CD59 Polyclonal Antibody, 100ul[BT-AP01987] General Lab Use Lewis x (CD15)

Lewis x (CD15)

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This gene encodes a PHOX domain- and RGS domain-containing protein that belongs to the sorting nexin (SNX) family and the regulator of G protein signaling (RGS) family

is reported to be essential for meiotic homologous recombination and may thus play an important role in generating diversity of genetic information

CD59 Polyclonal Antibody, 100ul[BT-AP01987] General Lab Use Lewis x (CD15)CLN5 is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.