FAM111B Polyclonal Antibody, 20ul Cell Dissociation and it has been proposed

and it has been proposed that mannose binding by this protein leads to internalization of antigen into Birbeck granules and providing access to a nonclassical antigen-processing pathway

which is also referred to as mental retardation X-linked with macrocephaly

transferring glycosyl groups and glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase activity

This protein was shown to interact with mitotic checkpoint proteins including Mad2

This protein lacks one amino acid of the conserved heme binding site

FAM111B Polyclonal Antibody, 20ul Cell Dissociation and it has been proposedFAM111B encodes a protein with a trypsin like cysteine serine peptidase domain in the C terminus. Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP). Affected individuals display mottled pigmentation, telangiectasia, epidermal atrophy, tendon contractures, and progressive pulmonary fibrosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A paralog