APLP-2 Polyclonal Antibody, 20ul PCR Series No more worries about retention

No more worries about retention or contamination

Transparent and scale-free for easy observation

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

When bound to KRT17

APLP-2 Polyclonal Antibody, 20ul PCR Series No more worries about retentionAPLP2 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