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

Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex| leading to epilepsy| mental retardation| subcortical band heterotopia ("double cortex" syndrome) in females and lissencephaly ("smooth brain&quo

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

The protein encoded by AXL (AXL receptor tyrosine kinase) is a member of the Tyro3-Axl-Mer (TAM) receptor tyrosine kinase subfamily

Guanine nucleotide exchange factor (GEF)

Contains 12 LRR (leucine-rich) repeats

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