Ultraviolet crosslinker UCL-3500

Brief Introduction:

The iqualitrol UV Crosslinker UCL-3500 is a high-power, complete, microprocessor-controlled UV irradiation system, mainly used to attach nucleic acids to membranes and eliminate PCR contamination.

The self-developed IQUALITROL programmable microprocessor continuously monitors the ultraviolet light emission.

The UCL-3500 ultraviolet crosslinking instrument is equipped with an aluminum alloy UV irradiation chamber and an aluminum diffuse reflection plate, and the irradiation intensity in the ultraviolet irradiation chamber is uniform.

The UV sensor located above the irradiation chamber is fitted with quartz glass to protect the sensor from chemical contamination.

Main Features:

Microprocessor Control: Programmable microprocessor monitors the intensity of UV light in real time. When the set energy is reached, the irradiation will stop immediately. There will be no energy impact due to the reduction of UV intensity caused by the aging of the lamp.

Uniformity: The irradiation room is made of stainless steel mirror and orange optical reflection plate. The ultraviolet sensor unit is located above the irradiation room and equipped with a quartz glass protective cover to ensure that the sensor is not polluted and durable.

Ease of use: It can be operated in multiple modes such as time mode, energy mode, and preset mode.

Fast: The default operation setting program before shutdown is entered after booting, one-key operation, convenient and fast.

Buzzer reminder: when the cross-linking is over, the buzzer will remind you, without any operation, it will automatically enter the standby state.

Simple operation: Microprocessor control, preset common programs, easy to operate!

Uniform illumination: The mirror reflector and the orange reflector are used together to ensure uniform light intensity throughout the irradiation room!

Application:

UV-induced mutation;

Eliminate PCR contamination and UV sterilization;

RecA mutation screening in Escherichia coli;

Membrane crosslinking of nucleic acids;

Biomolecular cross-linking;

DNA cleavage in agarose gel.