MRP-L40 Polyclonal Antibody, 20ul Culture Media 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)

CLPTM1 (Cleft Lip And Palate Associated Transmembrane Protein 1) is a Protein Coding gene

PRKAG2 (protein kinase AMP-activated non-catalytic subunit gamma 2) is a member of the AMPK gamma subunit family

checkpoint proteins RAD17 and RAD9

Clinical studies suggest this gene as a candidate gene for the insulin resistance syndrome

MRP-L40 Polyclonal Antibody, 20ul Culture Media Mutations in this gene areMammalian mitochondrial ribosomal protein L 40 (39S ribosomal protein L40 mitochondrial) is encoded by nuclear gene MRPL40 and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and