De-staining Shaker FM-DS-A102

Name: De-staining Shaker FM-DS-A102
Brand: Fison
SKU: FM-DS-A102
Rating: 4.4 (201 reviews)

De-staining Shaker FM-DS-A102 has microprocessor PID control system with LCD display. Features linear oscillation mode, single shaft balance drive, 8 segment adjustable program controller and independent over speed acoustic and visual alarm. It comes with shaking speed range of 30 to 300 rpm and 25 mm vibration range. Designed with ABS plastic body and stainless steel tray. The unique design of speed monitoring circuit provides long working life under repeated and continuous use. Used for different applications of electrophoresis gel, dyeing or de-staining of coomassie blue, dyeing and development of silver nitrate and X-ray negative film, disposal of cellulose membrane after electrophoresis transfer, molecular hybridization and dyeing or cultivation of antigens and antibodies.

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✔ Microprocessor PID controlled system
✔ 8 segment adjustable program settings of different speed and time
✔ Single shaft drive technology
✔ Chrome alloy and iron casting key parts
✔ Recovery function after power cut-off
✔ Over speed acoustic and visual alarm function
✔ Slow start circuit prevent sudden start and liquid splash
✔ Power cut off protection for overheating motor and over temperature
✔ Frequency control system with accuracy ± 1 rpm
✔ Large torque converter motor

Controller	Microprocessor PID control system
Shaking mode	Linear
Shaking speed	30 to 300 rpm
Shaking accuracy	±1 rpm
Vibration range	Φ 25 mm
Shaking tray size	500 × 400 mm
Program control	8 segments (adjustable)
Drive mode	Single shaft drive
Display	LCD
Timing range	0 to 999.59 h (continuous)
Shaking plate quantity	1 pc
Tray material	Stainless steel tray
External material	ABS plastic
Safety function	Acoustic and visual alarm for over speed
Power	60 W
Power supply	AC 200 to 240 , 50 to 60 Hz
Dimension	550 × 480 × 280 mm
Net weight	40 kg

Used for different applications of electrophoresis gel, dyeing or de-staining of Coomassie blue, dyeing and development of silver nitrate and X-ray negative film, disposal of cellulose membrane after electrophoresis transfer, molecular hybridization and dyeing or cultivation of antigens and antibodies.