De-staining Shaker FM-DS-A100

De-staining Shaker FM-DS-A100

De-staining Shaker FM-DS-A100 has microprocessor PID controlled system with LED display. Features orbital 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 20 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.

  •  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 Orbital
Shaking speed 30 to 300 rpm
Shaking accuracy ±1 rpm
Vibration range Φ 20 mm
Shaking tray size 320 × 300 mm
Program control 8 segments (adjustable)
Drive mode Single shaft drive
Display LED
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 395 × 300 × 200 mm
Net weight 15 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.