APBA1 Polyclonal Antibody, 100ul Immunoassays Mutations in this gene have

Mutations in this gene have been found to cause fish-eye disease as well as LCAT deficiency

and is upregulated by nerve growth factor

Two splice variants have been identified for this gene

Its initiating methionine residue is post-translationally removed

Pseudogenes of this gene are found on chromosome 7

APBA1 Polyclonal Antibody, 100ul Immunoassays Mutations in this gene haveThe protein encoded by this gene is a member of the X11 protein family. It is a neuronal adapter protein that interacts with the Alzheimer's disease amyloid precursor protein (APP). It stabilizes APP and inhibits production of proteolytic APP fragments including the A beta peptide that is deposited in the brains of Alzheimer's disease patients. This gene product is believed to be involved in signal transduction processes. It is also regarded as a