Immunofluorescence
Three cryosections on each slide were stained with a single antibody. The fourth slice was used as a negative control (primary antibody omitted). The tissue was fixed with cold acetone for 10 minutes, rinsed in phosphate buffered saline (PBS) and incubated with the primary antibody diluted in 1% bovine serum albumin (BSA) in PBS for 1 hour at room temperature.Rabbit anti human antibodies and dilutions used:e) ZNF133 (38332), most suitable concentration 1:100
Western blot
0.2-1 ug/ml
ELISA Titer: 1:312500
Positive Control: THP-1 cell lysate