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By G. Renger (auth.), Jiin-Ju Chang, Joachim Fisch, Fritz-Albert Popp (eds.)

ISBN-10: 9048150337

ISBN-13: 9789048150335

ISBN-10: 9401709289

ISBN-13: 9789401709286

It is now good validated that each one residing platforms emit a vulnerable yet everlasting photon flux within the obvious and ultraviolet variety. This biophoton emission is correlated with many, if no longer all, organic and physiological capabilities. There are symptoms of a hitherto-overlooked info channel in the dwelling approach. Biophotons might set off chemical reactivity in cells, development keep watch over, differentiation and intercellular verbal exchange, i.e. organic rhythms. the fundamental experimental and theoretical framework, the technical difficulties and the extensive box of purposes within the meals undefined, medication, pharmacology, environmental technological know-how and simple sciences are awarded during this e-book, which additionally comprises the swiftly growing to be literature.
This booklet is written by means of the main impressive overseas scientists acquainted with this subject who've been operating during this box for plenty of years.

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2 EFFECT OF EXOGENOUS H 20 2 In order to investigate, whether the different intensities of the Efaecalis emission in different media are due to different amounts of H20 2 accumulated, we tested several media for their response on H20 2• We added different amounts ofH20 2 to M17, HNB and a minimal salts solution and measured the chemiluminescence of the sample for ten minutes immediately afterwards. Parallel, we measured the inhibition of the induced chemiluminescence upon addition of catalase at a concentration of 1000 sigma units/ml.

After incubation, each group of the sections was homogenized with 100 mL of chloroform-methanol (1: I vollv'ol). The homogenate was filtrated through a glass fiber filter (Advantec GA200) and the tissue residue was washed with 50 mL of extracting solvent. The filtrate was shaken with 50 mL of deionized water, and the suspension was centrifuged to separate it into two layers. The lower chloroform layer obtained was evaporated. The concentrate was dissolved in 2 mL of extraction solvent. Two hundred microliter portions of each extract were applied onto a silicagel plate (Whatman PK5) and developed with n-hexane-ethyl acetate (4: I vol/vol) for I h.

Condition I 2 3 4 5 6 7 8 Living Living Living Living Living Living Dead Dead Condition Living Living Living Living Dead Distd. 5 Time (h at peak counts) 10 13 22 ~24 ~24 0* 0* 0* *Experiment nos. 6-8 had no peaks in the ultraweak luminescence. c 51 50 '

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Biophotons by G. Renger (auth.), Jiin-Ju Chang, Joachim Fisch, Fritz-Albert Popp (eds.)

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