HPS5 Polyclonal Antibody, 20ul Gel & Buffers leads to the genetic disorder

leads to the genetic disorder α1-antitrypsin deficiency

It functions as a pattern-recognition receptor that recognizes a variety of beta-1

This gene encodes antizyme 3

The encoded protein plays a role in eye development

This protein also associates with centromeres in G2 phase

HPS5 Polyclonal Antibody, 20ul Gel & Buffers leads to the genetic disorderThis gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky Pudlak syndrome 6 protein and may interact with the cytoplasmic domain of integrin, alpha 3. Mutations in this gene are associated with Hermansky Pudlak syndrome type 5. Multiple transcript variants encoding two distinct isoforms have been identified for this gene.