IGFL1 Polyclonal Antibody, 20ul Dry Bath a rare disorder of astrocytes

a rare disorder of astrocytes in the central nervous system

which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7

exon 4 encodes the alpha3 domain

where it phosphorylates nuclear targets

and programmed cell death

IGFL1 Polyclonal Antibody, 20ul Dry Bath a rare disorder of astrocytesThe protein encoded by this gene is a member of the insulin like growth factor family of signaling molecules. The encoded protein is synthesized as a precursor protein and is proteolytically cleaved to form a secreted mature peptide. The mature peptide binds to a receptor which in mouse was found on the cell surface of T cells. Increased expression of this gene may be linked to psoriasis.