v. 2018b software Search Results


incucyte 2018b software  (Sartorius AG)
99
Sartorius AG incucyte 2018b software
Mutant SF3B1 promoted EMT phenotypes in prolactinoma. A GO functional enrichment analysis of DEGs in Sf3b1 mutant vs. wild-type GH3 cells. B Scanning electron microscopy (SEM; upper) and confocal images of the actin cytoskeleton stained with rhodamine–phalloidin (lower) of Sf3b1 wild-type and mutant GH3 cells; scale bar: 10 μm. C Scratch wound healing assays were performed using Sf3b1 wild-type and mutant GH3 cells; scale bar: 200 μm. Relative scratch widths are shown over time ( n = 3; mean ± SD shown below; P values by Student’s test). D Kinetics of wound confluence over 96 h were analyzed using IncuCyte <t>2018B</t> software (Essen Bioscience). The results are expressed as mean ± SD, n = 3. P values by two-way ANOVA; **** P < 0.0001. E DLG1, E-cadherin, N-cadherin, Vimentin, and Snail levels in Sf3b1 wild-type and mutant GH3 cells transduced with or without Dlg1-FLAG cDNA. G Immunofluorescence staining of E-cadherin and Vimentin in rat prolactinoma tumors stereotactically injected with Ad-null, Ad-SF3B1 WT , and Ad-SF3B1 R625H ; scale bar: 50 μm. F Representative immunohistochemical staining for E-cadherin, N-cadherin, and Snail in SF3B1 mutant and wild-type human prolactinoma tumors; scale bar: 50 μm. H Venn diagram of the numbers of differentially spliced (q < 0.05; t test) and differentially expressed genes (q < 0.05; DESeq2) in SF3B1 mutant human prolactinoma and GH3 samples
Incucyte 2018b Software, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/v%2E+2018b+software/pmc08762886-168-11-14?v=Sartorius+AG
Average 99 stars, based on 1 article reviews
incucyte 2018b software - by Bioz Stars, 2026-07
99/100 stars
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origin pro software  (OriginLab corp)
90
OriginLab corp origin pro software
Mutant SF3B1 promoted EMT phenotypes in prolactinoma. A GO functional enrichment analysis of DEGs in Sf3b1 mutant vs. wild-type GH3 cells. B Scanning electron microscopy (SEM; upper) and confocal images of the actin cytoskeleton stained with rhodamine–phalloidin (lower) of Sf3b1 wild-type and mutant GH3 cells; scale bar: 10 μm. C Scratch wound healing assays were performed using Sf3b1 wild-type and mutant GH3 cells; scale bar: 200 μm. Relative scratch widths are shown over time ( n = 3; mean ± SD shown below; P values by Student’s test). D Kinetics of wound confluence over 96 h were analyzed using IncuCyte <t>2018B</t> software (Essen Bioscience). The results are expressed as mean ± SD, n = 3. P values by two-way ANOVA; **** P < 0.0001. E DLG1, E-cadherin, N-cadherin, Vimentin, and Snail levels in Sf3b1 wild-type and mutant GH3 cells transduced with or without Dlg1-FLAG cDNA. G Immunofluorescence staining of E-cadherin and Vimentin in rat prolactinoma tumors stereotactically injected with Ad-null, Ad-SF3B1 WT , and Ad-SF3B1 R625H ; scale bar: 50 μm. F Representative immunohistochemical staining for E-cadherin, N-cadherin, and Snail in SF3B1 mutant and wild-type human prolactinoma tumors; scale bar: 50 μm. H Venn diagram of the numbers of differentially spliced (q < 0.05; t test) and differentially expressed genes (q < 0.05; DESeq2) in SF3B1 mutant human prolactinoma and GH3 samples
Origin Pro Software, supplied by OriginLab corp, 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/product/v%2E+2018b+software/pmc07145343-234-6-11?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
origin pro software - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

Image Search Results


Mutant SF3B1 promoted EMT phenotypes in prolactinoma. A GO functional enrichment analysis of DEGs in Sf3b1 mutant vs. wild-type GH3 cells. B Scanning electron microscopy (SEM; upper) and confocal images of the actin cytoskeleton stained with rhodamine–phalloidin (lower) of Sf3b1 wild-type and mutant GH3 cells; scale bar: 10 μm. C Scratch wound healing assays were performed using Sf3b1 wild-type and mutant GH3 cells; scale bar: 200 μm. Relative scratch widths are shown over time ( n = 3; mean ± SD shown below; P values by Student’s test). D Kinetics of wound confluence over 96 h were analyzed using IncuCyte 2018B software (Essen Bioscience). The results are expressed as mean ± SD, n = 3. P values by two-way ANOVA; **** P < 0.0001. E DLG1, E-cadherin, N-cadherin, Vimentin, and Snail levels in Sf3b1 wild-type and mutant GH3 cells transduced with or without Dlg1-FLAG cDNA. G Immunofluorescence staining of E-cadherin and Vimentin in rat prolactinoma tumors stereotactically injected with Ad-null, Ad-SF3B1 WT , and Ad-SF3B1 R625H ; scale bar: 50 μm. F Representative immunohistochemical staining for E-cadherin, N-cadherin, and Snail in SF3B1 mutant and wild-type human prolactinoma tumors; scale bar: 50 μm. H Venn diagram of the numbers of differentially spliced (q < 0.05; t test) and differentially expressed genes (q < 0.05; DESeq2) in SF3B1 mutant human prolactinoma and GH3 samples

Journal: Journal of Experimental & Clinical Cancer Research : CR

Article Title: The SF3B1 R625H mutation promotes prolactinoma tumor progression through aberrant splicing of DLG1

doi: 10.1186/s13046-022-02245-0

Figure Lengend Snippet: Mutant SF3B1 promoted EMT phenotypes in prolactinoma. A GO functional enrichment analysis of DEGs in Sf3b1 mutant vs. wild-type GH3 cells. B Scanning electron microscopy (SEM; upper) and confocal images of the actin cytoskeleton stained with rhodamine–phalloidin (lower) of Sf3b1 wild-type and mutant GH3 cells; scale bar: 10 μm. C Scratch wound healing assays were performed using Sf3b1 wild-type and mutant GH3 cells; scale bar: 200 μm. Relative scratch widths are shown over time ( n = 3; mean ± SD shown below; P values by Student’s test). D Kinetics of wound confluence over 96 h were analyzed using IncuCyte 2018B software (Essen Bioscience). The results are expressed as mean ± SD, n = 3. P values by two-way ANOVA; **** P < 0.0001. E DLG1, E-cadherin, N-cadherin, Vimentin, and Snail levels in Sf3b1 wild-type and mutant GH3 cells transduced with or without Dlg1-FLAG cDNA. G Immunofluorescence staining of E-cadherin and Vimentin in rat prolactinoma tumors stereotactically injected with Ad-null, Ad-SF3B1 WT , and Ad-SF3B1 R625H ; scale bar: 50 μm. F Representative immunohistochemical staining for E-cadherin, N-cadherin, and Snail in SF3B1 mutant and wild-type human prolactinoma tumors; scale bar: 50 μm. H Venn diagram of the numbers of differentially spliced (q < 0.05; t test) and differentially expressed genes (q < 0.05; DESeq2) in SF3B1 mutant human prolactinoma and GH3 samples

Article Snippet: D Kinetics of wound confluence over 96 h were analyzed using IncuCyte 2018B software (Essen Bioscience).

Techniques: Mutagenesis, Functional Assay, Electron Microscopy, Staining, Software, Transduction, Immunofluorescence, Injection, Immunohistochemistry