APLP-2 Polyclonal Antibody, 20ul PCR Series When bound to KRT17

When bound to KRT17

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

ensuring maximum productivity and efficiency

Transparent and scale-free for easy observation

Yeast alpha-aminoadipate dehydrogenase converts alpha-biosynthetic-aminoadipate semialdehyde to alpha-aminoadipate

APLP-2 Polyclonal Antibody, 20ul PCR Series When bound to KRT17APLP2 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