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Featured Products |
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Assay Kits for Mitochondrial Trifunctional Protein (MTP)
Inherited deficiency of MTP is a genetic disease which occurs in approximately 1:38,000 newborns in the US. Deficiency of LCHAD (the dehydrogenase part of MTP) has also been found in children of women who develop HELLP syndrome and AFLP syndrome, both of which are life-threatening obstetric conditions. Furthermore, heterozygous individuals for MTP defects are more susceptible to nonalcoholic hepatic steatosis, or nonalcoholic fatty liver disease (NAFLD), the most common form of liver disease in the US.
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News |
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April 15 - MitoSciences and the University of Oregon announce exclusive biotechnology transfer agreement. Click here for the complete press release.
April 9 - MitoSciences and Invitrogen announce distribution and co-development agreement. Click here for the complete press release.
March 16 - MitoSciences has launched the MitoTox™ line of products and services for mitochondrial toxicity screening. MitoTox™ offers the most complete set of
solutions for understanding drug-induced mechanisms of mitochondrial inhibition.
Company news archive
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