PEX2 encodes an integral peroxisomal membrane protein required for peroxisome biogenesis. Peroxisomal biogenesis factor 2 is thought to be involved in peroxisomal matrix protein import. Mutations in PEX2 result in one form of Zellweger syndrome and infantile Refsum disease. Alternative splicing results in multiple transcript variants encoding the same protein蛋白別名為：PEX2; PAF1; PMP3; PMP35; PXMP3; RNF72; Peroxisome biogenesis factor 2; 35 kDa peroxisomal membrane protein; Peroxin-2; Peroxisomal membrane protein 3; Peroxisome assembly factor 1; PAF-1; RING finger protein 72;基因ID為：5828；蛋白質ID:P28328
應用類型
WB，IHC-p，ELISA補充：最優的抗體稀釋比例需要基于客戶實驗進行優化.建議的起始稀釋比例如下: WB: 1:500-1:2000, IHC-p: 1:100-1:300, ELISA: 1:20000. Not yet tested in other applications.
免疫原
合成多肽：the N-terminal region of human Peroxin 2. at AA rangle: 1-80
