Fig. 5From: Assembly of transgenic human P301S Tau is necessary for neurodegeneration in murine spinal cordRelevance of murine Tau for assembly and neurodegeneration. The values of AT100 immunoreactivity (a) and motor neuron numbers (b) of homozygous 7–8-month-old mice transgenic for full-length human P301S Tau on a normal murine Tau background are taken as 100%. The results are expressed as means ± S.E.M. (5 animals/group). Two-tail unpaired student t-test revealed no significant difference (p = 0.78 and p = 0.85 respectively). c Survival of mice transgenic for full-length human P301S Tau compared to those on a murine Tau null background (20 animals/group). Two-tail unpaired student t-test revealed no significant difference (p = 0.09). n.s., not significant. d Immunoblots of sarkosyl-insoluble Tau from spinal cord of 7–8-month-old mice transgenic for full-length human P301S Tau, in presence (lane 1) or absence (lane 2) of murine Tau. Lane 3 shows lack of immunoreactivity in an age-matched wild-type mouse. Antibody AT100 is specific for Tau phosphorylated at T212/S214/T217 and identifies filamentous Tau. T49 recognises murine Tau, whereas HT7 is specific for human TauBack to article page