The ability of the Technicon H1 haematology analyser to quantify rat
lymphocyte subsets using an immunoperoxidase staining technique was as
sessed. The instrument was standardised and use for human lymphocyte s
ubset analysis employing the standard reagent kit supplied by Technico
n (now Bayer Diagnostics). Rat samples were then analysed using the sa
me reagents, substituting the appropriate monoclonal antibodies agains
t rat Pan B, Pan T, T4 and T8 lymphocytes. Poor separation of the lymp
hocytes was encountered. Further substitutions of the standard reagent
s were made, which included the use of rabbit antimouse IgG: biotin co
njugate and streptavidin horseradish peroxidase (both non-cross-reacti
ve with rat). No separation of lymphocyte subsets was achievable, desp
ite additional steps to alter the software gain factors to accommodate
analysis of rat blood.