APLP-2 Polyclonal Antibody, 20ul PCR Series It's non-treated

It's non-treated

This autosomal dominant disorder is characterized by abnormal water reabsorption by kidney tubules due

When bound to KRT17

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

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

APLP-2 Polyclonal Antibody, 20ul PCR Series It's non-treatedAPLP2 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