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The A20216 is a laboratory centrifuge designed for general-purpose applications. It is capable of separating materials by centrifugal force. The centrifuge can accommodate a variety of sample sizes and tube types, and it is equipped with safety features to ensure proper operation.

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2 protocols using a20216

1

SUMO1 Localization in Mouse Brains

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Half brains of 22 week old male and female Non-Tg and SUMO1-Tg mice were dissected into 10% buffered formalin and kept at 4 oC overnight. Samples were then embedded in paraffin and sagittal sections were probed with primary antibodies corresponding to rabbit anti-SUMO1 (1:1000), mouse anti-SUMO1 (1:100; MAB 5718 Cell Signaling Technology), mouse anti-Synaptophysin (1:200; 61880 BD Biosciences), rabbit anti-NeuN (1:200; ABN78 Millipore), and mouse anti-GFAP (1:100; MAB 3670 Cell Signaling Technology). Alexafluor 488-conjugated anti-rabbit (1:1000; A20216 Invitrogen) and Cy3-conjugated anti-mouse (1:1000; 115–165-146 Jackson ImmunoResearch) were used as secondary antibodies.
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2

Immunohistochemical Analysis of S6-RP and ID3

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Standard immunohistology was performed on free-floating sections. Therefore, PFA fixed brains were infiltrated with 30% sucrose in PBS for 48 hours, cut into 40 mm sections, and stored in cryoprotectant (25% Glycerol, 25% Ethylene Glycol, 50% Phosphate Buffer pH 7.8) at À20 C until further use. Tissue sections were incubated with primary antibodies at the following dilutions: rabbit anti-S6-RP (1:50; Cell Signaling #2217S) or rabbit anti-ID3 (1:100; Abcam #Ab41834). Bound primary antibody was visualized using donkey anti-Rabbit antisera conjugated with Alexa 488 (1:500; Invitrogen #A-20216) for S6-RP or the tyramide signal amplification kit (PerkinElmer #NEL701A001KT) for ID3. Pictures were taken on a confocal SPE microscope. We counted individual ID3 positive cells and quantified the mean gray value for S6-RP in the SVZ using the software ImageJ.
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