FXL18 Rabbit Polyclonal Antibody, 100ul Organelle Studies Diseases associated with MARK1 include

Diseases associated with MARK1 include tauopathy and alzheimer disease

and multi-channel adjustable models

Mutations in this gene cause hereditary sensory and autonomic neuropathy with spastic paraplegia (HSNSP)

and thereby plays an important role in axon growth and axon guidance (By similarity)

COX5A (cytochrome c oxidase subunit 5A) encodes the nuclear-encoded subunit Va of the human mitochondrial respiratory chain enzyme

FXL18 Rabbit Polyclonal Antibody, 100ul Organelle Studies Diseases associated with MARK1 includeThe protein encoded by this gene is a member of a family of proteins that contain an approximately 40 amino acid F box motif. This motif is important for interaction with SKP1 and for targeting some proteins for degradation. The encoded protein has been shown to control the cellular level of FBXL7 a protein that induces mitotic arrest by targeting it for polyubiquitylation and proteasomal degradation. Members of the F box protein family such as FBXL18