NYX Rabbit Polyclonal Antibody, 20ul Molecular Sciences Overexpression of this gene may

Overexpression of this gene may be associated with the majority of solid tumor types

which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin

coli as well as the virulence factors of such bacteria as Shigella

The protein encoded by this gene is a major sialoglycoprotein found on the surface of thymocytes| T lymphocytes| monocytes| granulocytes| and some B lymphocytes

Two transcript variants encoding the same protein have been identified for PARK7

NYX Rabbit Polyclonal Antibody, 20ul Molecular Sciences Overexpression of this gene mayThe product of this gene belongs to the small leucine rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1) also called X linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision myopia hyperopia nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations