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Phadia immunocap system ecp feia

Manufactured by Thermo Fisher Scientific
Sourced in Sweden

The Phadia ImmunoCAP system ECP FEIA is a laboratory instrument used for the measurement of eosinophil cationic protein (ECP) levels in biological samples. It utilizes a fluorescence enzyme immunoassay (FEIA) technique to quantify ECP concentrations.

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2 protocols using phadia immunocap system ecp feia

1

Serum Eosinophil Cationic Protein Measurement

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Serum ECP was measured using the Phadia ImmunoCAP system ECP FEIA (Phadia AB, Uppsala, Sweden), according to the manufacturer's instructions. Briefly, anti-ECP covalently coupled to ImmunoCAP, binds with the ECP in the patient's serum. After washing, enzyme-labeled antibodies against ECP were added to form a complex. After incubation, unbound enzyme-anti-ECP was washed away and the bound complex was then incubated with a developing solution. The reaction was stopped, the fluorescence of the eluate was measured and the response transformed to concentration levels using a calibration curve. The normal range for serum ECP in the patient population that was established in the laboratory was 2.00–15.7 μg/l. Therefore, values above this were considered elevated for the study population. The maximum value was similar to that of a previous study (13.3 μg/l) (37 (link)). To ensure quality control the laboratory participated in an external quality assessment program (Phadia: Quality Club ECP [52-5213-99/05]).
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2

Serum ECP Assessment in Participants

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Serum ECP levels were assessed in all participants following diagnosis. These assessments were conducted using the Phadia ImmunoCAP system ECP FEIA (Phadia AB), in accordance with the manufacturer's instruction. The normal range of serum ECP in the laboratory-established patient population was 2.0–18.0 µg/L [15 (link)].
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