CD55 Polyclonal Antibody, 20ul[BT-AP02468] Antibody Development They may thus play an

They may thus play an important role during growth and development

Mutations in CEP41 have been associated with Joubert Syndrome 15

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

Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule

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CD55 Polyclonal Antibody, 20ul[BT-AP02468] Antibody Development They may thus play anKRT18 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.