celltiter 96 aq ueous non radioactive cell proliferation assay mts kit Search Results


celltiter 96 aq ueous kit  (Promega)
90
Promega celltiter 96 aq ueous kit
Celltiter 96 Aq Ueous Kit, 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
https://www.bioz.com/result/celltiter 96 aq ueous kit/product/Promega
Average 90 stars, based on 1 article reviews
celltiter 96 aq ueous kit - by Bioz Stars, 2026-02
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apoone ® homogeneous caspase 3/7 assay kit  (Promega)
90
Promega apoone ® homogeneous caspase 3/7 assay kit
Apoone ® Homogeneous Caspase 3/7 Assay Kit, 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
https://www.bioz.com/result/apoone ® homogeneous caspase 3/7 assay kit/product/Promega
Average 90 stars, based on 1 article reviews
apoone ® homogeneous caspase 3/7 assay kit - by Bioz Stars, 2026-02
90/100 stars
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cell proliferation assay  (Promega)
90
Promega cell proliferation assay
Cell Proliferation Assay, 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
https://www.bioz.com/result/cell proliferation assay/product/Promega
Average 90 stars, based on 1 article reviews
cell proliferation assay - by Bioz Stars, 2026-02
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mts substrate  (Promega)
90
Promega mts substrate
Comparison of <t>cell</t> <t>proliferation</t> in static and dynamic 3D cultures. (A) Images of live/dead staining show increased cell growth throughout the differentiation process. Red arrows show the necrotic cores that occur under static conditions. Scale bar, 2 mm; (B) The image indicates that there was a high degree of movement, migration of initially immobilized cells, and formation of tissue-like structures in 3D dynamic culture by day 20. Representative images of hematoxylin and eosin-stained cells, their extracellular matrix formed tissue-like assemblies and the cells proliferated more in 3D dynamic conditions by day 20. Scale bars for 2 mm and 200 μm; (C) TEM of 3D cultures at day 15 revealed the presence of necrotic cells or apoptotic bodies (red arrows) and a heterogeneous cell population in static condition whereas no necrotic or apoptotic structures were found in the homogenous dynamically cultured cells. Scale bar, 5.0 µm. 3D, three-dimensional; IPSC, induced pluripotent stem cells; TEM, transmission electron microscopy. (D) Cell Titer Glo profile of encapsulated human IPSCs. Proliferation (normalized to day one, error bars show one standard deviation, n = 3 biological replicates. **** = p < 0.0001; (E) Proliferation plot based on the results of <t>MTS</t> assay assay. Cellular proliferation measured at different time point. All data represt the mean of there independent experiments. P-valueobtained by two way analysis of variance higher on **** p ≤ 0.0001, *** p ≤ 0.001, and ** p ≤ 0.01.
Mts Substrate, 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
https://www.bioz.com/result/mts substrate/product/Promega
Average 90 stars, based on 1 article reviews
mts substrate - by Bioz Stars, 2026-02
90/100 stars
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rnaqueous 96 automated kit  (Thermo Fisher)
N/A
The Ambion RNAqueous 96 Automated Kit is used for automated phenol free total RNA isolation from 100 500 000 cells or 0 1 1 mg tissue using a guanidinium based lysis denaturant and glass fiber
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rnaqueous 96 total rna isolation kit  (Thermo Fisher)
N/A
The RNAqueous 96 Kit is used for high throughput phenol free total RNA isolation from 100 2 000 000 cells or 0 1 1 5 mg of tissue using a guanidinium based lysis denaturant and
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Image Search Results


Comparison of cell proliferation in static and dynamic 3D cultures. (A) Images of live/dead staining show increased cell growth throughout the differentiation process. Red arrows show the necrotic cores that occur under static conditions. Scale bar, 2 mm; (B) The image indicates that there was a high degree of movement, migration of initially immobilized cells, and formation of tissue-like structures in 3D dynamic culture by day 20. Representative images of hematoxylin and eosin-stained cells, their extracellular matrix formed tissue-like assemblies and the cells proliferated more in 3D dynamic conditions by day 20. Scale bars for 2 mm and 200 μm; (C) TEM of 3D cultures at day 15 revealed the presence of necrotic cells or apoptotic bodies (red arrows) and a heterogeneous cell population in static condition whereas no necrotic or apoptotic structures were found in the homogenous dynamically cultured cells. Scale bar, 5.0 µm. 3D, three-dimensional; IPSC, induced pluripotent stem cells; TEM, transmission electron microscopy. (D) Cell Titer Glo profile of encapsulated human IPSCs. Proliferation (normalized to day one, error bars show one standard deviation, n = 3 biological replicates. **** = p < 0.0001; (E) Proliferation plot based on the results of MTS assay assay. Cellular proliferation measured at different time point. All data represt the mean of there independent experiments. P-valueobtained by two way analysis of variance higher on **** p ≤ 0.0001, *** p ≤ 0.001, and ** p ≤ 0.01.

Journal: Frontiers in Bioengineering and Biotechnology

Article Title: Differentiation of human induced pluripotent stem cells into functional lung alveolar epithelial cells in 3D dynamic culture

doi: 10.3389/fbioe.2023.1173149

Figure Lengend Snippet: Comparison of cell proliferation in static and dynamic 3D cultures. (A) Images of live/dead staining show increased cell growth throughout the differentiation process. Red arrows show the necrotic cores that occur under static conditions. Scale bar, 2 mm; (B) The image indicates that there was a high degree of movement, migration of initially immobilized cells, and formation of tissue-like structures in 3D dynamic culture by day 20. Representative images of hematoxylin and eosin-stained cells, their extracellular matrix formed tissue-like assemblies and the cells proliferated more in 3D dynamic conditions by day 20. Scale bars for 2 mm and 200 μm; (C) TEM of 3D cultures at day 15 revealed the presence of necrotic cells or apoptotic bodies (red arrows) and a heterogeneous cell population in static condition whereas no necrotic or apoptotic structures were found in the homogenous dynamically cultured cells. Scale bar, 5.0 µm. 3D, three-dimensional; IPSC, induced pluripotent stem cells; TEM, transmission electron microscopy. (D) Cell Titer Glo profile of encapsulated human IPSCs. Proliferation (normalized to day one, error bars show one standard deviation, n = 3 biological replicates. **** = p < 0.0001; (E) Proliferation plot based on the results of MTS assay assay. Cellular proliferation measured at different time point. All data represt the mean of there independent experiments. P-valueobtained by two way analysis of variance higher on **** p ≤ 0.0001, *** p ≤ 0.001, and ** p ≤ 0.01.

Article Snippet: The MTS substrate (CellTiter 96 ® AQ ueous One Solution Cell Proliferation Assay (MTS) kit, Promega) was prepared in a cell culture medium, added to cells in culture at a final concentration of 0.2–0.5 mg/mL of culture medium, and incubated for 1–4 h. MTS standard curve was calculated using known cell number.

Techniques: Comparison, Staining, Migration, Cell Culture, Transmission Assay, Electron Microscopy, Standard Deviation, MTS Assay