WB
Western blot analysis of MISP expression in HepG2 (A) whole cell lysates.
IHC
Immunohistochemical analysis of MISP staining in human
cervix carcinoma formalin fixed paraffin embedded tissue
section. The section was pre-treated using heat mediated
antigen retrieval with sodium citrate buffer (pH 6.0). The
section was then incubated with the antibody at room
temperature and detected using an HRP conjugated compact
polymer system. DAB was used as the chromogen. The section
was then counterstained with haematoxylin and mounted with
DPX.
FC
Flow cytometric analysis of HepG2 cells using Anti-MISP
Antibody. The cells were fixed with 2% paraformaldehyde (10
min) and then permeabilized with 90% methanol for 10 min.
The cells were incubated in 2% bovine serum albumin to block
non-specific protein-protein interactions followed by the
antibody at 37 °C for 60 min. The secondary antibody Goat
Anti-Rabbit IgG (H&L) - AF488 was incubated at 37 °C for 40
min. Isotype control antibody (blue line) was used under the
same condition.