Bio-Link 312

UV crosslinker for mediumwave UV light (312 nm).

Microprocessor-controlled UV irradiation system.


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Description
Your benefits


The emission of the UV light is constantly monitored by a UV sensor which is controlled by a microprocessor. The irradiation stops automatically when the energy received matches the energy programmed. The irradiation cycler are perfectly reproducible and are independent from intensity fluctuations of the UV source. Just programme the energy and Bio-Link delivers it! Bio-Link combines the latest technology with a very high quality of the components. UV exposure chamber in stainless steel, protective quartz disk on the UV sensor cell, highly resistant tactile membrane keypad. The readout display and the large number of presets, either in energy unit (Joules/cm²) or in time unit (seconds), makes the Bio-Link a very simple instrument to use while very powerful. The UV light intensity is captured in a well of light above the irradiation chamber, so that the UV cell measure is collected from all the UV tubes and not just one. This also protect the UV cell from any dirt which can enter the chamber


  • Microprocessor control
  • Precise irradiation either in energy (Joules/cm²) or in time (seconds)
  • Preset program for doses of 0.120 J/cm² for optimal nucleic acid immobilisation
  • 9 preset programs for UV energy exposure
  • 9 preset programs for time exposure
  • Manual setting of UV energy or time exposure
  • Storage of the last UV setting
  • Tactile membrane keypad
  • Large LED display
  • Protective quartz disk on the UV sensor cell
  • Spacious UV exposure chamber in stainless steel
  • Safety interlock door with UV blocking observation window
  • Automatic restart with no loss of information if breaking-off of circuit
  • Dual safety fuses
  • UV wavelength interchangeability (254 nm, 312 nm oder 365 nm)
  • Applications:
  • Crosslinking of DNA and RNA to nylon or nitrocellulose membranes for Southern, Northern, Dot and Slot blots
  • Nicking of ethidium bomide stained DNA in agarose gels
  • Partial endonuclease digest by formation of cleavage-inhibiting thymine dimers (gene mapping)
  • RecA mutation screening
  • Elimination of PCR contamination
  • UV sterilisation
  • UV curing of polymers

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