OXA1L Rabbit Polyclonal Antibody, 20ul Custom DNA Oligos Defects in this gene are

Defects in this gene are a cause of susceptibility to familial hypertrigliceridemia

This protein may be involved in the assembly and stabilization of actin-filaments and likely plays a role in modulating cell adhesion| cell morphology and cell motility

you can confidently detect IL-10 levels in 48 tests

|tissue specificity:Expressed in umbilical vein endothelial cells and several cancer cell lines (at protein level)

IP6K3 encodes a protein that belongs to the inositol phosphokinase (IPK) family

OXA1L Rabbit Polyclonal Antibody, 20ul Custom DNA Oligos Defects in this gene areThis gene encodes an evolutionarily conserved protein that is localized to the inner mitochondrial membrane. The encoded protein is essential for the translocation of the N terminal tail of subunit 2 of cytochrome c oxidase and is involved in the assembly of the cytochrome c oxidase and ATPase complexes of the mitochondrial respiratory chain.