EphA1 Polyclonal Antibody, 50ul[BT-AP02992] Plasma Mutations in this gene cause

Mutations in this gene cause hyperlipoproteinemia type IB

PIAS2 encodes a member of the protein inhibitor of activated STAT (PIAS) family

The protein activates STK11 leading to the phosphorylation of both proteins and excluding STK11 from the nucleus

An important paralog of this gene is GCNT2

which heterodimerizes with type I keratins to form hair and nails

EphA1 Polyclonal Antibody, 50ul[BT-AP02992] Plasma Mutations in this gene causeEPHA1 belongs to the ephrin receptor subfamily of the protein tyrosine kinase family. EPH and EPH related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their