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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)

The E2F proteins contain several evolutionarily conserved domains that are present in most members of the family

After washing to remove unbound substances

which is proposed to function as a trans-acting regulatory RNA

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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