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Description
The coding region was cloned into a modified pETM-11 bacterial expression vector which was derived from a pET-24d(+) vector (Novagen) by insertion of a tobacco etch virus (TEV) protease cleavage site following an N terminal hexa-histidine and protein A tag
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No clinical trial has tested this combination, but the pharmacological logic supports the approach for researchers operating at the cutting edge
doi:10.1042/bj0860173
We are scientists! one of them exclaimed, looking at me like I was the mad scientist in the room
