IL-13R alpha 1(Phospho Tyr405) Polyclonal Antibody, 20ul Buffer Solutions The gene is deleted in

The gene is deleted in Williams-Beuren syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11

respectively

Multiple alternatively spliced transcript variants encoding different isoforms have been observed for MOK

TAFs contribute to promoter recognition and selectivity and act as antiapoptotic factors

like most family members

IL-13R alpha 1(Phospho Tyr405) Polyclonal Antibody, 20ul Buffer Solutions The gene is deleted inThe protein encoded by this gene is a subunit of the interleukin 13 receptor. This subunit forms a receptor complex with IL4 receptor alpha, a subunit shared by IL13 and IL4 receptors. This subunit serves as a primary IL13 binding subunit of the IL13 receptor, and may also be a component of IL4 receptors. This protein has been shown to bind tyrosine kinase TYK2, and thus may mediate the signaling processes that lead to the activation of JAK1, STAT3