The protein encoded by this gene plays a crucial role in B-cell development. Mutations in this gene cause X-linked agammaglobulinemia type 1, which is an immunodeficiency characterized by the failure to produce mature B lymphocytes,and associated with a failure of Ig heavy chain rearrangement.
应用类型
该抗BTK产品的应用类型详情查看产品说明书。
免疫原
Full length human recombinant protein of human BTK (NP_000052) produced in HEK293T cell.
