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. Author manuscript; available in PMC: 2018 Mar 1.
Published in final edited form as: Neurobiol Aging. 2016 Dec 1;51:54–66. doi: 10.1016/j.neurobiolaging.2016.11.015

Table 2.

Effects of DAT knock-down on striatal DAT and TH-immunoreactivity

striatal DAT-immunoreactivity
rostral medial caudal
Age WT DAT-KD WT DAT-KD WT DAT-KD
Pups (3–4 days) 1.00 ± 0.10 0.54 ± 0.05** 1.00 ± 0.10 0.57 ± 0.05** 1.00 ± 0.09 0.66 ± 0.07*
aged (18 months) 1.00 ± 0.09 0.42 ± 0.02** 1.00 ± 0.06 0.42 ± 0.04** 1.00 ± 0.11 0.41 ± 0.04**
striatal TH-immunoreactivity
rostral medial caudal
Age WT DAT-KD WT DAT-KD WT DAT-KD
Pups (3–4 days) 1.00 ± 0.05 1.03 ± 0.05 1.00 ± 0.05 1.10 ± 0.07 1.00 ± 0.04 1.16 ± 0.07
aged (18 months) 1.00 ± 0.11 0.94 ± 0.09 1.00 ± 0.11 0.98 ± 0.13 1.00 ± 0.13 0.88 ± 0.12

Striatal DAT and TH immunoreactivity. A coronal section of the rostral, medial and caudal striatum was used for each mouse (pups, WT n=7, DAT-KD =6; 18 months, WT=7, DAT-KD n=7). Data are represented as ratios to respective mean of WT (mean ± SEM) for comparison purposes only; all statistical analyses were performed on raw numbers (2×3 genotype x striatal subregion ANOVA for each age group, Holm-Sidak *p<0.05, **p<0.01 compared to respective WT). Tissue processing and immunohistochemistry for pups and aged mice were performed separately; therefore fluorescence intensities were not compared between ages. Intensity values were not saturated providing similar signal to noise ratio for all age groups.

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