fx-4000tt system (Flexcell International Corp)
90
Structured Review
Flexcell International Corp
fx-4000tt system
Fx 4000tt System, supplied by Flexcell International 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/fx-4000tt+system/fx+4000tm+tension+system/10__1007_slash_s13206___015___9201___8-161-20-22
Average 90 stars, based on 1 article reviews
Fx 4000tt System, supplied by Flexcell International 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/fx-4000tt+system/fx+4000tm+tension+system/10__1007_slash_s13206___015___9201___8-161-20-22
Average 90 stars, based on 1 article reviews
fx-4000tt system - by Bioz Stars,
2026-09
90/100 stars
Images
Related Articles
Construct:Article Title: Implantable thin-film porous microelectrode array (P-MEA) for electrical stimulation of engineered cardiac tissues Article Snippet: We have designed, fabricated, and validated a novel porous, multielectrode array (P-MEA) device capable of low-voltage electrical stimulation of engineered cardiac tissues (ECTs).. The primary advantage of this device is the ability to successfully function at a very low voltage thus minimizing any undesirable oxidative by-products in the culture environment or cell injury.. Major features of our P-MEA include dimensions of 10 mm width and 82 mm length, four arms to allow movement of the individual pads within ECTs, each embedded electrode arm incorporates eight 100 μm×200 μm rectangular pores surrounding a 950μm×340μm exposed electrode, large pads on either side of the porous embedded device to function as current return electrodes, suture holes to aid in vivo suturing and stabilization, and an eight electrode connector pads. Article Title: Engineered early embryonic cardiac tissue retains proliferative and contractile properties of developing embryonic myocardium. Article Snippet: Kimimasa Tobita, Li J. Liu, Andrzej M. Janczewski, Joseph P. Tinney, Jill M. Nonemaker, Serena Augustine, Donna B. Stolz, Sanjeev G. Shroff, and Bradley B. Keller Cardiovascular Development Research Program, Children’s Hospital of Pittsburgh of University of Pittsburgh Medical Center, and Department of Pediatrics, University of Pittsburgh School of Medicine; and Departments of Bioengineering and of Physiology and Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania Article Title: Engineered Early Embryonic Cardiac Tissue Increases Cardiomyocyte Proliferation by Cyclic Mechanical Stretch via p38-MAP Kinase Phosphorylation Article Snippet: Cylindrical-shaped EEECTs were constructed using Membrane:Article Title: Implantable thin-film porous microelectrode array (P-MEA) for electrical stimulation of engineered cardiac tissues Article Snippet: We have designed, fabricated, and validated a novel porous, multielectrode array (P-MEA) device capable of low-voltage electrical stimulation of engineered cardiac tissues (ECTs).. The primary advantage of this device is the ability to successfully function at a very low voltage thus minimizing any undesirable oxidative by-products in the culture environment or cell injury.. Major features of our P-MEA include dimensions of 10 mm width and 82 mm length, four arms to allow movement of the individual pads within ECTs, each embedded electrode arm incorporates eight 100 μm×200 μm rectangular pores surrounding a 950μm×340μm exposed electrode, large pads on either side of the porous embedded device to function as current return electrodes, suture holes to aid in vivo suturing and stabilization, and an eight electrode connector pads. Article Title: Engineered early embryonic cardiac tissue retains proliferative and contractile properties of developing embryonic myocardium. Article Snippet: Kimimasa Tobita, Li J. Liu, Andrzej M. Janczewski, Joseph P. Tinney, Jill M. Nonemaker, Serena Augustine, Donna B. Stolz, Sanjeev G. Shroff, and Bradley B. Keller Cardiovascular Development Research Program, Children’s Hospital of Pittsburgh of University of Pittsburgh Medical Center, and Department of Pediatrics, University of Pittsburgh School of Medicine; and Departments of Bioengineering and of Physiology and Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania Article Title: Engineered Early Embryonic Cardiac Tissue Increases Cardiomyocyte Proliferation by Cyclic Mechanical Stretch via p38-MAP Kinase Phosphorylation Article Snippet: Cylindrical-shaped EEECTs were constructed using Incubation:Article Title: Implantable thin-film porous microelectrode array (P-MEA) for electrical stimulation of engineered cardiac tissues Article Snippet: We have designed, fabricated, and validated a novel porous, multielectrode array (P-MEA) device capable of low-voltage electrical stimulation of engineered cardiac tissues (ECTs).. The primary advantage of this device is the ability to successfully function at a very low voltage thus minimizing any undesirable oxidative by-products in the culture environment or cell injury.. Major features of our P-MEA include dimensions of 10 mm width and 82 mm length, four arms to allow movement of the individual pads within ECTs, each embedded electrode arm incorporates eight 100 μm×200 μm rectangular pores surrounding a 950μm×340μm exposed electrode, large pads on either side of the porous embedded device to function as current return electrodes, suture holes to aid in vivo suturing and stabilization, and an eight electrode connector pads. Article Title: Engineered early embryonic cardiac tissue retains proliferative and contractile properties of developing embryonic myocardium. Article Snippet: Kimimasa Tobita, Li J. Liu, Andrzej M. Janczewski, Joseph P. Tinney, Jill M. Nonemaker, Serena Augustine, Donna B. Stolz, Sanjeev G. Shroff, and Bradley B. Keller Cardiovascular Development Research Program, Children’s Hospital of Pittsburgh of University of Pittsburgh Medical Center, and Department of Pediatrics, University of Pittsburgh School of Medicine; and Departments of Bioengineering and of Physiology and Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania Article Title: Engineered Early Embryonic Cardiac Tissue Increases Cardiomyocyte Proliferation by Cyclic Mechanical Stretch via p38-MAP Kinase Phosphorylation Article Snippet: Cylindrical-shaped EEECTs were constructed using |