MICU1 Monoclonal Antibody(Mix), 20ul Site-directed Mutagenesis The ZEROTIP®Super Low Retention Tips

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an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation

MMP3 is part of a cluster of MMP genes which localize to chromosome 11q22

AMPK is activated

This protease forms a complex with the Kunitz-type serine protease inhibitor

MICU1 Monoclonal Antibody(Mix), 20ul Site-directed Mutagenesis The ZEROTIP®Super Low Retention TipsThis gene encodes an essential regulator of mitochondrial Ca2+ uptake under basal conditions. The encoded protein interacts with the mitochondrial calcium uniporter, a mitochondrial inner membrane Ca2+ channel, and is essential in preventing mitochondrial Ca2+ overload, which can cause excessive production of reactive oxygen species and cell stress. Alternatively spliced transcript variants encoding different isoforms have been described.