AL4A1 Rabbit Polyclonal Antibody, 100ul Shakers This powerful solution offers 200

This powerful solution offers 200 rxns per bottle at 1 rxn/μl

Humans have multiple PtdIns proteins that differ by the degree and position of phosphorylation of the inositol ring

PRPF31 encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes

COL4A3 is also linked to an autosomal recessive form of Alport syndrome

AL4A1 Rabbit Polyclonal Antibody, 100ul Shakers This powerful solution offers 200This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline 5 carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta 1 pyrroline 5 carboxylate (P5C) and proline. Alternatively