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The ApoE2 is a lab equipment product designed for the analysis and quantification of apolipoprotein E (ApoE) in biological samples. It serves as a tool for researchers and scientists working in the fields of lipid metabolism, cardiovascular disease, and neurodegenerative disorders.

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2 protocols using apoe2

1

Cytokine Secretion Assay Using Fibronectin and ApoE2

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Wells of a 96-well Maxisorp (Nunc) plate were co-coated with fibronectin (Millipore, catalog no. FC010) or ApoE2 (Peprotech, catalog no. 350-12) with human anti-KLH (each at 5 μg/mL in PBS) at room temperature for 2 hours, then washed twice with PBS and preincubated with RPMI1640 containing 10% FBS for 2 hours. THP-1 cells (2 × 105 cells/well) or tolerogenic human DCs (7 × 104 cells/well; generated as described in “Differentiation of primary human DCs and generation of knockout DCs”) were plated on the coated wells. In some experiments, cells were washed, resuspended in X-Vivo 15 media (Lonza, catalog no. 04-418Q), and incubated with the designated antibodies (5 μg/mL) in solution at room temperature for 20 minutes before plating onto coated wells. After overnight incubation at 37°C, culture supernatants were collected, and cytokine secretion was measured by Luminex assay using human IL8 simplex kits (Thermo Fisher Scientific, catalog no. EPX01A-10204-901, RRID: AB_2575769) or human TNFα simplex kits (Thermo Fisher Scientific, catalog no. EPX01A-10223-901, RRID: AB_2575781) according to the manufacturer's instructions.
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2

Apolipoprotein Interactions with Lipid Nanoparticles

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LNPs and Apos were incubated in ddH2O water overnight at 4 °C. LNPs equivalent of 5 µg encapsulated plasmid DNA were incubated with 3 µg of each of the different human Apos; ApoA1 (Sigma, SRP4693), ApoB (Sigma, 178456), ApoC3 (Sigma, A3106), ApoD (Sigma, SRP4326), ApoE2 (Peprotech, 350-12), ApoE4 (Peprotech, 350-04) and ApoH (Sigma, G9173), unless otherwise stated, in a final volume of 200 µl. For control experiments (i.e. LNP only), LNPs were incubated with ddH2O water (in the absence of any apolipoprotein) overnight at 4 °C in a final volume of 200 µl. For Cryo TEM reactions were set up as described above in the absence of ddH2O.
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