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Human il 17 elisa kit

Manufactured by R&D Systems
Sourced in United States

The Human IL-17 ELISA kit is a quantitative sandwich enzyme-linked immunosorbent assay (ELISA) for the measurement of human interleukin-17 (IL-17) levels in cell culture supernatants, serum, and plasma.

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3 protocols using human il 17 elisa kit

1

Quantifying IL-17 Levels in Psoriasis Plaque Scales

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All patients were treated initially with a topical application of 5% salicylic acid ointment for desquamation. Plaque scales were collected from the most representative lesions. The same amount of scale from each patient was weighed. Then, plaque scales were suspended in phosphate-buffered saline (PBS) without calcium and magnesium and disrupted with Sonics Vibracell VCX130 in impulsing mode. Cell suspension was centrifuged for 10 minutes at 5000 x g. Then, scale samples were subdivided into small aliquots to be stored at -80°C until tested for cytokine levels. The concentration of IL-17 in the patient plaque scales was determined with the use of Human IL-17A High Sensitivity ELISA kit (eBioscience, Vienna, Austria) and Human IL-17 ELISA kit (R&D Systems, Minneapolis, MN, USA), according to the manufacturers' instructions. With Human IL-17A High Sensitivity ELISA kit, we have reached very high results, which were out of range. That is why we repeated the analysis with Human IL-17 ELISA kit (R&D Systems, Minneapolis, MN, USA).
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2

Quantification of Plasma IL-17 and IL-23

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Enzyme-linked immunosorbent assay (ELISA) was performed using Human IL-17 ELISA Kit (R&D Systems, Inc., Minneapolis, MN, USA) and Human IL-23 ELISA Kit (R&D Systems, Inc., Minneapolis, MN, USA) to measure the plasma IL-17 and IL-23 levels according to the manufacturer's instructions.
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3

Quantitative Serum IL-17 ELISA Assay

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Serum IL-17 levels were measured by quantitative sandwich ELISA using the Human IL-17 ELISA Kit (R & D Systems, Minneapolis, MN, USA). The wells had been pre-coated with anti-IL-17 monoclonal antibody (mAb). First, the Assay Diluent RD1-36 was added (100 µl/well). Then, 100 µl/well of serum samples, control or standard was added followed by incubation for 4 hours at room temperature. After washing, 200 µl of IL-17 conjugate was added to each well and incubated for 1 hour at room temperature. After washing and aspiration, the substrate solution was added to the wells and incubated for 30 minutes at room temperature. After that, the stop solution was added and the absorbance values were determined at 450 nm. The results were expressed as pg/ml.
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