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matrigel-coated transwell chambers  (Corning Life Sciences)

 
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    Corning Life Sciences matrigel-coated transwell chambers
    Matrigel Coated Transwell Chambers, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/matrigel-coated transwell chambers/product/Corning Life Sciences
    Average 90 stars, based on 1 article reviews
    matrigel-coated transwell chambers - by Bioz Stars, 2026-03
    90/100 stars

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    Cellular uptake of Squ@APS NPs and Squ@APS-IR820 NPs and <t>transwell</t> invasion assays. Fluorescence image of 4T1 cells co-cultured with Squ/C6@APS (A) and Squ/C6@APS-IR820 (B) at 1 h, 3 h, and 6 h, respectively. Blue and green represent DAPI and C6 fluorescence, which stand for the position of cell nucleus and NPs. The endocytosis of Squ/C6@APS (C) and Squ/C6@APS-IR820 (D) by 4T1 cells was visualized by flow cytometry. Blank represents cells treated with the same volume of medium, which was used as a control (Red). The mean fluorescence intensity (MFI) value (E) of 4T1 cells co-cultured with Squ/C6@APS and Squ/C6@APS-IR820NPs for 1 h, 3 h, and 6 h. Fluorescence image (F) and the mean fluorescence intensity (MFI) value (G) of 4T1 cells co-cultured with Squ/C6@APS-IR820 NPs for 3 h pretreated with 100 μM of probenecid or 50 μM of doxorubicin for 30 min. Invasion of 4T1 cells treated with saline (H), Squ@APS-IR820 NPs (I), MnO 2 @APS-IR820 (J), and Squ@APS-IR820 NPs + MnO 2 @APS-IR820 (K). Invasive cells in every field (L). Data are presented as means ± standard deviation (SD). Differences among groups were evaluated by one-way ANOVA analysis. ∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05. ns, no significant difference. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    Cellular uptake of Squ@APS NPs and Squ@APS-IR820 NPs and <t>transwell</t> invasion assays. Fluorescence image of 4T1 cells co-cultured with Squ/C6@APS (A) and Squ/C6@APS-IR820 (B) at 1 h, 3 h, and 6 h, respectively. Blue and green represent DAPI and C6 fluorescence, which stand for the position of cell nucleus and NPs. The endocytosis of Squ/C6@APS (C) and Squ/C6@APS-IR820 (D) by 4T1 cells was visualized by flow cytometry. Blank represents cells treated with the same volume of medium, which was used as a control (Red). The mean fluorescence intensity (MFI) value (E) of 4T1 cells co-cultured with Squ/C6@APS and Squ/C6@APS-IR820NPs for 1 h, 3 h, and 6 h. Fluorescence image (F) and the mean fluorescence intensity (MFI) value (G) of 4T1 cells co-cultured with Squ/C6@APS-IR820 NPs for 3 h pretreated with 100 μM of probenecid or 50 μM of doxorubicin for 30 min. Invasion of 4T1 cells treated with saline (H), Squ@APS-IR820 NPs (I), MnO 2 @APS-IR820 (J), and Squ@APS-IR820 NPs + MnO 2 @APS-IR820 (K). Invasive cells in every field (L). Data are presented as means ± standard deviation (SD). Differences among groups were evaluated by one-way ANOVA analysis. ∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05. ns, no significant difference. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    Cellular uptake of Squ@APS NPs and Squ@APS-IR820 NPs and <t>transwell</t> invasion assays. Fluorescence image of 4T1 cells co-cultured with Squ/C6@APS (A) and Squ/C6@APS-IR820 (B) at 1 h, 3 h, and 6 h, respectively. Blue and green represent DAPI and C6 fluorescence, which stand for the position of cell nucleus and NPs. The endocytosis of Squ/C6@APS (C) and Squ/C6@APS-IR820 (D) by 4T1 cells was visualized by flow cytometry. Blank represents cells treated with the same volume of medium, which was used as a control (Red). The mean fluorescence intensity (MFI) value (E) of 4T1 cells co-cultured with Squ/C6@APS and Squ/C6@APS-IR820NPs for 1 h, 3 h, and 6 h. Fluorescence image (F) and the mean fluorescence intensity (MFI) value (G) of 4T1 cells co-cultured with Squ/C6@APS-IR820 NPs for 3 h pretreated with 100 μM of probenecid or 50 μM of doxorubicin for 30 min. Invasion of 4T1 cells treated with saline (H), Squ@APS-IR820 NPs (I), MnO 2 @APS-IR820 (J), and Squ@APS-IR820 NPs + MnO 2 @APS-IR820 (K). Invasive cells in every field (L). Data are presented as means ± standard deviation (SD). Differences among groups were evaluated by one-way ANOVA analysis. ∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05. ns, no significant difference. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    Cellular uptake of Squ@APS NPs and Squ@APS-IR820 NPs and <t>transwell</t> invasion assays. Fluorescence image of 4T1 cells co-cultured with Squ/C6@APS (A) and Squ/C6@APS-IR820 (B) at 1 h, 3 h, and 6 h, respectively. Blue and green represent DAPI and C6 fluorescence, which stand for the position of cell nucleus and NPs. The endocytosis of Squ/C6@APS (C) and Squ/C6@APS-IR820 (D) by 4T1 cells was visualized by flow cytometry. Blank represents cells treated with the same volume of medium, which was used as a control (Red). The mean fluorescence intensity (MFI) value (E) of 4T1 cells co-cultured with Squ/C6@APS and Squ/C6@APS-IR820NPs for 1 h, 3 h, and 6 h. Fluorescence image (F) and the mean fluorescence intensity (MFI) value (G) of 4T1 cells co-cultured with Squ/C6@APS-IR820 NPs for 3 h pretreated with 100 μM of probenecid or 50 μM of doxorubicin for 30 min. Invasion of 4T1 cells treated with saline (H), Squ@APS-IR820 NPs (I), MnO 2 @APS-IR820 (J), and Squ@APS-IR820 NPs + MnO 2 @APS-IR820 (K). Invasive cells in every field (L). Data are presented as means ± standard deviation (SD). Differences among groups were evaluated by one-way ANOVA analysis. ∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05. ns, no significant difference. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    Cellular uptake of Squ@APS NPs and Squ@APS-IR820 NPs and <t>transwell</t> invasion assays. Fluorescence image of 4T1 cells co-cultured with Squ/C6@APS (A) and Squ/C6@APS-IR820 (B) at 1 h, 3 h, and 6 h, respectively. Blue and green represent DAPI and C6 fluorescence, which stand for the position of cell nucleus and NPs. The endocytosis of Squ/C6@APS (C) and Squ/C6@APS-IR820 (D) by 4T1 cells was visualized by flow cytometry. Blank represents cells treated with the same volume of medium, which was used as a control (Red). The mean fluorescence intensity (MFI) value (E) of 4T1 cells co-cultured with Squ/C6@APS and Squ/C6@APS-IR820NPs for 1 h, 3 h, and 6 h. Fluorescence image (F) and the mean fluorescence intensity (MFI) value (G) of 4T1 cells co-cultured with Squ/C6@APS-IR820 NPs for 3 h pretreated with 100 μM of probenecid or 50 μM of doxorubicin for 30 min. Invasion of 4T1 cells treated with saline (H), Squ@APS-IR820 NPs (I), MnO 2 @APS-IR820 (J), and Squ@APS-IR820 NPs + MnO 2 @APS-IR820 (K). Invasive cells in every field (L). Data are presented as means ± standard deviation (SD). Differences among groups were evaluated by one-way ANOVA analysis. ∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05. ns, no significant difference. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
    Transwell Chambers In The Presence Of Matrigel Corning 354,480, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Cellular uptake of Squ@APS NPs and Squ@APS-IR820 NPs and transwell invasion assays. Fluorescence image of 4T1 cells co-cultured with Squ/C6@APS (A) and Squ/C6@APS-IR820 (B) at 1 h, 3 h, and 6 h, respectively. Blue and green represent DAPI and C6 fluorescence, which stand for the position of cell nucleus and NPs. The endocytosis of Squ/C6@APS (C) and Squ/C6@APS-IR820 (D) by 4T1 cells was visualized by flow cytometry. Blank represents cells treated with the same volume of medium, which was used as a control (Red). The mean fluorescence intensity (MFI) value (E) of 4T1 cells co-cultured with Squ/C6@APS and Squ/C6@APS-IR820NPs for 1 h, 3 h, and 6 h. Fluorescence image (F) and the mean fluorescence intensity (MFI) value (G) of 4T1 cells co-cultured with Squ/C6@APS-IR820 NPs for 3 h pretreated with 100 μM of probenecid or 50 μM of doxorubicin for 30 min. Invasion of 4T1 cells treated with saline (H), Squ@APS-IR820 NPs (I), MnO 2 @APS-IR820 (J), and Squ@APS-IR820 NPs + MnO 2 @APS-IR820 (K). Invasive cells in every field (L). Data are presented as means ± standard deviation (SD). Differences among groups were evaluated by one-way ANOVA analysis. ∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05. ns, no significant difference. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Materials Today Bio

    Article Title: A MnO 2 -based tumor-seeking nanoplatform for enhanced chemoimmunotherapy against 4T1 breast cancer

    doi: 10.1016/j.mtbio.2025.102000

    Figure Lengend Snippet: Cellular uptake of Squ@APS NPs and Squ@APS-IR820 NPs and transwell invasion assays. Fluorescence image of 4T1 cells co-cultured with Squ/C6@APS (A) and Squ/C6@APS-IR820 (B) at 1 h, 3 h, and 6 h, respectively. Blue and green represent DAPI and C6 fluorescence, which stand for the position of cell nucleus and NPs. The endocytosis of Squ/C6@APS (C) and Squ/C6@APS-IR820 (D) by 4T1 cells was visualized by flow cytometry. Blank represents cells treated with the same volume of medium, which was used as a control (Red). The mean fluorescence intensity (MFI) value (E) of 4T1 cells co-cultured with Squ/C6@APS and Squ/C6@APS-IR820NPs for 1 h, 3 h, and 6 h. Fluorescence image (F) and the mean fluorescence intensity (MFI) value (G) of 4T1 cells co-cultured with Squ/C6@APS-IR820 NPs for 3 h pretreated with 100 μM of probenecid or 50 μM of doxorubicin for 30 min. Invasion of 4T1 cells treated with saline (H), Squ@APS-IR820 NPs (I), MnO 2 @APS-IR820 (J), and Squ@APS-IR820 NPs + MnO 2 @APS-IR820 (K). Invasive cells in every field (L). Data are presented as means ± standard deviation (SD). Differences among groups were evaluated by one-way ANOVA analysis. ∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05. ns, no significant difference. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: The invasive capacity of 4T1 cells was assessed using matrigel-coated transwell chambers (6.5 mm diameter, 8 μm pore size; Corning).

    Techniques: Fluorescence, Cell Culture, Flow Cytometry, Control, Saline, Standard Deviation