CD55 Polyclonal Antibody, 100ul[BT-AP01514] 3D Cell Culture Consumables Defects in PEX7 cause peroxisome

Defects in PEX7 cause peroxisome biogenesis disorders (PBDs)

KRT18 encodes the type I intermediate filament chain keratin 18

The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis

• Used for various mixing applications with optional adapters

CD55 Polyclonal Antibody, 100ul[BT-AP01514] 3D Cell Culture Consumables Defects in PEX7 cause peroxisomeCD53 molecule encoded by CD53 is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein that is known to complex with