vivo optical imaging analyses Search Results


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JENOPTIK Inc transmission light microscope with progres capture system
Inhibition of S100A8, S100A9, and LGALS3BP expression impairs migration of pancreatic cancer cell line L3.6sl. ( A ) Representative images of the specific knockdown cells (shS100A8, shS100A9, and shLGALS3BP) compared to non-target control shRNA cells (sh ctrl) shown are after 0.0, 6.0, 12.0, and 24.0 h. Black lines enclose areas free of migratory cancer cells. Quantification of migration ability over time ( B ): 0.0 h control shRNA area was set to 0%; all other values were normalized accordingly. Measurements were done with the <t>ProgRes</t> Software. Error bars represent standard deviations of six measurements. Statistical significances were assessed by a two-way ANOVA followed by a Dunnett’s post-hoc test (* for p ≤ 0.05, ** for p ≤ 0.01. and *** for p ≤ 0.001, n = 6).
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Guangzhou Biolight Biotechnology Co Ltd vivo optical imaging system
Inhibition of S100A8, S100A9, and LGALS3BP expression impairs migration of pancreatic cancer cell line L3.6sl. ( A ) Representative images of the specific knockdown cells (shS100A8, shS100A9, and shLGALS3BP) compared to non-target control shRNA cells (sh ctrl) shown are after 0.0, 6.0, 12.0, and 24.0 h. Black lines enclose areas free of migratory cancer cells. Quantification of migration ability over time ( B ): 0.0 h control shRNA area was set to 0%; all other values were normalized accordingly. Measurements were done with the <t>ProgRes</t> Software. Error bars represent standard deviations of six measurements. Statistical significances were assessed by a two-way ANOVA followed by a Dunnett’s post-hoc test (* for p ≤ 0.05, ** for p ≤ 0.01. and *** for p ≤ 0.001, n = 6).
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ISUZU Optics hsi analyser spectral image software
Inhibition of S100A8, S100A9, and LGALS3BP expression impairs migration of pancreatic cancer cell line L3.6sl. ( A ) Representative images of the specific knockdown cells (shS100A8, shS100A9, and shLGALS3BP) compared to non-target control shRNA cells (sh ctrl) shown are after 0.0, 6.0, 12.0, and 24.0 h. Black lines enclose areas free of migratory cancer cells. Quantification of migration ability over time ( B ): 0.0 h control shRNA area was set to 0%; all other values were normalized accordingly. Measurements were done with the <t>ProgRes</t> Software. Error bars represent standard deviations of six measurements. Statistical significances were assessed by a two-way ANOVA followed by a Dunnett’s post-hoc test (* for p ≤ 0.05, ** for p ≤ 0.01. and *** for p ≤ 0.001, n = 6).
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ISUZU Optics spectral image analyser
Inhibition of S100A8, S100A9, and LGALS3BP expression impairs migration of pancreatic cancer cell line L3.6sl. ( A ) Representative images of the specific knockdown cells (shS100A8, shS100A9, and shLGALS3BP) compared to non-target control shRNA cells (sh ctrl) shown are after 0.0, 6.0, 12.0, and 24.0 h. Black lines enclose areas free of migratory cancer cells. Quantification of migration ability over time ( B ): 0.0 h control shRNA area was set to 0%; all other values were normalized accordingly. Measurements were done with the <t>ProgRes</t> Software. Error bars represent standard deviations of six measurements. Statistical significances were assessed by a two-way ANOVA followed by a Dunnett’s post-hoc test (* for p ≤ 0.05, ** for p ≤ 0.01. and *** for p ≤ 0.001, n = 6).
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96
Revvity ivis optical imaging platform
Inhibition of S100A8, S100A9, and LGALS3BP expression impairs migration of pancreatic cancer cell line L3.6sl. ( A ) Representative images of the specific knockdown cells (shS100A8, shS100A9, and shLGALS3BP) compared to non-target control shRNA cells (sh ctrl) shown are after 0.0, 6.0, 12.0, and 24.0 h. Black lines enclose areas free of migratory cancer cells. Quantification of migration ability over time ( B ): 0.0 h control shRNA area was set to 0%; all other values were normalized accordingly. Measurements were done with the <t>ProgRes</t> Software. Error bars represent standard deviations of six measurements. Statistical significances were assessed by a two-way ANOVA followed by a Dunnett’s post-hoc test (* for p ≤ 0.05, ** for p ≤ 0.01. and *** for p ≤ 0.001, n = 6).
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CRI Medical Devices whole-body optical imaging system cri's new maestrotm ex in-vivo imaging system
Inhibition of S100A8, S100A9, and LGALS3BP expression impairs migration of pancreatic cancer cell line L3.6sl. ( A ) Representative images of the specific knockdown cells (shS100A8, shS100A9, and shLGALS3BP) compared to non-target control shRNA cells (sh ctrl) shown are after 0.0, 6.0, 12.0, and 24.0 h. Black lines enclose areas free of migratory cancer cells. Quantification of migration ability over time ( B ): 0.0 h control shRNA area was set to 0%; all other values were normalized accordingly. Measurements were done with the <t>ProgRes</t> Software. Error bars represent standard deviations of six measurements. Statistical significances were assessed by a two-way ANOVA followed by a Dunnett’s post-hoc test (* for p ≤ 0.05, ** for p ≤ 0.01. and *** for p ≤ 0.001, n = 6).
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Carestream Molecular Imaging in-vivo xtreme optical and x-ray small-animal imaging system
Inhibition of S100A8, S100A9, and LGALS3BP expression impairs migration of pancreatic cancer cell line L3.6sl. ( A ) Representative images of the specific knockdown cells (shS100A8, shS100A9, and shLGALS3BP) compared to non-target control shRNA cells (sh ctrl) shown are after 0.0, 6.0, 12.0, and 24.0 h. Black lines enclose areas free of migratory cancer cells. Quantification of migration ability over time ( B ): 0.0 h control shRNA area was set to 0%; all other values were normalized accordingly. Measurements were done with the <t>ProgRes</t> Software. Error bars represent standard deviations of six measurements. Statistical significances were assessed by a two-way ANOVA followed by a Dunnett’s post-hoc test (* for p ≤ 0.05, ** for p ≤ 0.01. and *** for p ≤ 0.001, n = 6).
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Image Search Results


Inhibition of S100A8, S100A9, and LGALS3BP expression impairs migration of pancreatic cancer cell line L3.6sl. ( A ) Representative images of the specific knockdown cells (shS100A8, shS100A9, and shLGALS3BP) compared to non-target control shRNA cells (sh ctrl) shown are after 0.0, 6.0, 12.0, and 24.0 h. Black lines enclose areas free of migratory cancer cells. Quantification of migration ability over time ( B ): 0.0 h control shRNA area was set to 0%; all other values were normalized accordingly. Measurements were done with the ProgRes Software. Error bars represent standard deviations of six measurements. Statistical significances were assessed by a two-way ANOVA followed by a Dunnett’s post-hoc test (* for p ≤ 0.05, ** for p ≤ 0.01. and *** for p ≤ 0.001, n = 6).

Journal: Cells

Article Title: Proteins and Molecular Pathways Relevant for the Malignant Properties of Tumor-Initiating Pancreatic Cancer Cells

doi: 10.3390/cells9061397

Figure Lengend Snippet: Inhibition of S100A8, S100A9, and LGALS3BP expression impairs migration of pancreatic cancer cell line L3.6sl. ( A ) Representative images of the specific knockdown cells (shS100A8, shS100A9, and shLGALS3BP) compared to non-target control shRNA cells (sh ctrl) shown are after 0.0, 6.0, 12.0, and 24.0 h. Black lines enclose areas free of migratory cancer cells. Quantification of migration ability over time ( B ): 0.0 h control shRNA area was set to 0%; all other values were normalized accordingly. Measurements were done with the ProgRes Software. Error bars represent standard deviations of six measurements. Statistical significances were assessed by a two-way ANOVA followed by a Dunnett’s post-hoc test (* for p ≤ 0.05, ** for p ≤ 0.01. and *** for p ≤ 0.001, n = 6).

Article Snippet: Cell movement was assessed after 0.0, 6.0, 12.0, and 24.0 h and documented using a transmission light microscope with ProgRes capture system (Jenoptik GmbH, Jena, Germany).

Techniques: Inhibition, Expressing, Migration, Knockdown, Control, shRNA, Software