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Power and versatility
The Bio-Link crosslinker is a complete, microprocessor
controlled UV irradiation system, mainly dedicated
to the linking of nucleic acid to membranes
and elimination of PCR contamination. Its innovative
design ensures unique features:
Microprocessor controlled
The programmable microprocessor constantly monitor
the UV light emission. The irradiation stops
automatically when the energy received matches
the programmed energy.
Reproducibility
Thanks to its UV sensors, irradiation cycles
are perfectly reproducible, regardless of intensity
fluctuation of the UV source. Just programme
your energy and Bio-Link delivers it !
Durability
Bio-Link combines the latest technology with
a very high quality of components : UV exposure
chamber in stainless steel, protective quartz
disk on the UV sensor cell, highly resistant
tactile membrane keypad.
Ease of use
The readout display and the large number of
presets, in either energy unit (Joules/cm²)
or time unit (seconds) makes the Bio-Link a
very simple instrument to use while very powerful.
Consistent measure
The UV light intensity is captured in a well
of light, positioned above the irradiation chamber.
The UV cell measure is then collected from all
the UV tubes and not jut one. This also protect
the UV cell from any dirt which can enter the
chamber.
:: Key features ::
Microprocessor control
:: Precise irradiation in either energy (Joules/cm²)
or time (seconds)
:: Preset programme for dosage of 0.120 J/cm²
to
optimised nucleic acid immobilisation
:: 9 preset programmes for UV energy exposure
:: 9 preset programmes for time exposure
:: Manual setting of UV energy or time exposure
:: Storage of the last UV setting
:: Tactile membrane keypad
:: Large L.E.D. readout
:: 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
:: Applications
:: Crosslinking of DNA and RNA to nylon or
nitrocellulose membranes for
blots
:: Nicking of ethidium bomide stained DNA in
agarose gels
:: RecA mutation screening
:: Elimination of PCR contamination
:: UV sterilisation
:: UV curing of polymers
:: Gene mapping for creating cleavage-inhibiting
thymine dimers