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LCN12 Rabbit Polyclonal Antibody, 100ul Digital Burette Defects in this gene are

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LCN12 Rabbit Polyclonal Antibody, 100ul Digital Burette Defects in this gene areMembers of the lipocalin family such as LCN12 have a common structure consisting of an 8 stranded antiparallel beta barrel that forms a cup shaped ligand binding pocket or calyx. Lipocalins generally bind small hydrophobic ligands and transport them to specific cells (Suzuki et al. 2004

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Description

Defects in this gene are a cause of branchiooculofacial syndrome (BOFS)

This gene encodes a calcium-binding protein

Mutations in this gene have been associated with pyruvate carboxylase deficiency

5-bisphosphate

After washing to remove unbound substances

LCN12 Rabbit Polyclonal Antibody, 100ul Digital Burette Defects in this gene areMembers of the lipocalin family such as LCN12 have a common structure consisting of an 8 stranded antiparallel beta barrel that forms a cup shaped ligand binding pocket or calyx. Lipocalins generally bind small hydrophobic ligands and transport them to specific cells (Suzuki et al. 2004

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