APLP-2 Polyclonal Antibody, 20ul PCR Series Isoforms that are expressed in

Isoforms that are expressed in muscle and ubiquitously expressed isoforms localize to the cytoplasm and nucleus and activate a caspase-independent apoptotic process

catalyzes the conversion of arachidonic acid to 5(S)-hydroperoxy-6-trans-8

The tilted bottleneck facilitates easy access of pipets and cell scrapers

Mutations in DCLRE1C can cause Athabascan-type severe combined immunodeficiency (SCIDA) and Omenn syndrome

APLP-2 Polyclonal Antibody, 20ul PCR Series Isoforms that are expressed inAPLP2 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