BNI3L Polyclonal Antibody, 100ul Apoptosis & Autophagy Deficiency of this enzyme results

Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome)

HOXA5 is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression

granzyme M

EEF1A1 encodes an isoform of the alpha subunit of the elongation factor-1 complex

It is the prevalent mixed-lineage leukemia fusion gene associated with spontaneous acute lymphoblastic leukemia

BNI3L Polyclonal Antibody, 100ul Apoptosis & Autophagy Deficiency of this enzyme resultsThis gene encodes a protein that belongs to the pro apoptotic subfamily within the Bcl 2 family of proteins. The encoded protein binds to Bcl 2 and possesses the BH3 domain. The protein directly targets mitochondria and causes apoptotic changes, including loss of membrane potential and the release of cytochrome c.