Anti-ABCA1 Antibody, clone AB.H10

Descrição detalhada : Mutations in the ABCA1 gene are associated with Tangier disease (TD). TD is an autosomal recessive disorder results from an absence of plasma HDL, cholesterol ester depositing in the reticulo-endothelial system and disorders in cellular lipid trafficking. It is expressed on the plasma membrane and the Golgi complex, and is regulated by cholesterol flux. Regulation of the cholesterol flux between HDL and macrophages is competitive between ABCA1 and SR-BI.
Sinónimos : ATP-binding cassette transporter 1, ABC-1, Cholesterol efflux regulatory protein
Armazenamento : -20°C
Embalagem : 1X1EA