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plain polystyrene microspheres ps  (Chrom Tech)

 
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    Chrom Tech plain polystyrene microspheres ps
    Plain Polystyrene Microspheres Ps, supplied by Chrom Tech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/plain+polystyrene+microspheres+ps/microspheres+monodisperse+polystyrene/pm41865576-50-5-21
    Average 86 stars, based on 1 article reviews
    plain polystyrene microspheres ps - by Bioz Stars, 2026-10
    86/100 stars

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    Related Articles

    other:

    Article Title: Co-exposure to polystyrene microplastics and glyphosate induces gut microbiota dysbiosis and cognitive impairment in honeybees.
    Article Snippet: • PS and GLY co-exposure showed more severe impacts on honeybee survival



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    Confocal microscopy images of [A(1)] untreated HEK293 culture and [B(1–3),C(1–3)] 1 <t>μm</t> <t>green-fluorescent</t> polystyrene microplastic particle-treated cultures. HEK 293 kidney cells were exposed to 5 μg/mL 1 μm green-fluorescent <t>PS-MPs</t> for 72 h before fixation. Then, the HEK 293 cells were stained with a wheat germ agglutinin 594 conjugate plasma membrane stain (red) and a nuclear stain DAPI (blue). Panels [A(1)–C(1)] are top-down composites of images in a Z-stack. The internalization of the microplastic is shown in the ortho YZ plane {the green box at the right edge of [A(1),B(1),C(1)]} and the XZ plane {the yellow box at the bottom of [A(1),B(1),C(1)]}. The white arrows indicate microplastic particles inside the cells. White axes from the particle of interest are drawn to the XZ and YZ panels on the sides and point out the dimension of the cell that is seen in the top-down view. Panels [B(2),C(2)] show 3-D top view angles of [B(1),C(1)] images, respectively. Panels [B(3),C(3)] show the 3-D side view angles of [B(1),C(1)] images, respectively. These images were taken at 1000× magnification. Scale bar: 10 μm.
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    Image Search Results


    Confocal microscopy images of [A(1)] untreated HEK293 culture and [B(1–3),C(1–3)] 1 μm green-fluorescent polystyrene microplastic particle-treated cultures. HEK 293 kidney cells were exposed to 5 μg/mL 1 μm green-fluorescent PS-MPs for 72 h before fixation. Then, the HEK 293 cells were stained with a wheat germ agglutinin 594 conjugate plasma membrane stain (red) and a nuclear stain DAPI (blue). Panels [A(1)–C(1)] are top-down composites of images in a Z-stack. The internalization of the microplastic is shown in the ortho YZ plane {the green box at the right edge of [A(1),B(1),C(1)]} and the XZ plane {the yellow box at the bottom of [A(1),B(1),C(1)]}. The white arrows indicate microplastic particles inside the cells. White axes from the particle of interest are drawn to the XZ and YZ panels on the sides and point out the dimension of the cell that is seen in the top-down view. Panels [B(2),C(2)] show 3-D top view angles of [B(1),C(1)] images, respectively. Panels [B(3),C(3)] show the 3-D side view angles of [B(1),C(1)] images, respectively. These images were taken at 1000× magnification. Scale bar: 10 μm.

    Journal: ACS Omega

    Article Title: Effects of Polystyrene Microplastics on Human Kidney and Liver Cell Morphology, Cellular Proliferation, and Metabolism

    doi: 10.1021/acsomega.2c03453

    Figure Lengend Snippet: Confocal microscopy images of [A(1)] untreated HEK293 culture and [B(1–3),C(1–3)] 1 μm green-fluorescent polystyrene microplastic particle-treated cultures. HEK 293 kidney cells were exposed to 5 μg/mL 1 μm green-fluorescent PS-MPs for 72 h before fixation. Then, the HEK 293 cells were stained with a wheat germ agglutinin 594 conjugate plasma membrane stain (red) and a nuclear stain DAPI (blue). Panels [A(1)–C(1)] are top-down composites of images in a Z-stack. The internalization of the microplastic is shown in the ortho YZ plane {the green box at the right edge of [A(1),B(1),C(1)]} and the XZ plane {the yellow box at the bottom of [A(1),B(1),C(1)]}. The white arrows indicate microplastic particles inside the cells. White axes from the particle of interest are drawn to the XZ and YZ panels on the sides and point out the dimension of the cell that is seen in the top-down view. Panels [B(2),C(2)] show 3-D top view angles of [B(1),C(1)] images, respectively. Panels [B(3),C(3)] show the 3-D side view angles of [B(1),C(1)] images, respectively. These images were taken at 1000× magnification. Scale bar: 10 μm.

    Article Snippet: The plain and the green-fluorescent polystyrene microspheres (PS-MPs) of size 1 μm were purchased from Degradex (Phosphorex).

    Techniques: Confocal Microscopy, Staining

    Confocal microscopy images of [A(1)] untreated Hep G2 culture and [B(1–3),C(1–3)] 1 μm green-fluorescent polystyrene microplastic particle-treated cultures. The internalization of the 1 μm microplastics can be visualized in Z -axis stacks. Hep G2 cells were exposed to 5 μg/mL 1 μm green-fluorescent PS-MPs for 72 h before fixation. Then, the cells were stained with a wheat germ agglutinin 594 conjugate plasma membrane stain (shown in red) and a nuclear stain DAPI (shown in blue). Panels [A(1)–C(1)] are top-down composites of images in a Z-stack. Internalization of the microplastic is shown in the ortho YZ plane {the green-boxed edge right panel of [A(1),B(1),C(1)]} and the XZ plane {the yellow-boxed bottom panel of [A(1),B(1),C(1)]}. The white arrows indicate microplastic particles inside the cells. White axes from the particle of interest are drawn to the XZ and YZ panels on the sides and point out the dimension of the cell that is seen in the top-down view. Panels [B(2),C(2)] show 3-D top view angles of [B(1),C(1)] images, respectively. Panels [B(3),C(3)] show the 3-D side view angles of [B(1),C(1)] images, respectively. These images were taken at 1000× magnification. Scale bar: 10 μm.

    Journal: ACS Omega

    Article Title: Effects of Polystyrene Microplastics on Human Kidney and Liver Cell Morphology, Cellular Proliferation, and Metabolism

    doi: 10.1021/acsomega.2c03453

    Figure Lengend Snippet: Confocal microscopy images of [A(1)] untreated Hep G2 culture and [B(1–3),C(1–3)] 1 μm green-fluorescent polystyrene microplastic particle-treated cultures. The internalization of the 1 μm microplastics can be visualized in Z -axis stacks. Hep G2 cells were exposed to 5 μg/mL 1 μm green-fluorescent PS-MPs for 72 h before fixation. Then, the cells were stained with a wheat germ agglutinin 594 conjugate plasma membrane stain (shown in red) and a nuclear stain DAPI (shown in blue). Panels [A(1)–C(1)] are top-down composites of images in a Z-stack. Internalization of the microplastic is shown in the ortho YZ plane {the green-boxed edge right panel of [A(1),B(1),C(1)]} and the XZ plane {the yellow-boxed bottom panel of [A(1),B(1),C(1)]}. The white arrows indicate microplastic particles inside the cells. White axes from the particle of interest are drawn to the XZ and YZ panels on the sides and point out the dimension of the cell that is seen in the top-down view. Panels [B(2),C(2)] show 3-D top view angles of [B(1),C(1)] images, respectively. Panels [B(3),C(3)] show the 3-D side view angles of [B(1),C(1)] images, respectively. These images were taken at 1000× magnification. Scale bar: 10 μm.

    Article Snippet: The plain and the green-fluorescent polystyrene microspheres (PS-MPs) of size 1 μm were purchased from Degradex (Phosphorex).

    Techniques: Confocal Microscopy, Staining