FXL18 Rabbit Polyclonal Antibody, 100ul Organelle Studies similarity:Contains 3 C2H2-type zinc fingers

similarity:Contains 3 C2H2-type zinc fingers

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

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

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

and multi-channel adjustable models

FXL18 Rabbit Polyclonal Antibody, 100ul Organelle Studies similarity:Contains 3 C2H2-type zinc fingersThe 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