sa3800 software (Sony)
90
Structured Review
Sony
sa3800 software
Sa3800 Software, supplied by Sony, 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/through-flow+computer+program/sh800+cell+sorter/pm36597025-84-15-14
Average 90 stars, based on 1 article reviews
Sa3800 Software, supplied by Sony, 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/through-flow+computer+program/sh800+cell+sorter/pm36597025-84-15-14
Average 90 stars, based on 1 article reviews
sa3800 software - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: RNA activation of CEBPA improves leukemia treatment Article Snippet: The samples were then stained for human CD45 marker (Brilliant Violet 421, mouse, monoclonal, 1:100, BioLegend, clone HI30) and analyzed using the Sony ID7000 full-spectrum flow cytometer. Article Title: Human neural stem cell–derived extracellular vesicles protect against ischemic stroke by activating the PI3K/AKT/mTOR pathway Article Snippet: Stained cells were detected and sorted by flow cytometry (Sony, Tokyo, Japan, SH800), and the fluorescence intensity was statistically analyzed. Flow Cytometry:Article Title: RNA activation of CEBPA improves leukemia treatment Article Snippet: Cells were harvested as described above, washed twice with 2% FBS/PBS, and stained with the LIVE/DEAD fixable green dead cell stain kit (Thermo Fisher Scientific) according to the manufacturer’s instructions. .. Samples were analyzed using the Sony Article Title: RNA activation of CEBPA improves leukemia treatment Article Snippet: Cells were then collected, washed twice with PBS, and stained for live and dead cells with the LIVE/DEAD fixable green dead cell stain kit (Thermo Fisher Scientific) according to the manufacturer’s instructions. .. Flow cytometry analysis was then performed on samples using the Sony Fluorescence:Article Title: RNA activation of CEBPA improves leukemia treatment Article Snippet: Cells were harvested as described above, washed twice with 2% FBS/PBS, and stained with the LIVE/DEAD fixable green dead cell stain kit (Thermo Fisher Scientific) according to the manufacturer’s instructions. .. Samples were analyzed using the Sony Article Title: Development of a novel anti-human glypican 5 monoclonal antibody (G 5 Mab-1) for multiple applications Article Snippet: .. Afterward, cells were treated with Alexa Fluor 488-conjugated anti-mouse IgG (1:1000) following the collection of fluorescence data using the Software:Article Title: RNA activation of CEBPA improves leukemia treatment Article Snippet: Cells were harvested as described above, washed twice with 2% FBS/PBS, and stained with the LIVE/DEAD fixable green dead cell stain kit (Thermo Fisher Scientific) according to the manufacturer’s instructions. .. Samples were analyzed using the Sony Stable Transfection:Article Title: Development of a novel anti-human glypican 5 monoclonal antibody (G 5 Mab-1) for multiple applications Article Snippet: The expression plasmid of human GPC5 was subcloned into a pCAG-ble vector (FUJIFILM Wako Pure Chemical Corporation, Osaka, Japan). pCAG-hGPC5 vector was transfected into cell lines using the Neon transfection system (Thermo Fisher Scientific, Inc., Waltham, MA, USA). .. Subsequently, LN229 and CHO–K1, which stably overexpressed GPC5 (hereafter described as LN229/GPC5 and CHO/GPC5, respectively), were stained with an anti-GPC5 mAb (clone 297716; R&D Systems, Inc., Minneapolis, MN, USA) and sorted using the Staining:Article Title: Development of a novel anti-human glypican 5 monoclonal antibody (G 5 Mab-1) for multiple applications Article Snippet: The expression plasmid of human GPC5 was subcloned into a pCAG-ble vector (FUJIFILM Wako Pure Chemical Corporation, Osaka, Japan). pCAG-hGPC5 vector was transfected into cell lines using the Neon transfection system (Thermo Fisher Scientific, Inc., Waltham, MA, USA). .. Subsequently, LN229 and CHO–K1, which stably overexpressed GPC5 (hereafter described as LN229/GPC5 and CHO/GPC5, respectively), were stained with an anti-GPC5 mAb (clone 297716; R&D Systems, Inc., Minneapolis, MN, USA) and sorted using the |