UBE2S Polyclonal Antibody, 20ul High Speed Micro-Centrifuges Mutations in this gene are

Mutations in this gene are a cause of spastic ataxia 2

found on many cell types

Mutations have been associated with some forms of Zellweger syndrome| a heterogeneous group of peroxisome assembly disorders

miscellaneous:Its gene is located in the 5q region of the genome which is deleted in del(5q) interstitial deletion

this adapter allows for efficient and secure mixing of 8 Ø20mm test tubes (10-15mL)

UBE2S Polyclonal Antibody, 20ul High Speed Micro-Centrifuges Mutations in this gene areThis gene encodes a member of the ubiquitin conjugating enzyme family. The encoded protein is able to form a thiol ester linkage with ubiquitin in a ubiquitin activating enzyme dependent manner, a characteristic property of ubiquitin carrier proteins.