MRX utilizes a remote photonic coupling to interfere with specific molecular bonding in the body to create a temporary incapacitation of the opponents. (i.e, remotely inhibiting the ability of oxygen to bind to hemoglobin creating temporary hypoxia in the opposing force). This enables forces in possession of MRX to overcome opposition troops without loss of life. Also capable of penetrating bunkers and armored vehicles, rendering occupants unconscious. A variation of the coupling precis enables the MRX technology to break the bonds of explosive projectiles, mines and other offensive weapons. The combination of MRX based, non lethal anti-personnel weapons with anti-munitions technology has changed the face and strategies employed on the battlefield. MRX may also be deployed as an anti-offensive weapons system, capable of remote catalysis of liquid and solid fuels (jet fuel, solid fueled missiles, liquid fueled missiles, ICBM's, etc.) capable of nanosecond degradation of biological and chemical weapons. A variation of this technology can be used to remotely catalyze computer chips, rendering a jet, ICBM, tank, SAM ...etc., without electronics.....therefore useless. MRX defense is capable of limiting the damage to non permanent conditions. From lock on to triggering is 45 nanoseconds.
Controlled duration and degree of pain Pinpoint accuracy or wide dispersal pattern achieved from ground, space, air and naval platforms.
Hemoglobin - prevents oxygen from binding to hemoglobin, effect of suffocation, intensity of effect dependent on duration of scan.
Dopamine-blocks binding of dopamine to the receptor site; complete paralysis, reversible if beam intensity is below lethal threshold. Endorphin, dynorphin, enkephalin - blocks receptor binding, immediate symptoms of pain, diarrhea, nausea, fatigue, reversible. Cardiac-remote inducement of cardiac arrhythmias or failure.