APLP-2 Polyclonal Antibody, 100ul NGS Oligos Defects in this gene are

Defects in this gene are associated with osteogenesis imperfecta| a connective tissue disorder characterized by bone fragility and low bone mass

Contains 2 B box-type zinc fingers

in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies

The head structure formed by these 2 proteins on one end of the titin string extends into the center of the M band

Diseases associated with GPR68 include ovarian cancer

APLP-2 Polyclonal Antibody, 100ul NGS Oligos Defects in this gene areAPLP2 encodes amyloid precursor like protein 2 (APLP2), which is a member of the APP (amyloid precursor protein) family including APP, APLP1 and APLP2. Amyloid like protein 2 is ubiquitously expressed. It contains heparin , copper and zinc binding domains at the N terminus, BPTI Kunitz inhibitor and E2 domains in the middle region, and transmembrane and intracellular domains at the C terminus. This protein interacts with major histocompatibility