Sum1, belongs to the WD repeat SMU1 family. Human SMU1 is a component of the spliceosome fSAP57. It is possible that the mutation in Smu1 affects spliceosome function, resulting in generation of improper splice variants, which could explain the phenotypes of tsTM18 cells. Some results suggest that Smu1 participates in at least two steps of splicing: splice-site choice and control of accuracy. This antibody is a rabbit polyclonal antibody raised against a region of human REDD1 antigen.
Western Blot: Mouse Liver Tissue, 1:200-1:2000; IHC: Human Kidney Tissue, 1:20-1:200; IF: HepG2 Cells, 1:10-1:100
Type: Primary
Antigen: SMU1
Clonality: Polyclonal
Clone:
Conjugation: Unconjugated
Epitope:
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat