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Murine il 1α and il 1β elisa kits

Manufactured by R&D Systems

The Murine IL-1α and IL-1β ELISA kits are designed for the quantitative determination of mouse interleukin-1 alpha (IL-1α) and interleukin-1 beta (IL-1β) in cell culture supernatants, cell lysates, tissue homogenates, and serum samples.

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2 protocols using murine il 1α and il 1β elisa kits

1

Quantification of IL-1α and IL-1β by ELISA and Bioassay

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ELISA was used for quantification of cytokines in cell-free supernatant and lavage fluid. Cells were centrifuged at 300× g for 5 minutes and the supernatant was collected and stored at −80°C. Murine IL-1α and IL-1β ELISA kits were purchased from R&D Systems. A Biotek Cytation-5 plate reader was used to quantify concentrations.
HEK-blue IL-1R1 cell-line used to measure IL-1α and IL-1β bioactivity was purchased from InvivoGen. For each experiment, 2.8×105 HEK IL-1R1 reporter cells/mL in DMEM (GIBCO) complete media were seeded in 180 μL per well. Twenty μL of each sample was added in duplicates without neutralizing antibodies, with anti-IL-1α neutralizing antibodies (Fisher Scientific), anti-IL-1β neutralizing antibodies (R&D Systems), or both and incubated overnight at 37°C with 5% CO2. The supernatant was collected and incubated with QUANTI-Blue (InvivoGen) for 30 minutes. SEAP detection and concentration calculations were measured on the Biotek Cytation-5 instrument. IL-1α and IL-1β concentrations were calculated based on a set of standards of known bioactive IL-1α and IL-1β concentrations and presented as pg/mL.
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2

Quantification of IL-1α and IL-1β by ELISA and Bioassay

Check if the same lab product or an alternative is used in the 5 most similar protocols
ELISA was used for quantification of cytokines in cell-free supernatant and lavage fluid. Cells were centrifuged at 300× g for 5 minutes and the supernatant was collected and stored at −80°C. Murine IL-1α and IL-1β ELISA kits were purchased from R&D Systems. A Biotek Cytation-5 plate reader was used to quantify concentrations.
HEK-blue IL-1R1 cell-line used to measure IL-1α and IL-1β bioactivity was purchased from InvivoGen. For each experiment, 2.8×105 HEK IL-1R1 reporter cells/mL in DMEM (GIBCO) complete media were seeded in 180 μL per well. Twenty μL of each sample was added in duplicates without neutralizing antibodies, with anti-IL-1α neutralizing antibodies (Fisher Scientific), anti-IL-1β neutralizing antibodies (R&D Systems), or both and incubated overnight at 37°C with 5% CO2. The supernatant was collected and incubated with QUANTI-Blue (InvivoGen) for 30 minutes. SEAP detection and concentration calculations were measured on the Biotek Cytation-5 instrument. IL-1α and IL-1β concentrations were calculated based on a set of standards of known bioactive IL-1α and IL-1β concentrations and presented as pg/mL.
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