ApoL5 Polyclonal Antibody, 50ul Cell Labeling & Imaging Defects in this gene may

Defects in this gene may underlie brain disorders such as schizophrenia and epilepsy

where its primary property is to respond to the pituitary hormone arginine vasopressin (AVP) by stimulating mechanisms that concentrate the urine and maintain water homeostasis in the organism

Monomer and component of the SFPQ-NONO complex

Deprivation of BCAS2 through RNA inhibition induces apoptosis in p53-wild type cells

A pseudogene of this gene is located on the long arm of chromosome 14

ApoL5 Polyclonal Antibody, 50ul Cell Labeling & Imaging Defects in this gene mayAPOL5 (apolipoprotein L5) is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles.