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Mechanistic duality of transcription factor function in phytochrome signaling

Plasma was rapidly separated from cellular components by centrifuging at 3300 g at 4C for 15 min

For hPrdx6 protein purification, the crude protein extract was passed through the Ni-NTA agarose column pre-equilibrated with binding buffer (20 mM Tris (pH 7.0), 50 mM NaCl, 10 mM Imidazole), followed by washing and elution using wash buffer (20 mM Tris (pH 7.0), 50 mM NaCl, 60 mM Imidazole) and elution buffer (20 mM Tris (pH 7.0), 50 mM NaCl, 500 mM Imidazole), respectively

Arachidonic acid: physiological roles and potential health benefitsa review