Application
WB to detect cellular Hice1 and Hice1-GFP expressed in human osteosarcoma U2OS cells (left image), and Hice1 upon siRNA treatment (right image), using at 1:1000 dilution. Nuclear matrix protein p84 is a loading control, blotted with p84 antibody (clone 5E10) at 1:5000 dilution. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
IP-WB assay to show that Hice1 co-immunoprecipitated with other Augmin components HAUS6 , HAUS2 and HAUS1 in U2OS cells.
Application
Immunohistochemical analysis of paraffin-embedded Human lymph tissue, using HICE1 antibody at 1:50 dilution.
Application
Immunofluorescence analysis of human osteosarcoma cell line U2OS, using HICE1 antibody at 1:50-1:200 dilution.
Application
Sample A: His-Hice1 (2x) B: His-Hice1 (1x) 7.5% SDS PAGE diluted at 1:500 The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.