Abstract

During the first 24 hours after removal from incubation cultured B16-BL6 mouse melanoma cells displayed reliable increases in ultraweak photon emission (UPE) of specific wavelengths during discrete time portions of this 24 hour interval. The application of specific filters demonstrated reliable and clear increases in UPE dependent upon the wavelength being measured. Infrared (IR: 950 nm) and ultraviolet (UV: 370 nm) filters produced similar and protracted elevations in UPE that were offset by ∼3.5 hours (r=0.85). The IR wavelength produced UPE elevations 7 hours after removal from the incubator while the UV wavelength produced comparable increases 3.5 hours after the initial increase in IR. Wavelengths in the visible spectrum demonstrated increases in UPE roughly 20+ hours into testing. Precise activators and inhibitors for exact wavelengths were calculated based upon Cosic's Resonant Recognition Model (RRM) and produced either enhancement or diminishment of UPE only at the exact wavelength as predicted by the RRM. Other biochemical treatments predicted for other wavelengths, even those separated by 10 nm, were less or not effective. This 3.5 hour discrepancy between IR and UV emissions is consistent with the time frame between signaling molecules to growth and protein structural factors. This is of interest as signaling molecules are associated with IR while growth and structural proteins are associated with UV. This data lends support for a quantitative coupling between the wavelength of UPE and intrinsic cellular chemistry.Keywords: Ultraweak photon emissions (UPE) · Cosic Resonant Recognition Model · melanoma cells · near infrared · near ultraviolet.

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