Hck(Phospho Tyr521) Polyclonal Antibody, 20ul Glassware Sets Mutations in this gene are

Mutations in this gene are associated with gastrointestinal stromal tumors| mast cell disease| acute myelogenous lukemia| and piebaldism

and subsequently forms a complex with IL18 receptor beta subunit

Contains 1 EF-hand domain

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Hck(Phospho Tyr521) Polyclonal Antibody, 20ul Glassware Sets Mutations in this gene areThe protein encoded by this gene is a member of the Src family of tyrosine kinases. This protein is primarily hemopoietic, particularly in cells of the myeloid and B lymphoid lineages. It may help couple the Fc receptor to the activation of the respiratory burst. In addition, it may play a role in neutrophil migration and in the degranulation of neutrophils. Multiple isoforms with different subcellular distributions are produced due to both