? 手動操作微定位器，**控制初始預張力 ? 可與微電*連接測量膜電位 ? 易與成像系統(tǒng)連接，測量張力的同時進行血管壁熒光分析 ? 血管標準化模塊自動計算血管初始預張力
FEATURES & BENEFITS Manually operated micropositioner for accurate tension control Can be easily combined with microelectrodes for membrane potential measurements Easily integrated into an imaging system for simultaneous force measurements and vessel wall fluorescence Digital output. Data directly piped into Labchart Pro The Single Wire Myograph System - 320A is ideal for studying a single vessel with a diameter of 30 μm - 3 mm. The vessel is mounted as a ring preparation by threading it over two parallel stainless steel wires and securing the wires to two supports or "jaws". One support is attached to a precision micrometer, allowing manual control of vessel circumference and stretch. The other support is attached to a force transducer for measurements of force/tension development. The preparation is mounted in a heated 10 ml acid-resistant, stainless steel chamber, which can be covered with a lid featuring ports for rapid suction/draining, refilling and bubbling of oxygen. The base of the chamber contains a window allowing morphological observation or fluorescence measurements on an inverted microscope. Typically, the preparation is kept in the heated vessel chamber in a physiological salt solution at 37°C, bubbled with oxygen where the vessels remain viable for at least 12 hours.
The Single Wire Myograph System - 320A is ideal for studying a single vessel with a diameter of 60 μm - 3 mm. The vessel is mounted as a ring preparation by threading it over two parallel stainless steel wires and securing the wires to two supports or "jaws". One support is attached to a precision micrometer, allowing manual control of vessel circumference and stretch. The other support is attached to a force transducer for measurements of force/tension development. The preparation is mounted in a heated 10 ml acid-resistant, stainless steel chamber, which can be covered with a lid featuring ports for rapid suction/draining, refilling and bubbling of oxygen. The base of the chamber contains a window allowing morphological observation or fluorescence measurements on an inverted microscope. Typically, the preparation is kept in the heated vessel chamber in a physiological salt solution at 37°C, bubbled with oxygen where the vessels remain viable for at least 12 hours.