AASS Polyclonal Antibody, 50ul DNA Fragments |disease:A chromosomal aberration involving NFKB2

|disease:A chromosomal aberration involving NFKB2 is found in a cutaneous T-cell leukemia (C-TCL) cell line

and paroxysmal extreme pain disorder

the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs

The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis

AASS Polyclonal Antibody, 50ul DNA Fragments |disease:A chromosomal aberration involving NFKB2AASS encodes a bifunctional enzyme (aminoadipate semialdehyde synthase) that catalyzes the first two steps in the mammalian lysine degradation pathway. The N terminal and the C terminal portions of this enzyme contain lysine ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha aminoadipic semialdehyde. Mutations in AASS are associated with familial hyperlysinemia.