EphA10 Polyclonal Antibody, 50ul Mechanical Pipette Defects in this gene are

Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN)

The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins

tissue specificity:Highly expressed in placenta and lung

Expression of TPD52L2 may be a marker for breast cancer and acute lymphoblastic leukemia

When induced GABARAPL2 is first digested by ATG4 family enzymes to become its mature form: gABARAPL2-I

EphA10 Polyclonal Antibody, 50ul Mechanical Pipette Defects in this gene areEphrin receptors, the largest subfamily of receptor tyrosine kinases (RTKs), and their ephrin ligands are important mediators of cell cell communication regulating cell attachment, shape, and mobility in neuronal and epithelial cells (Aasheim et al. 2005 [PubMed 15777695]). See MIM 179610 for additional background on Eph receptors and ephrins.