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蛋白别名为：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为：5828；蛋白质ID:P28328
应用类型
WB，IHC-p，ELISA补充：最优的抗体稀释比例需要基于客户实验进行优化.建议的起始稀释比例如下: 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
