Prostates from transgenic mice were dissected using a dissection microscope, fixed in 10% buffered formalin and embedded in paraffin.
Spleens of asymptomatic mice were dissected 3 weeks after transplant in B6/SJL mice (CD45.1+), and cells were treated with ACK buffer as described above.
Limb muscles from P10-P14 wild-type mice were dissected and subjected to a gentle collagenase (Sigma) and dispase (Gibco) digestion.
After the scans, the mice were dissected, and the abdomen was systematically and meticulously examined for tumors.
The euthanized mice were dissected, the organs were weighed, and the radiation in each organ was measured using a PerkinElmer gamma counter.
Alternatively, selected organs from mice were dissected and placed inside the imaging system.
Hippcampi of mice were dissected out, put in microtube and frozen immediately in liquid nitrogen.
The mice were dissected and tissues were immediately fixed in buffered formalin.
The mice were dissected and analyzed 10 days after the final injection.
After eight weeks, the mice were dissected and spleen cells analyzed by FACS.
At autopsy, mice were dissected, photographed, and examined for the presence of liver tumors.
