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NYX Rabbit Polyclonal Antibody, 20ul Molecular Sciences The protein encoded by this

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NYX Rabbit Polyclonal Antibody, 20ul Molecular Sciences The protein encoded by thisThe 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

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Description

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

these dishes are a reliable tool for all of your cell culture needs

Pimase (DNA) subunit 1 ncoded by PRIM1 is the small

trans-Golgi resident protein involved in glycoconjugate biosynthesis

while other individuals have an allele encoding a protein that is predicted to be non-functional

NYX Rabbit Polyclonal Antibody, 20ul Molecular Sciences The protein encoded by thisThe 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

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