ALDH1A1 Polyclonal Antibody, 50ul Mechanical Pipette Certain mutations in this gene

Certain mutations in this gene resulting in a functionally inadequate enzyme are associated with a rare genetic disorder causing nonspherocytic hemolytic anemia

the interaction promotes erythropoiesis

where it binds OGF and is translocated into the nucleus

and is similar to several known polo-like kinase kinases

q23) translocation involving this gene has also been identified

ALDH1A1 Polyclonal Antibody, 50ul Mechanical Pipette Certain mutations in this geneRetinal dehydrogenase 1 encoded by ALDH1A1 belongs to the aldehyde dehydrogenase family. Aldehyde dehydrogenase is the next enzyme after alcohol dehydrogenase in the major pathway of alcohol metabolism. There are two major aldehyde dehydrogenase isozymes in the liver, cytosolic and mitochondrial, which are encoded by distinct genes, and can be distinguished by their electrophoretic mobility, kinetic properties, and subcellular localization. This gene