CMC2 Polyclonal Antibody, 50ul sgRNA Oligos Deficiencies of MBL2 have been

Deficiencies of MBL2 have been associated with susceptibility to autoimmune and infectious diseases

The D4Z4 repeat is polymorphic in length and a similar D4Z4 repeat array has been identified on chromosome 10

as represented in GeneID: 106780802

Another family of proteins

the protein localizes to centrosomes in association with gamma-tubulin

CMC2 Polyclonal Antibody, 50ul sgRNA Oligos Deficiencies of MBL2 have beenThis 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