该B9D1 Polyclonal Antibody. This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17.
应用类型
IHC
免疫原
Recombinant fusion protein of human B9D1 (NP_056496.1).
