Formalin-fixed and paraffin-embedded human tonsil tissue reacted with BPI Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
Western blot of BPI Antibody in HL-60 cell line lysates (35 ug/lane). BPI (arrow) was detected using the purified antibody.
BPI Antibody flow cytometry of HL-60 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.