HLX1 Polyclonal Antibody, 100ul Centrifuge Tube (Bottle) Mutations in ELOVL5 have been

Mutations in ELOVL5 have been associated with spinocerebellar ataxia-38 (SCA38)

The encoded protein interacts with the mitochondrial calcium uniporter

• Maximum capacity 50mL ×4

This gene is a member of the alpha interferon gene cluster on the short arm of chromosome 9

HLX1 Polyclonal Antibody, 100ul Centrifuge Tube (Bottle) Mutations in ELOVL5 have beenHLX is a Protein Coding gene. H2. 0 Like Homeobox is a transcription factor required for TBX21 T bet dependent maturation of Th1 cells as well as maintenance of Th1 specific gene expression. Involved in embryogenesis and hematopoiesis Diseases associated with HLX include ovarian endodermal sinus tumor and ovarian primitive germ cell tumor. Among its related pathways are IL12 mediated signaling events. Gene Ontology (GO) annotations related to HLX