RM19 Polyclonal Antibody, 100ul Plates & Dishes Mutations in this gene cause

Mutations in this gene cause nephronophthisis (NPHP)| an autosomal recessive kidney disease characterized by tubular basement membrane disruption| interstitial lymphohistiocytic cell infiltration| and development of cysts at the corticomedullary border of the kidneys

Kit includes tunable VitroGel® YIGSR hydrogel with 12 x VitroPrime™® Cell Culture Inserts

are the force-generating proteins responsible for the sliding movement in axonemes

HP encodes a preproprotein

Plays an important role in the regulation of polyamine intracellular concentration and has the potential to act as a determinant of cellular sensitivity to the antitumor polyamine analogs

RM19 Polyclonal Antibody, 100ul Plates & Dishes Mutations in this gene causeMammalian mitochondrial ribosomal proteins are encoded by nuclear genes 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 prokaryotic ribosomes is that the latter contain a 5S