Mutations in the PKHD1 gene, which encodes fibrocystin, cause autosomal recessive polycystic kidney disease (ARPKD). Unfortunately, the lack of specific antibodies to the mouse protein impairs the study of splicing, post-translational processing, shedding, and temporal and spatial expression of endogenous fibrocystin at the cellular and subcellular level.
应用类型
IHC,ICC,FCM
免疫原
Purified recombinant fragment of mouse PKHD1 (AA: 3878-4060) expressed in E. Coli.
