fitc labeled phalloidin (Beijing Solarbio Science)
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Fitc Labeled Phalloidin, supplied by Beijing Solarbio Science, used in various techniques. Bioz Stars score: 96/100, based on 585 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/phalloidin+fitc/FITC+Phalloidin/pmc13091063-315-21-37
Average 96 stars, based on 585 article reviews
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Incubation:Article Title: An Intelligent Magneto‐Mechanical Platform for Cellular Sensing in 3D Microenvironments Article Snippet: .. In order to label the filamentous actin (F‐actin), we incubated the cells with 1 μg/mL Article Title: Targeting JAK2 with a multifunctional nanoinhibitor for long-lasting anti-inflammatory effects and bone repair. Article Snippet: Following this period, the cells were fixed with 4% paraformaldehyde for 10 min and permeabilized with 0.1% Triton X-100 for 10 min. Nonspecific binding sites were blocked with 5% goat serum for 1 h. Subsequently, cells were incubated overnight at 4 °C with anti-OCN (23418-1-AP, 1:400, Proteintech). .. The next day, cells were incubated with CoraLite594-conjugated secondary antibody (SA00013-4, 1:200, Proteintech) and Article Title: Finerenone ameliorates high-fat-induced myocardial lipotoxicity by suppressing ferroptosis through augmenting the system Xc - /GSH synthesis pathway. Article Snippet: Obesity cardiomyopathy (OCM) is a distinct clinical entity in cardiovascular disease, yet targeted therapeutic options are scarce.. Finerenone, a novel nonsteroidal mineralocorticoid receptor antagonist, has shown cardioprotective effects, but its role in mitigating OCM lipotoxicity is unclear.. To elucidate the underlying functions and mechanisms, rats were fed on an HFD for 16 weeks to establish the OCM model. At the 12th week of HFD, the OCM rats were administered 10 mg/kg finerenone for 4 weeks. Article Title: Targeting JAK2 with a multifunctional nanoinhibitor for long-lasting anti-inflammatory effects and bone repair Article Snippet: Following this period, the cells were fixed with 4% paraformaldehyde for 10 min and permeabilized with 0.1% Triton X-100 for 10 min. Nonspecific binding sites were blocked with 5% goat serum for 1 h. Subsequently, cells were incubated overnight at 4 °C with anti-OCN (23418-1-AP, 1:400, Proteintech). .. The next day, cells were incubated with CoraLite594-conjugated secondary antibody (SA00013-4, 1:200, Proteintech) and Article Title: An Intelligent Magneto-Mechanical Platform for Cellular Sensing in 3D Microenvironments. Article Snippet: .. In order to label the filamentous actin (F-actin), we incubated the cells with 1 μg/mL Labeling:Article Title: An Intelligent Magneto‐Mechanical Platform for Cellular Sensing in 3D Microenvironments Article Snippet: .. In order to label the filamentous actin (F‐actin), we incubated the cells with 1 μg/mL Article Title: An Intelligent Magneto-Mechanical Platform for Cellular Sensing in 3D Microenvironments. Article Snippet: .. In order to label the filamentous actin (F-actin), we incubated the cells with 1 μg/mL Microscopy:Article Title: An Intelligent Magneto‐Mechanical Platform for Cellular Sensing in 3D Microenvironments Article Snippet: .. In order to label the filamentous actin (F‐actin), we incubated the cells with 1 μg/mL Article Title: An Intelligent Magneto-Mechanical Platform for Cellular Sensing in 3D Microenvironments. Article Snippet: .. In order to label the filamentous actin (F-actin), we incubated the cells with 1 μg/mL Confocal Laser Scanning Microscopy:Article Title: Targeting JAK2 with a multifunctional nanoinhibitor for long-lasting anti-inflammatory effects and bone repair. Article Snippet: Following this period, the cells were fixed with 4% paraformaldehyde for 10 min and permeabilized with 0.1% Triton X-100 for 10 min. Nonspecific binding sites were blocked with 5% goat serum for 1 h. Subsequently, cells were incubated overnight at 4 °C with anti-OCN (23418-1-AP, 1:400, Proteintech). .. The next day, cells were incubated with CoraLite594-conjugated secondary antibody (SA00013-4, 1:200, Proteintech) and Article Title: Targeting JAK2 with a multifunctional nanoinhibitor for long-lasting anti-inflammatory effects and bone repair Article Snippet: Following this period, the cells were fixed with 4% paraformaldehyde for 10 min and permeabilized with 0.1% Triton X-100 for 10 min. Nonspecific binding sites were blocked with 5% goat serum for 1 h. Subsequently, cells were incubated overnight at 4 °C with anti-OCN (23418-1-AP, 1:400, Proteintech). .. The next day, cells were incubated with CoraLite594-conjugated secondary antibody (SA00013-4, 1:200, Proteintech) and Staining:Article Title: Loss of <scp>SMN</scp> Impairs Osteoblast–Osteoclast Coupling via <scp>IGF1</scp>–Akt–<scp>OPG</scp> Axis in Spinal Muscular Atrophy Article Snippet: Multinucleated osteoclasts were identified using TRAP staining (Sigma- Aldrich, 387A) according to the manufacturer's instructions. .. For cytoskeleton visualization, cells were stained with Article Title: Finerenone ameliorates high-fat-induced myocardial lipotoxicity by suppressing ferroptosis through augmenting the system Xc - /GSH synthesis pathway. Article Snippet: Obesity cardiomyopathy (OCM) is a distinct clinical entity in cardiovascular disease, yet targeted therapeutic options are scarce.. Finerenone, a novel nonsteroidal mineralocorticoid receptor antagonist, has shown cardioprotective effects, but its role in mitigating OCM lipotoxicity is unclear.. To elucidate the underlying functions and mechanisms, rats were fed on an HFD for 16 weeks to establish the OCM model. At the 12th week of HFD, the OCM rats were administered 10 mg/kg finerenone for 4 weeks. Article Title: Loss of SMN Impairs Osteoblast–Osteoclast Coupling via IGF1 –Akt– OPG Axis in Spinal Muscular Atrophy Article Snippet: Multinucleated osteoclasts were identified using TRAP staining (Sigma‐Aldrich, 387A) according to the manufacturer's instructions. .. For cytoskeleton visualization, cells were stained with Article Title: Optimized Design of a Magnetic-Controlled Transportation Tool for Directional Cell Migration. Article Snippet: To address the challenge of efficiently guiding directional cell migration, this study optimizes the design of a magnetically controlled transportation tool for cell migration.. The magnetic carriers are fabricated using digital light processing, with biocompatibility, magnetic particle dispersion, mechanical properties, magnetism, and printability serving as the selection criteria.. Based on these evaluations, a base material and a magnetic particle content of 30 wt.% are determined. |
