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Recommended positive controls: Jurkat, Raji, NCI-H929, NT2D1.
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
CLN3 is a highly glycosylated, hydrophobic, 438-amino acid protein with 6 transmembrane domains. The CLN3 protein localizes to the lysosomal membrane and plays a role in lysosomal function. It may act as a chaperone involved in the folding and unfolding of other proteins, namely subunit C of the ATP synthase complex. Mutations in the CLN3 gene cause Batten disease, a recessively inherited neurodegenerative disorder of childhood caused by lysosomal accumulation of hydrophobic material, mainly ATP synthase subunit C. Batten disease is the most common form of a group of disorders known as neuronal ceroid lipofuscinoses (NCLs). Symptoms of Batten disease include progressive loss of vision, seizures, and psychomotor disturbances.
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Protein Aliases: Batten disease protein; Battenin; ceroid-lipofuscinosis, neuronal 3; CLN 3; MGC102840; Protein CLN3
Gene Aliases: BTS; CLN3; JNCL
UniProt ID: (Human) Q9UP14
Entrez Gene ID: (Human) 1201
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