FXL18 Rabbit Polyclonal Antibody, 100ul Organelle Studies and multi-channel adjustable models

and multi-channel adjustable models

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

cholesterol

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

The reversible posttranslational modification of proteins by the addition of small ubiquitin-like SUMO proteins (see SUMO1

FXL18 Rabbit Polyclonal Antibody, 100ul Organelle Studies and multi-channel adjustable modelsThe 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