CD55 Polyclonal Antibody, 20ul[BT-AP02468] Antibody Development an autosomal recessive disease in

an autosomal recessive disease in which few or no gamma globulins or antibodies are made

limb girdle muscular dystrophy

facilitating identification and marking

Mutations in CEP41 have been associated with Joubert Syndrome 15

Differential expression of this gene may be associated with progression of breast and prostate cancer

CD55 Polyclonal Antibody, 20ul[BT-AP02468] Antibody Development an autosomal recessive disease inKRT18 encodes the type I intermediate filament chain keratin 18. Keratin 18, together with its filament partner keratin 8, are perhaps the most commonly found members of the intermediate filament gene family. They are expressed in single layer epithelial tissues of the body. Mutations in this gene have been linked to cryptogenic cirrhosis. Two transcript variants encoding the same protein have been found for KRT18.