德國sigma 2-7非冷凍臺式離心機,sigma 4000轉離心機 450 ml, 400 ml 4.000 min-1 2.540 x g臺式離心機、非冷藏、水平轉子、固定角轉子,PCR
450 ml, 400 ml
4.000 min-1
2.540 x g
臺式離心機、非冷藏、水平轉子、固定角轉子,PCR
德國sigma 2-7非冷凍臺式離心機,sigma 4000轉離心機 高性能,新設計
新的 Sigma 2-7 從客戶的體驗和希望中誕生。該離心機的技術特點令人印象深刻:不銹鋼碗、不平衡開關、機動蓋鎖、帶藍色 LED 的創新運行顯示和工藝可靠性。離心機在操作過程中也非常安靜。標本僅稍微加熱,這對于血液標本試管尤其重要。與多用途、模塊化的水平轉子配合使用,為用戶在許多實驗室成功的職業生涯奠定了基礎。
zui大速率 [min-1] | 4.000 |
---|---|
zui大相對離心力 [x g] | 2.540 |
zui大能力 [ml] | 30 x 15 ml, 4 x 100 ml |
工作溫度范圍 [°C] | |
節目 | 10 |
加速曲線 | 2 |
制動曲線 | 2 |
The Sigma 2-7 is equipped with a simple, clear display at the perfect viewing angle and large buttons for good legibility and easy operation. The uncomplicated Spincontrol E control unit makes data entry and programming simple. The centrifuge run time can be selected in seconds, and the LED indicator is readily visible at a distance. The most recent settings can be saved, and the standstill and run times are optionally programmable (e.g. clotting time). The motorised lid lock, which quietly closes automatically to eliminate extra effort, is a nice practical touch. With these features, the Sigma 2-7 stands for easy operation, convenience and maximum safety.
Sigma 2-7
Innovative LED running indicator, readily visible at a distance n Clearly organised display n Large buttons n Acoustic signal for button press and end of run n Motorised lid lock for easy, effortless operation n Low noise level – 55 dB(A) at maximum speed n Corrosion-resistant, easily cleaned stainless steel drum n Low height for easy loading and unloading n Automatic method for gel tubes n Settings can be modifi ed while running n Ten program memory slots n Low temperature rise in continuous operation n Zero-maintenance motor n Two acceleration and braking curves: soft and fast n Easy rotor exchange n Compact device; fi ts on every lab bench n Imbalance monitoring and shutdown n Overspeed monitoring n Window in lid for independent speed measurement n Manufactured in compliance with EN 61010-2-020 n RoHS compliant n Also available as IVD device conforming with Directive 98/79/EC regarding in-vitro diagnostic medical devices