EFGM Polyclonal Antibody, 20ul Syringe Filter Mutations in this gene are

Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease)

This receptor has been shown to stimulate NF-kappa B activity and regulate cell apoptosis

this protein is essential for chromosome alignment at the centromere during mitosis and is required for centrosome duplication

This gene encodes a dual-function 65 kDa protein that undergoes proteolytic cleavage to produce a 45 kDa N-terminal fragment with a paired-like homeodomain and a 20 kDa C-terminal fragment with a proline-rich domain

The protein encoded by this gene is an inositol 1

EFGM Polyclonal Antibody, 20ul Syringe Filter Mutations in this gene areEukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors. Its role in the regulation of normal