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CMC2 Polyclonal Antibody, 100ul Custom Peptide Synthesis Mutations in this gene are

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CMC2 Polyclonal Antibody, 100ul Custom Peptide Synthesis Mutations in this gene areThis gene is a member of the mitochondrial carrier family. The encoded protein contains four EF hand Ca(2+) binding motifs in the N terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple

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Description

Mutations in this gene are associated with autosomal recessive retinitis pigmentosa

ME2 encodes a mitochondrial NAD-dependent malic enzyme

and is found to be upregulated in multiple cancer cell lines

The protein has broad-spectrum antimicrobial activity against bacteria and fungi

It is a tetramer made up of alpha-beta dimers linked in a head-to-head arrangement

CMC2 Polyclonal Antibody, 100ul Custom Peptide Synthesis Mutations in this gene areThis gene is a member of the mitochondrial carrier family. The encoded protein contains four EF hand Ca(2+) binding motifs in the N terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple

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