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Corning Life Sciences matrigel invasion chambers
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/matrigel invasion chambers/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
matrigel invasion chambers - by Bioz Stars, 2026-03
90/100 stars

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Corning Life Sciences transwell chamber matrigel® invasion chamber 8.0micron
TIMM8A knockdown inhibited the migration and invasion of breast cancer in vitro. ( A – C ) Migration capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by scratch experiment. Area Recovery (%) = (initial scratch area—final scratch area)/initial scratch area × 100%. ( D – F ) Migration capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by <t>transwell</t> migration assay. ( G – I ) Invasion capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by transwell invasion assay. ( J – R ) The expression levels of NF-κB p65 and EMT-related proteins, including α-SMA, Vimentin, E-cadherin and N-cadherin in MCF7 and MDA-MB-231 cells after knockdown of TIMM8A. GAPDH was used as a loading control. The results shown are representative of at least three independent experiments. EMT, epithelial-mesenchymal transition. The student’s t-test or one-way ANOVA was used to detect the differences among groups. * P < 0.05, ** P < 0.01, *** P < 0.001. Samples were derived from the same experiment and gels/blots were processed in parallel. Original blots/gels are presented in the Supplementary File.
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Corning Life Sciences matrigel invasion chamber 354480
TIMM8A knockdown inhibited the migration and invasion of breast cancer in vitro. ( A – C ) Migration capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by scratch experiment. Area Recovery (%) = (initial scratch area—final scratch area)/initial scratch area × 100%. ( D – F ) Migration capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by <t>transwell</t> migration assay. ( G – I ) Invasion capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by transwell invasion assay. ( J – R ) The expression levels of NF-κB p65 and EMT-related proteins, including α-SMA, Vimentin, E-cadherin and N-cadherin in MCF7 and MDA-MB-231 cells after knockdown of TIMM8A. GAPDH was used as a loading control. The results shown are representative of at least three independent experiments. EMT, epithelial-mesenchymal transition. The student’s t-test or one-way ANOVA was used to detect the differences among groups. * P < 0.05, ** P < 0.01, *** P < 0.001. Samples were derived from the same experiment and gels/blots were processed in parallel. Original blots/gels are presented in the Supplementary File.
Matrigel Invasion Chamber 354480, 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 invasion chamber 354480/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
matrigel invasion chamber 354480 - by Bioz Stars, 2026-03
90/100 stars
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TIMM8A knockdown inhibited the migration and invasion of breast cancer in vitro. ( A – C ) Migration capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by scratch experiment. Area Recovery (%) = (initial scratch area—final scratch area)/initial scratch area × 100%. ( D – F ) Migration capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by transwell migration assay. ( G – I ) Invasion capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by transwell invasion assay. ( J – R ) The expression levels of NF-κB p65 and EMT-related proteins, including α-SMA, Vimentin, E-cadherin and N-cadherin in MCF7 and MDA-MB-231 cells after knockdown of TIMM8A. GAPDH was used as a loading control. The results shown are representative of at least three independent experiments. EMT, epithelial-mesenchymal transition. The student’s t-test or one-way ANOVA was used to detect the differences among groups. * P < 0.05, ** P < 0.01, *** P < 0.001. Samples were derived from the same experiment and gels/blots were processed in parallel. Original blots/gels are presented in the Supplementary File.

Journal: Scientific Reports

Article Title: The oncogenic role of TIMM8A in cancer and the mechanistic insights into the function in breast cancer cells

doi: 10.1038/s41598-025-03331-x

Figure Lengend Snippet: TIMM8A knockdown inhibited the migration and invasion of breast cancer in vitro. ( A – C ) Migration capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by scratch experiment. Area Recovery (%) = (initial scratch area—final scratch area)/initial scratch area × 100%. ( D – F ) Migration capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by transwell migration assay. ( G – I ) Invasion capacity of MCF7 and MDA-MB-231 cells after knockdown of TIMM8A assayed by transwell invasion assay. ( J – R ) The expression levels of NF-κB p65 and EMT-related proteins, including α-SMA, Vimentin, E-cadherin and N-cadherin in MCF7 and MDA-MB-231 cells after knockdown of TIMM8A. GAPDH was used as a loading control. The results shown are representative of at least three independent experiments. EMT, epithelial-mesenchymal transition. The student’s t-test or one-way ANOVA was used to detect the differences among groups. * P < 0.05, ** P < 0.01, *** P < 0.001. Samples were derived from the same experiment and gels/blots were processed in parallel. Original blots/gels are presented in the Supplementary File.

Article Snippet: The fundamental procedures were as follows: the transwell chamber (invasion assay: Matrigel® invasion chamber 8.0micron, Corning, USA; migration assay: 24 well multiwell insert System 8.0micron, Falcon, USA) is placed in the 24-well plate, the chamber is called the upper chamber and the plate is called the lower chamber.

Techniques: Knockdown, Migration, In Vitro, Transwell Migration Assay, Transwell Invasion Assay, Expressing, Control, Derivative Assay