PEX6 Polyclonal Antibody, 50ul Liquid Storage Consumables Also component of a CK2-SPT16-SSRP1

Also component of a CK2-SPT16-SSRP1 complex composed of SSRP1

Mutations in KCNT1 cause the early-onset epileptic disorders

The protein is required for complex I assembly and electron transfer activity

globular and stalk domains

A nucleolar staining may be due to nuclear targeting of an isoform lacking the transmembrane domain (By similarity)

PEX6 Polyclonal Antibody, 50ul Liquid Storage Consumables Also component of a CK2-SPT16-SSRP1This gene encodes a member of the AAA (ATPases associated with diverse cellular activities) family of ATPases. This member is a predominantly cytoplasmic protein, which plays a direct role in peroxisomal protein import and is required for PTS1 (peroxisomal targeting signal 1, a C terminal tripeptide of the sequence ser lys leu) receptor activity. Mutations in this gene cause peroxisome biogenesis disorders of complementation group 4 and