SENP6 Polyclonal Antibody, 100ul Stepper PTM:O-glycosylated

PTM:O-glycosylated

Mutations in this gene are associated with autosomal SCID (severe combined immunodeficiency disease)

including group 1 metabotropic glutamate receptors

Defects in this gene are a cause of familial amyloidosis Finnish type (FAF)

CLDN5 (claudin 5) encodes a member of the claudin family

SENP6 Polyclonal Antibody, 100ul Stepper PTM:O-glycosylatedUbiquitin like molecules (UBLs), such as SUMO1 (UBL1; MIM 601912), are structurally related to ubiquitin (MIM 191339) and can be ligated to target proteins in a similar manner as ubiquitin. However, covalent attachment of UBLs does not result in degradation of the modified proteins. SUMO1 modification is implicated in the targeting of RANGAP1 (MIM 602362) to the nuclear pore complex, as well as in stabilization of I kappa B alpha (NFKBIA; MIM 164008)