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The H protein then shuttles this methylamine group to the T protein, which catalyzes the transfer of the methylene group (CH 2 ) to tetrahydrofolate, forming 5,10-methylenetetrahydrofolate
The clinically normal heterozygous carriers for this disease have about half of the normal glutathione synthetase activity, as predicted, but have normal clinical phenotypes, cellular glutathione levels, and 5-oxoproline excretion (53)
This product is intended strictly for laboratory research purposes and is not for human consumption, clinical, diagnostic, or therapeutic use
However, oral Glutathione has limited bioavailability, meaning only a portion gets absorbed through digestion
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