GFAP Monoclonal Antibody(5C8), 50ul Cell Senescence Mutations in this gene may

Mutations in this gene may be associated with osteoarthritis in human patients

This protein forms a complex with several other members of the RAD51 family

This gene is located 7 kb telomeric to gene family member ABCB2

Read-through transcription also exists between this gene and the downstream melanoma antigen family A

Another cullin

GFAP Monoclonal Antibody(5C8), 50ul Cell Senescence Mutations in this gene mayThis gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms.