Aldolase B Polyclonal Antibody, 50ul Peptide Synthesis 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

There are 3 distinct domains of this factor: extracellular

Mammalian mitochondrial ribosomal protein L 16 (39S ribosomal protein L16 mitochondrial) is encoded by nuclear gene MRPL16 and help in protein synthesis within the mitochondrion

The encoded protein has homology with other proteins that function as cell-adhesion molecules or as signal transduction receptors and is a candidate for the target gene in the 1q32

This kinase has been shown to specifically activate MAPK8/JNK

Aldolase B Polyclonal Antibody, 50ul Peptide Synthesis Mutations in this gene causeFructose 1,6 bisphosphate aldolase (EC 4. 1. 2. 13) is a tetrameric glycolytic enzyme that catalyzes the reversible conversion of fructose 1,6 bisphosphate to glyceraldehyde 3 phosphate and dihydroxyacetone phosphate. Vertebrates have 3 aldolase isozymes which are distinguished by their electrophoretic and catalytic properties. Differences indicate that aldolases A, B, and C are distinct proteins, the products of a family of related 'housekeeping'