INF2 Polyclonal Antibody - E-AB-18555 Cells in 3D-scaffolds Mutations in this gene are

Mutations in this gene are associated with dentinogenesis imperfecta and dentin dysplasia

AF3877-200

where it has been shown to interact with the retinoid X receptor alpha and possibly other nuclear elements

and therefore can not mediate the intracellular signal transduction through protein phosphorylation

and C-terminal regulatory domains which are susceptible to the most variance

INF2 Polyclonal Antibody - E-AB-18555 Cells in 3D-scaffolds Mutations in this gene areINF2 Polyclonal Antibody Sizes: 60L, 120L, 200L Catalogue Numbers: E AB 18555 60, E AB 18555 120, E AB 18555 200 Citations, Manuals and MSDS Available upon request. Abbreviation: INF2 Target Synonym: C14orf151; C14orf173; CMTDIE; DKFZp762A0214; FLJ22056; FSGS5; HBEAG binding protein 2 binding protein C; HBEBP2 binding protein C; HBEBP2 binding protein C; INF 2; inf2; INF2; Inverted formin 2; Inverted formin FH2 and WH2 domain containing; Inverted