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Ab213749

Manufactured by Abcam
Sourced in United States

Ab213749 is a laboratory equipment product manufactured by Abcam. It is designed to perform a specific function in a research or laboratory setting. The core function of this product is to facilitate a particular experimental or analytical process. However, a detailed and unbiased description of the product's features and capabilities is not available at this time.

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5 protocols using ab213749

1

Cytokine Profiling by ELISA

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Cell culture supernatants were analyzed for cytokines by standard ELISA after comparison to recombinant standard. IL-4 (Clone 11B11 and 554390 BD Biosciences, San Jose, CA), IL-5, IL-13 (DY405, DY413, R&D systems, Minneapolis, MN), IL-17 (BMS2017, Thermofisher scientific, Waltham MA), IFN-γ (555142, BD Biosciences, San Jose, CA), IL-1, IL-6, TNF (ab210895, ab213749 and ab212073, Abcam, Cambridge MA) were used as antibodies pairs and capture signals were amplified using Streptavidin-horseradish peroxidase conjugate (51–9002813, BD Biosciences, San Jose, CA). The plate was further developed using TMB substrate solution (N301, Thermofisher scientific, Waltham MA) and detected at the absorbance wavelength of 450 nm.
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2

Cytokine and Amyloid-β Quantification

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Following pentobarbital euthanasia, mice were perfused of blood as above. Brains were then harvested and deaggregated by pressing gently through 40 μm cell strainers in 3 ml of DMEM medium. The homogenate was then centrifuged (1400 × g, 5 min, 4 °C), and supernatants were collected. IL-1β, IL-6, TNF, and amyloid β protein levels were detected using standard ELISA after comparison to recombinant standard (cytokines: ab210895, ab213749, and ab212073, Abcam, Cambridge, MA; amyloid β64 (link): capture antibody: #800701, detection antibody: #805504 or #805404, 1:100, Biolegend, San Diego, CA).
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3

Quantifying Neuroinflammatory Markers

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Brain homogenates were collected and then supernatants were used to quantify IL-1β, IL-6, TNF, IFN-β and Aβ proteins using standard ELISA after comparison to recombinant standard (Cytokines: ab210895, ab213749 and ab212073, Abcam, Cambridge MA; DY8234–05, R&D systems, Minneapolis, MN. Aβ capture antibody: #800701, detection antibody: #805504 or #805404, 1:100, Biolegend, San Diego, CA)
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4

Quantification of Serum IL-6 Levels

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We measured the serum levels of IL-6 in the blood samples using commercial mouse kits (ab213749 and ab100697; Abcam, Cambridge, MA, USA) according to the manufacturer’s protocol. We added 50 μL of samples to each of the wells in 96-well antibody-coated plates and then incubated these for 2 h at room temperature. We then loaded 50 μL of the detector antibody solution into each well and incubated the plates for an additional 1 h at room temperature. Next, we added 50 μL of HRP–streptavidin solution (ab210901; Abcam) to each well and once again incubated the plates for 1 h at room temperature. Finally, we added 100 μL of tetramethylbenzidine substrate to each well and incubated the plates for another 10 min in the dark at room temperature. We stopped the reaction by adding 100 μL of stop solution. We read the absorbance at a wavelength of 450 nm and expressed the results in pg/mL.
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5

Quantification of Serum IL-6 and IL-10

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The blood samples were used to measure serum levels of IL-6 and IL-10 using mice commercial kits (ab213749 and ab100697; Abcam, Cambridge, MA, USA) following the manufacturer instructions. Samples of 50 μL were added to each well of the 96-well antibody-coated plates and then incubated for 2 h at room temperature. The detector antibody solution (50 μL) was loaded into each well and the plates were incubated for 1 h at room temperature. Next, 50 μL of the HRP-Streptavidin solution (ab210901, Abcam) was added, and the plates were incubated for another 1 h. Then, 100 μL of TMB substrate was added to each well and the plates were incubated for 10 min in the dark. The reaction was stopped with the addition of 100 μL stop solution. A wavelength 450 nm was used to read the absorbance and the results are expressed in pg/mL.
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