, 2.5% fetal calf serum, and antibiotics in humidified 5% CO 2 at 37°C. ..



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    sxfm imaging pc12 cells  (ATCC)
    98
    ATCC sxfm imaging pc12 cells
    Contour plots of Pu Lα X-ray fluorescence intensity measured by <t>SXFM</t> superimposed on optical images of cells. (a) Pu-free control cell; (b) uptake of Pu as PuCFeNTf; (c) very low uptake of mixed FeCPuNTf and of (d) chloroquine-treated cells exposed to PuCFeNTf. The Pu observed on the left edge of panel d is associated with cellular debris. The average background corrected Pu content (e) of the Pu-containing cells exposed to closed PuCFeNTf (labeled “PuCFeNTf”, n = 8) is greater than that of control cells (labeled “Control”, n = 20), cells simultaneously treated with 50 μM chloroquine and PuCFeNTf (labeled “Chloroquine”, n = 8), cells exposed to FeCPuNTf (labeled “FeCPuNTf”, n = 21), or cells exposed to an equimolar mixture of Fe2Tf and PuCFeNTf (labeled “Fe2Tf”, n = 4). The error bars are ±S.E.M. at 95% confidence.
    Sxfm Imaging Pc12 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sxfm+imaging+pc12+cells/PC-12/pmc03462652-216-3-7
    Average 98 stars, based on 1 article reviews
    sxfm imaging pc12 cells - by Bioz Stars, 2026-09
    98/100 stars
    		  Buy from Supplier

    Image Search Results


    Contour plots of Pu Lα X-ray fluorescence intensity measured by SXFM superimposed on optical images of cells. (a) Pu-free control cell; (b) uptake of Pu as PuCFeNTf; (c) very low uptake of mixed FeCPuNTf and of (d) chloroquine-treated cells exposed to PuCFeNTf. The Pu observed on the left edge of panel d is associated with cellular debris. The average background corrected Pu content (e) of the Pu-containing cells exposed to closed PuCFeNTf (labeled “PuCFeNTf”, n = 8) is greater than that of control cells (labeled “Control”, n = 20), cells simultaneously treated with 50 μM chloroquine and PuCFeNTf (labeled “Chloroquine”, n = 8), cells exposed to FeCPuNTf (labeled “FeCPuNTf”, n = 21), or cells exposed to an equimolar mixture of Fe2Tf and PuCFeNTf (labeled “Fe2Tf”, n = 4). The error bars are ±S.E.M. at 95% confidence.

    Journal: Nature chemical biology

    Article Title: An iron-dependent and transferrin-mediated cellular uptake pathway for plutonium

    doi: 10.1038/nchembio.594

    Figure Lengend Snippet: Contour plots of Pu Lα X-ray fluorescence intensity measured by SXFM superimposed on optical images of cells. (a) Pu-free control cell; (b) uptake of Pu as PuCFeNTf; (c) very low uptake of mixed FeCPuNTf and of (d) chloroquine-treated cells exposed to PuCFeNTf. The Pu observed on the left edge of panel d is associated with cellular debris. The average background corrected Pu content (e) of the Pu-containing cells exposed to closed PuCFeNTf (labeled “PuCFeNTf”, n = 8) is greater than that of control cells (labeled “Control”, n = 20), cells simultaneously treated with 50 μM chloroquine and PuCFeNTf (labeled “Chloroquine”, n = 8), cells exposed to FeCPuNTf (labeled “FeCPuNTf”, n = 21), or cells exposed to an equimolar mixture of Fe2Tf and PuCFeNTf (labeled “Fe2Tf”, n = 4). The error bars are ±S.E.M. at 95% confidence.

    Article Snippet: Cell Uptake and SXFM Imaging PC12 cells (ATCC) were grown in F12K medium supplemented with 12.5 % horse serum, 2.5% fetal calf serum, and antibiotics in humidified 5% CO 2 at 37°C.

    Techniques: Fluorescence, Control, Labeling