Vimentin Monoclonal Antibody, 50ul[BT-MCA1285] Site-directed Mutagenesis 59 kDa and 66 kDa

59 kDa and 66 kDa

reducing cell damage

ABHD11 is deleted in Williams syndrome

In particular this protein represses the circadian clock transcription factor aryl hydrocarbon receptor nuclear translocator-like protein 1 (ARNTL)

This gene may also play a role in the stiff man syndrome

Vimentin Monoclonal Antibody, 50ul[BT-MCA1285] Site-directed Mutagenesis 59 kDa and 66 kDaThis gene encodes a member of the intermediate filament family. Intermediate filamentents, along with microtubules and actin microfilaments, make up the cytoskeleton. The protein encoded by this gene is responsible for maintaining cell shape, integrity of the cytoplasm, and stabilizing cytoskeletal interactions. It is also involved in the immune response, and controls the transport of low density lipoprotein (LDL) derived cholesterol from a lysosome