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Nbp1 69750

Manufactured by Novus Biologicals

NBP1-69750 is a laboratory product manufactured by Novus Biologicals. It is a tool used for research purposes, but a detailed description is not available while maintaining an unbiased and factual approach.

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2 protocols using nbp1 69750

1

Immunohistochemistry of Brain Sections

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Immunohistochemical analysis of 40-μm brain sections were conducted essentially as described previously (Niu et al., 2013 (link), Niu et al., 2015 (link)). The following primary antibodies were used: BrdU (rat BU1/75, 1:500, Accurate Chemical), NeuN (MAB377, mouse, 1:500, Millipore), SOX2 (AB5603, rabbit, 1:500, Millipore), DCX (SC-8066, goat, 1:150, Santa Cruz Biotechnology), TH (chick, 1:1,000, Aves), DARPP32 (no. 2302, rabbit, 1:500, Cell Signaling Technology), CTIP2 (AB18465, rat, 1:500, Abcam), DAT (MAB369, rat, 1:200, Millipore), DDC (Ab3905, rabbit, 1:500, Abcam), VMAT2 (NBP1-69750, rabbit, 1:250, Novus), VGLUT1 (135311, mouse, 1:1,000, Synaptic), CHAT (AB144P, goat, 1:200, Chemicon), and GABA (A2052, rabbit, 1:500, Sigma). Alexa Fluor 488-, 594-, or 647-conjugated corresponding secondary antibodies from Jackson ImmunoResearch were used for indirect fluorescence. Images were taken using a Zeiss LSM510 confocal microscope. A Cell Counter software plugin in the ImageJ program was used to count cells. Data were obtained from one-sixth of the sections spanning the whole striatal region in each mouse. A representative image was shown from at least four similar ones. Confocal images were Z series projections unless otherwise indicated in the figure legends.
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2

Immunohistochemical Labeling of Neurological Markers

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Paraffin-embedded human brain sections or free-floating mouse brain sections sliced by cryotome were treated with 0.3% H2O2 for 10 min. Sections were washed three times in PBS and blocked in 1% BSA, 0.3% Triton X-100, for 1 h, followed by overnight incubation with a tyrosine hydroxylase (TH) antibody (Abcam, AB112; 1: 1000), anti-T22, anti-Tau N368, anti-ApoE, anti-AEP, anti-VMAT2 (Novus, NBP1-69750), or AT-8 antibody (1: 500) at 4°C. Then, the sections were incubated with the matched fluoro-conjugated secondary antibody for 2 h at room temperature, followed by three washes in PBS. The slides were washed three times in PBS and covered with a glass using mounting solution, after DAPI staining for 5 min. Human brain sections were treated with 10 mM cupric sulfate in ammonium acetate buffer (50 mM) for 15 min to eliminate lipofuscin-like auto fluorescence.
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