Rabbit Polyclonal antibody to BTK (phospho Tyr223)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. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013]
Immunogen
KLH-conjugated synthetic peptide encompassing a sequence within the center region of human BTK (pY223). The exact sequence is proprietary.