peroxisomal biogenesis factor 16(PEX16) Homo sapiens The protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described. [provided by RefSeq, Jul 2008],

推荐稀释比 WB:1/500-1/1000;ELISA:1/10000

Western blot analysis of of PEX16 in PC-12 lysates using PEX16 antibody.

-25 ~ -15℃保存，收到货之后有效期1年，避免反复冻融。