Vimentin Polyclonal Antibody, 50ul[BT-AP09527] Cell Dissociation Mutations in this gene cause

Mutations in this gene cause nemaline myopathy type 5

The nascent protein contains a N-terminal signal peptide sequence

while gamma tubulin plays a critical role in the nucleation of microtubule assembly

Mutations in this gene and the genes encoding other EIF2B subunits have been associated with leukoencephalopathy with vanishing white matter

Keratin 15 encoded by KRT15 is a member of the keratin gene family

Vimentin Polyclonal Antibody, 50ul[BT-AP09527] Cell Dissociation Mutations in this gene causeVIM encodes a member of the intermediate filament family. Intermediate filamentents, along with microtubules and actin microfilaments, make up the cytoskeleton. Vimentin encoded by VIM 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 to the site of