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International Patent Pending) (dOdsample 340nm /min)/(dOdcontorl 340nm /min) x Control Value = Sample Value (Activity in U/g Hb) Odsample 405nm /ODcontrol 405nm wherein dODsample is the change in optical density (per minute) for the sample, 340nm is the wavelength at which optical density is measured under kinetic mode, dODcontrol is the change in optical density (per minute) of a control measured under kinetic mode conditions at a particular wavelength (340nm), ODsample is the optical density for the sample measured once at a particular wavelength (405nm), and ODcontrol is the optical density of the control measured once at that particular wavelength (405nm), 405nm is the wavelength at which a reading of Heamoglobin contained can be taken, the control value being determined by the change in optical density (per minute) of the control measured under kinetic mode at 340nm divided by the optical density of the control at 405nm i.e

[7] American chemist Edward Calvin Kendall was responsible for the isolation of thyroxine in 1915

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iGEM REPORT: Investigation of glutathione reductase and 25-hydroxylase for clearing aggregated proteins in an experimental fish eye cataract model Note : This iGEM Report was submitted to the PLOS iGEM Realtime Peer Review Jamboree, and has not undergone formal peer review by any of the PLOS journals