p53(Phospho Ser15) Polyclonal Antibody, 50ul Filtration Mutations in ACVRL1 are associated

Mutations in ACVRL1 are associated with hemorrhagic telangiectasia type 2

lens and nerve

a combination of nephronophthisis and retinitis pigmentosa

The members of this family function in the Notch signaling pathway that regulates determination of cell fate during development

SOD2 is a member of the iron/manganese superoxide dismutase family

p53(Phospho Ser15) Polyclonal Antibody, 50ul Filtration Mutations in ACVRL1 are associatedThis gene encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in this gene are associated with a variety of human cancers, including hereditary cancers such as Li Fraumeni syndrome.