xcellence/cell^r software (Evident Corporation)
90
Structured Review
Evident Corporation
xcellence/cell^r software
Xcellence/Cell^R Software, supplied by Evident Corporation, 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/cell+r+software/dp2+software/pm39134648-215-21-23
Average 90 stars, based on 1 article reviews
Xcellence/Cell^R Software, supplied by Evident Corporation, 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/cell+r+software/dp2+software/pm39134648-215-21-23
Average 90 stars, based on 1 article reviews
xcellence/cell^r software - by Bioz Stars,
2026-09
90/100 stars
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Microscopy:Article Title: Transferable Matrixes Produced from Decellularized Extracellular Matrix Promote Proliferation and Osteogenic Differentiation of Mesenchymal Stem Cells and Facilitate Scale-Up. Article Snippet: Decellularized extracellular matrixes (dECM) derived from mesenchymal stem cell (MSC) cultures have recently emerged as cell culture substrates that improve the proliferation, differentiation, and maintenance of MSC phenotype during ex vivo expansion.. These biomaterials have considerable potential in the fields of stem cell biology, tissue engineering, and regenerative medicine.. Processing the dECMs into concentrated solutions of biomolecules that enable the useful properties of the native dECM to be transferred to a new surface via a simple adsorption step would greatly increase the usefulness and impact of this technology. Article Title: Neurite Outgrowth of Mature Retinal Ganglion Cells and PC12 Cells Requires Activity of CK1δ and CK1ε Article Snippet: D4476 was applied using transfection reagent (Effectene, Qiagen, Hilden, Germany) as described previously . .. The cells were monitored for 4 h and phase contrast or bright field time-lapse recordings were taken under 40× magnification using the Olympus IX81 microscope (Olympus, Hamburg, Germany) and the Article Title: Stathmin Regulates Keratinocyte Proliferation and Migration during Cutaneous Regeneration Article Snippet: .. Cell migration was documented by time-lapse microscopy at 37°C, 5% CO 2 and 40% humidity using the Cell^R Imaging Station (Olympus, IX-81-ZDC microscope, C10600 ORCA-R 2 camera) every 20 to 60 min for 24 or 48 h. Samples were visualized using the following objectives: 10x UPLanF/, NA = 0.3, 20x UPLanSApo, NA =0.75, 40x UPLanSApo, NA = 0.95 (Olympus) and analysed by the Fluorescence:Article Title: Transferable Matrixes Produced from Decellularized Extracellular Matrix Promote Proliferation and Osteogenic Differentiation of Mesenchymal Stem Cells and Facilitate Scale-Up. Article Snippet: Decellularized extracellular matrixes (dECM) derived from mesenchymal stem cell (MSC) cultures have recently emerged as cell culture substrates that improve the proliferation, differentiation, and maintenance of MSC phenotype during ex vivo expansion.. These biomaterials have considerable potential in the fields of stem cell biology, tissue engineering, and regenerative medicine.. Processing the dECMs into concentrated solutions of biomolecules that enable the useful properties of the native dECM to be transferred to a new surface via a simple adsorption step would greatly increase the usefulness and impact of this technology. Imaging:Article Title: Transferable Matrixes Produced from Decellularized Extracellular Matrix Promote Proliferation and Osteogenic Differentiation of Mesenchymal Stem Cells and Facilitate Scale-Up. Article Snippet: Decellularized extracellular matrixes (dECM) derived from mesenchymal stem cell (MSC) cultures have recently emerged as cell culture substrates that improve the proliferation, differentiation, and maintenance of MSC phenotype during ex vivo expansion.. These biomaterials have considerable potential in the fields of stem cell biology, tissue engineering, and regenerative medicine.. Processing the dECMs into concentrated solutions of biomolecules that enable the useful properties of the native dECM to be transferred to a new surface via a simple adsorption step would greatly increase the usefulness and impact of this technology. Article Title: Stathmin Regulates Keratinocyte Proliferation and Migration during Cutaneous Regeneration Article Snippet: .. Cell migration was documented by time-lapse microscopy at 37°C, 5% CO 2 and 40% humidity using the Cell^R Imaging Station (Olympus, IX-81-ZDC microscope, C10600 ORCA-R 2 camera) every 20 to 60 min for 24 or 48 h. Samples were visualized using the following objectives: 10x UPLanF/, NA = 0.3, 20x UPLanSApo, NA =0.75, 40x UPLanSApo, NA = 0.95 (Olympus) and analysed by the Software:Article Title: Transferable Matrixes Produced from Decellularized Extracellular Matrix Promote Proliferation and Osteogenic Differentiation of Mesenchymal Stem Cells and Facilitate Scale-Up. Article Snippet: Decellularized extracellular matrixes (dECM) derived from mesenchymal stem cell (MSC) cultures have recently emerged as cell culture substrates that improve the proliferation, differentiation, and maintenance of MSC phenotype during ex vivo expansion.. These biomaterials have considerable potential in the fields of stem cell biology, tissue engineering, and regenerative medicine.. Processing the dECMs into concentrated solutions of biomolecules that enable the useful properties of the native dECM to be transferred to a new surface via a simple adsorption step would greatly increase the usefulness and impact of this technology. Article Title: Anti-Inflammatory, Anti-Oxidative and Anti-Apoptotic Effects of Thymol and 24-Epibrassinolide in Zebrafish Larvae Article Snippet: Then, fluorescent images were obtained under an inverted microscope (IX 51, Olympus, Antwerp, Belgium) equipped with an Olympus U-RFL-T fluorescent light source (Olympus, Antwerp, Belgium) and FITC filter, using a 4X Olympus UIS-2 objective lens (Olympus Co., Ltd., Tokyo, Japan). .. The data were acquired using the Article Title: Reconstruction of Mouse Testicular Cellular Microenvironments in Long-Term Seminiferous Tubule Culture Article Snippet: Frames were captured at defined intervals (5 sec to 30 min) using Olympus DBH1 camera attached to a Olympus IX71 microscope with 10X phase-contrast objective. .. All images were acquired digitally using Article Title: Hexokinase II Detachment from Mitochondria Triggers Apoptosis through the Permeability Transition Pore Independent of Voltage-Dependent Anion Channels Article Snippet: .. Data were acquired and analyzed by using Article Title: cAMP/PKA signaling balances respiratory activity with mitochondria dependent apoptosis via transcriptional regulation Article Snippet: .. Images were captured using a Hammamatsu ORCA AG digital camera using Article Title: Cyclosporine A in Ullrich Congenital Muscular Dystrophy: Long-Term Results Article Snippet: Primary cell cultures obtained from patient biopsies were plated within 4 h of the surgical biopsy in complete medium plus 20% FCS on laminin/poly-L-lysine-coated coverslips (BD Laboratories), and allowed to attach and spread for 9–14 h. The medium was then replaced with serum-free DMEM supplemented with 10 nM TMRM for 30 min, and cellular fluorescence images were acquired with an Olympus IX71/IX51 inverted microscope, equipped with a xenon light source (75 W) for epifluorescence illumination and with a 12-bit digital cooled CCD camera (Micromax, Princeton Instruments). .. Data were acquired and analyzed using Article Title: Neurite Outgrowth of Mature Retinal Ganglion Cells and PC12 Cells Requires Activity of CK1δ and CK1ε Article Snippet: D4476 was applied using transfection reagent (Effectene, Qiagen, Hilden, Germany) as described previously . .. The cells were monitored for 4 h and phase contrast or bright field time-lapse recordings were taken under 40× magnification using the Olympus IX81 microscope (Olympus, Hamburg, Germany) and the Article Title: Stathmin Regulates Keratinocyte Proliferation and Migration during Cutaneous Regeneration Article Snippet: .. Cell migration was documented by time-lapse microscopy at 37°C, 5% CO 2 and 40% humidity using the Cell^R Imaging Station (Olympus, IX-81-ZDC microscope, C10600 ORCA-R 2 camera) every 20 to 60 min for 24 or 48 h. Samples were visualized using the following objectives: 10x UPLanF/, NA = 0.3, 20x UPLanSApo, NA =0.75, 40x UPLanSApo, NA = 0.95 (Olympus) and analysed by the Migration:Article Title: Stathmin Regulates Keratinocyte Proliferation and Migration during Cutaneous Regeneration Article Snippet: .. Cell migration was documented by time-lapse microscopy at 37°C, 5% CO 2 and 40% humidity using the Cell^R Imaging Station (Olympus, IX-81-ZDC microscope, C10600 ORCA-R 2 camera) every 20 to 60 min for 24 or 48 h. Samples were visualized using the following objectives: 10x UPLanF/, NA = 0.3, 20x UPLanSApo, NA =0.75, 40x UPLanSApo, NA = 0.95 (Olympus) and analysed by the Time-lapse Microscopy:Article Title: Stathmin Regulates Keratinocyte Proliferation and Migration during Cutaneous Regeneration Article Snippet: .. Cell migration was documented by time-lapse microscopy at 37°C, 5% CO 2 and 40% humidity using the Cell^R Imaging Station (Olympus, IX-81-ZDC microscope, C10600 ORCA-R 2 camera) every 20 to 60 min for 24 or 48 h. Samples were visualized using the following objectives: 10x UPLanF/, NA = 0.3, 20x UPLanSApo, NA =0.75, 40x UPLanSApo, NA = 0.95 (Olympus) and analysed by the |