transwell invasion chambers Search Results


90
SPL Life Sciences transwell invasion chambers
Artemisinin significantly inhibited the <t>transwell</t> migration and invasion ability of UM cells in a dose-dependent manner. UM cells were seeded in transwell inserts with or without coating of matrigel and treated with artemisinin for 48 hours. (a, b) Transwell migration and number of migrated UM cells; (c, d) transwell invasion and number of invasive UM cells. The results represent the mean ± SD of three independent experiments versus the control group. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001 were considered statistically significant.
Transwell Invasion Chambers, supplied by SPL 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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Biocoat transwell plates bd biocoat growth factor reduced matrigel invasion chamber
Artemisinin significantly inhibited the <t>transwell</t> migration and invasion ability of UM cells in a dose-dependent manner. UM cells were seeded in transwell inserts with or without coating of matrigel and treated with artemisinin for 48 hours. (a, b) Transwell migration and number of migrated UM cells; (c, d) transwell invasion and number of invasive UM cells. The results represent the mean ± SD of three independent experiments versus the control group. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001 were considered statistically significant.
Transwell Plates Bd Biocoat Growth Factor Reduced Matrigel Invasion Chamber, supplied by Biocoat, 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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Becton Dickinson transwell invasion assay
Artemisinin significantly inhibited the <t>transwell</t> migration and invasion ability of UM cells in a dose-dependent manner. UM cells were seeded in transwell inserts with or without coating of matrigel and treated with artemisinin for 48 hours. (a, b) Transwell migration and number of migrated UM cells; (c, d) transwell invasion and number of invasive UM cells. The results represent the mean ± SD of three independent experiments versus the control group. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001 were considered statistically significant.
Transwell Invasion Assay, supplied by Becton Dickinson, 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/transwell invasion assay/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
transwell invasion assay - by Bioz Stars, 2026-03
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Corning Life Sciences transwell invasion 24-well plates with matrigel invasion chambers
Artemisinin significantly inhibited the <t>transwell</t> migration and invasion ability of UM cells in a dose-dependent manner. UM cells were seeded in transwell inserts with or without coating of matrigel and treated with artemisinin for 48 hours. (a, b) Transwell migration and number of migrated UM cells; (c, d) transwell invasion and number of invasive UM cells. The results represent the mean ± SD of three independent experiments versus the control group. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001 were considered statistically significant.
Transwell Invasion 24 Well Plates With Matrigel Invasion 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/transwell invasion 24-well plates with matrigel invasion chambers/product/Corning Life Sciences
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transwell invasion 24-well plates with matrigel invasion chambers - by Bioz Stars, 2026-03
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Becton Dickinson 24-transwells matrigel invasion chambers
Artemisinin significantly inhibited the <t>transwell</t> migration and invasion ability of UM cells in a dose-dependent manner. UM cells were seeded in transwell inserts with or without coating of matrigel and treated with artemisinin for 48 hours. (a, b) Transwell migration and number of migrated UM cells; (c, d) transwell invasion and number of invasive UM cells. The results represent the mean ± SD of three independent experiments versus the control group. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001 were considered statistically significant.
24 Transwells Matrigel Invasion Chambers, supplied by Becton Dickinson, 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/24-transwells matrigel invasion chambers/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
24-transwells matrigel invasion chambers - by Bioz Stars, 2026-03
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Merck KGaA costar transwell invasion chamber
The TRIM47 gene promoted cell growth in PC cells. TRIM47 mRNA expression (A), cell growth (B), EdU staining assay (C), migration rate (D), <t>Transwell</t> migration assays in an in vitro model of PC via the up-regulation of TRIM47. TRIM47 mRNA expression (E), cell growth (F), EdU assay (G), EdU staining, migration rate (H), Transwell migration assays in an in vitro model of PC via the down-regulation of TRIM47. Vector, negative control group; TRIM47, over-expression of TRIM47 group; Si-nc, si-negative control group; Si-TRIM47, down-regulation of TRIM47 group; **, P<0.01 compared with the Vector group or Si-nc group. TRIM47, tripartite motif 47; PC, prostate cancer; mRNA, messenger RNA; EdU, ethynyl deoxyuridine.
Costar Transwell Invasion Chamber, supplied by Merck KGaA, 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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Corning Life Sciences invasion assay 24 well plate transwell chambers 8um pore size
The TRIM47 gene promoted cell growth in PC cells. TRIM47 mRNA expression (A), cell growth (B), EdU staining assay (C), migration rate (D), <t>Transwell</t> migration assays in an in vitro model of PC via the up-regulation of TRIM47. TRIM47 mRNA expression (E), cell growth (F), EdU assay (G), EdU staining, migration rate (H), Transwell migration assays in an in vitro model of PC via the down-regulation of TRIM47. Vector, negative control group; TRIM47, over-expression of TRIM47 group; Si-nc, si-negative control group; Si-TRIM47, down-regulation of TRIM47 group; **, P<0.01 compared with the Vector group or Si-nc group. TRIM47, tripartite motif 47; PC, prostate cancer; mRNA, messenger RNA; EdU, ethynyl deoxyuridine.
Invasion Assay 24 Well Plate Transwell Chambers 8um Pore Size, 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/invasion assay 24 well plate transwell chambers 8um pore size/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
invasion assay 24 well plate transwell chambers 8um pore size - by Bioz Stars, 2026-03
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Corning Life Sciences cell invasion kit (transwell boyden’s chamber with transwelltm permeable support inserts coated with cultrex bme)
The TRIM47 gene promoted cell growth in PC cells. TRIM47 mRNA expression (A), cell growth (B), EdU staining assay (C), migration rate (D), <t>Transwell</t> migration assays in an in vitro model of PC via the up-regulation of TRIM47. TRIM47 mRNA expression (E), cell growth (F), EdU assay (G), EdU staining, migration rate (H), Transwell migration assays in an in vitro model of PC via the down-regulation of TRIM47. Vector, negative control group; TRIM47, over-expression of TRIM47 group; Si-nc, si-negative control group; Si-TRIM47, down-regulation of TRIM47 group; **, P<0.01 compared with the Vector group or Si-nc group. TRIM47, tripartite motif 47; PC, prostate cancer; mRNA, messenger RNA; EdU, ethynyl deoxyuridine.
Cell Invasion Kit (Transwell Boyden’s Chamber With Transwelltm Permeable Support Inserts Coated With Cultrex Bme), 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/cell invasion kit (transwell boyden’s chamber with transwelltm permeable support inserts coated with cultrex bme)/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
cell invasion kit (transwell boyden’s chamber with transwelltm permeable support inserts coated with cultrex bme) - by Bioz Stars, 2026-03
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Promega transwell invasion chambers
Regulation of invasion by α1-PDX in MG-63 and Saos-2 osteosarcoma cells. The <t>Transwell</t> system was used for detection of the invasion ability of osteosarcoma cells upon α1-PDX treatment. (A) MG-63 control cells. (B) Saos-2 and (C) MG-63 osteosarcoma cells were treated with complete RPMI-1640 or 480 nM α1-PDX, seeded in the upper chamber at a density of 4×10 4 cells per chamber and allowed to migrate through the chamber pore for 12 h. Subsequently, the number of cells per field that had migrated to the bottom surface of the filter was counted. (D) The mean and standard error from three separate experiments are shown. Statistical analyses were performed using the t-test and one-way analysis of variance. * P<0.05 indicates a significant difference compared with the control group. α1-PDX, α1-antitrypsin Portland.
Transwell Invasion Chambers, supplied by Promega, 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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transwell invasion chambers - by Bioz Stars, 2026-03
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Corning Life Sciences 24-well plate transwell-invasion chamber with poresize filter inserts
Regulation of invasion by α1-PDX in MG-63 and Saos-2 osteosarcoma cells. The <t>Transwell</t> system was used for detection of the invasion ability of osteosarcoma cells upon α1-PDX treatment. (A) MG-63 control cells. (B) Saos-2 and (C) MG-63 osteosarcoma cells were treated with complete RPMI-1640 or 480 nM α1-PDX, seeded in the upper chamber at a density of 4×10 4 cells per chamber and allowed to migrate through the chamber pore for 12 h. Subsequently, the number of cells per field that had migrated to the bottom surface of the filter was counted. (D) The mean and standard error from three separate experiments are shown. Statistical analyses were performed using the t-test and one-way analysis of variance. * P<0.05 indicates a significant difference compared with the control group. α1-PDX, α1-antitrypsin Portland.
24 Well Plate Transwell Invasion Chamber With Poresize Filter Inserts, 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/24-well plate transwell-invasion chamber with poresize filter inserts/product/Corning Life Sciences
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Becton Dickinson transwell 8.0- m invasion chambers
Regulation of invasion by α1-PDX in MG-63 and Saos-2 osteosarcoma cells. The <t>Transwell</t> system was used for detection of the invasion ability of osteosarcoma cells upon α1-PDX treatment. (A) MG-63 control cells. (B) Saos-2 and (C) MG-63 osteosarcoma cells were treated with complete RPMI-1640 or 480 nM α1-PDX, seeded in the upper chamber at a density of 4×10 4 cells per chamber and allowed to migrate through the chamber pore for 12 h. Subsequently, the number of cells per field that had migrated to the bottom surface of the filter was counted. (D) The mean and standard error from three separate experiments are shown. Statistical analyses were performed using the t-test and one-way analysis of variance. * P<0.05 indicates a significant difference compared with the control group. α1-PDX, α1-antitrypsin Portland.
Transwell 8.0 M Invasion Chambers, supplied by Becton Dickinson, 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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Fisher Scientific boyden chamber transwell pre-coated with growth factor-reduced matrigel matrix
Regulation of invasion by α1-PDX in MG-63 and Saos-2 osteosarcoma cells. The <t>Transwell</t> system was used for detection of the invasion ability of osteosarcoma cells upon α1-PDX treatment. (A) MG-63 control cells. (B) Saos-2 and (C) MG-63 osteosarcoma cells were treated with complete RPMI-1640 or 480 nM α1-PDX, seeded in the upper chamber at a density of 4×10 4 cells per chamber and allowed to migrate through the chamber pore for 12 h. Subsequently, the number of cells per field that had migrated to the bottom surface of the filter was counted. (D) The mean and standard error from three separate experiments are shown. Statistical analyses were performed using the t-test and one-way analysis of variance. * P<0.05 indicates a significant difference compared with the control group. α1-PDX, α1-antitrypsin Portland.
Boyden Chamber Transwell Pre Coated With Growth Factor Reduced Matrigel Matrix, supplied by Fisher Scientific, 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


Artemisinin significantly inhibited the transwell migration and invasion ability of UM cells in a dose-dependent manner. UM cells were seeded in transwell inserts with or without coating of matrigel and treated with artemisinin for 48 hours. (a, b) Transwell migration and number of migrated UM cells; (c, d) transwell invasion and number of invasive UM cells. The results represent the mean ± SD of three independent experiments versus the control group. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001 were considered statistically significant.

Journal: Oxidative Medicine and Cellular Longevity

Article Title: Artemisinin Inhibits the Migration and Invasion in Uveal Melanoma via Inhibition of the PI3K/AKT/mTOR Signaling Pathway

doi: 10.1155/2021/9911537

Figure Lengend Snippet: Artemisinin significantly inhibited the transwell migration and invasion ability of UM cells in a dose-dependent manner. UM cells were seeded in transwell inserts with or without coating of matrigel and treated with artemisinin for 48 hours. (a, b) Transwell migration and number of migrated UM cells; (c, d) transwell invasion and number of invasive UM cells. The results represent the mean ± SD of three independent experiments versus the control group. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001 were considered statistically significant.

Article Snippet: Transwell invasion chambers were purchased from SPL Life Sciences (Korea), and matrix matrigel was obtained from BD Biosciences (San Jose, CA).

Techniques: Migration, Control

The TRIM47 gene promoted cell growth in PC cells. TRIM47 mRNA expression (A), cell growth (B), EdU staining assay (C), migration rate (D), Transwell migration assays in an in vitro model of PC via the up-regulation of TRIM47. TRIM47 mRNA expression (E), cell growth (F), EdU assay (G), EdU staining, migration rate (H), Transwell migration assays in an in vitro model of PC via the down-regulation of TRIM47. Vector, negative control group; TRIM47, over-expression of TRIM47 group; Si-nc, si-negative control group; Si-TRIM47, down-regulation of TRIM47 group; **, P<0.01 compared with the Vector group or Si-nc group. TRIM47, tripartite motif 47; PC, prostate cancer; mRNA, messenger RNA; EdU, ethynyl deoxyuridine.

Journal: Translational Andrology and Urology

Article Title: TRIM47 promotes the Warburg effect and reduces ferroptosis in prostate cancer by FBP1 and FOXO1

doi: 10.21037/tau-23-605

Figure Lengend Snippet: The TRIM47 gene promoted cell growth in PC cells. TRIM47 mRNA expression (A), cell growth (B), EdU staining assay (C), migration rate (D), Transwell migration assays in an in vitro model of PC via the up-regulation of TRIM47. TRIM47 mRNA expression (E), cell growth (F), EdU assay (G), EdU staining, migration rate (H), Transwell migration assays in an in vitro model of PC via the down-regulation of TRIM47. Vector, negative control group; TRIM47, over-expression of TRIM47 group; Si-nc, si-negative control group; Si-TRIM47, down-regulation of TRIM47 group; **, P<0.01 compared with the Vector group or Si-nc group. TRIM47, tripartite motif 47; PC, prostate cancer; mRNA, messenger RNA; EdU, ethynyl deoxyuridine.

Article Snippet: The migration assays were performed using the Costar Transwell Invasion chamber (Merck KgaA, Shanghai, China) in accordance with the manufacturer’s instructions ( , ).

Techniques: Expressing, Staining, Migration, In Vitro, EdU Assay, Plasmid Preparation, Negative Control, Over Expression

Regulation of invasion by α1-PDX in MG-63 and Saos-2 osteosarcoma cells. The Transwell system was used for detection of the invasion ability of osteosarcoma cells upon α1-PDX treatment. (A) MG-63 control cells. (B) Saos-2 and (C) MG-63 osteosarcoma cells were treated with complete RPMI-1640 or 480 nM α1-PDX, seeded in the upper chamber at a density of 4×10 4 cells per chamber and allowed to migrate through the chamber pore for 12 h. Subsequently, the number of cells per field that had migrated to the bottom surface of the filter was counted. (D) The mean and standard error from three separate experiments are shown. Statistical analyses were performed using the t-test and one-way analysis of variance. * P<0.05 indicates a significant difference compared with the control group. α1-PDX, α1-antitrypsin Portland.

Journal: Oncology Letters

Article Title: A furin inhibitor downregulates osteosarcoma cell migration by downregulating the expression levels of MT1-MMP via the Wnt signaling pathway

doi: 10.3892/ol.2014.1839

Figure Lengend Snippet: Regulation of invasion by α1-PDX in MG-63 and Saos-2 osteosarcoma cells. The Transwell system was used for detection of the invasion ability of osteosarcoma cells upon α1-PDX treatment. (A) MG-63 control cells. (B) Saos-2 and (C) MG-63 osteosarcoma cells were treated with complete RPMI-1640 or 480 nM α1-PDX, seeded in the upper chamber at a density of 4×10 4 cells per chamber and allowed to migrate through the chamber pore for 12 h. Subsequently, the number of cells per field that had migrated to the bottom surface of the filter was counted. (D) The mean and standard error from three separate experiments are shown. Statistical analyses were performed using the t-test and one-way analysis of variance. * P<0.05 indicates a significant difference compared with the control group. α1-PDX, α1-antitrypsin Portland.

Article Snippet: Other reagents were used, including anti-mouse-IgG-HRP and anti-rabbit-IgG-HRP (BD Biosciences, CA, USA) and Transwell invasion chambers (Promega, Madison, WI, USA).

Techniques: Control