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Liblia hfabp latex agglutination turbidimetric immunoassay

Manufactured by Sumitomo Pharma
Sourced in Japan

LIBLIA HFABP is a latex agglutination turbidimetric immunoassay used for the quantitative determination of heart-type fatty acid-binding protein (HFABP) in human serum or plasma samples. The assay principle involves the agglutination of latex particles coated with anti-HFABP antibodies upon reaction with HFABP in the sample, which is measured turbidimetrically.

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2 protocols using liblia hfabp latex agglutination turbidimetric immunoassay

1

Biomarker Measurement in Acute Kidney Injury

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The urine and blood samples were collected within 30 min of admission. The urine and blood samples were centrifuged within 5 min at 4°C and immediately frozen at −80°C until they were analysed. The serum levels of HFABP, hsTnT, NT‐proBNP, and BNP were measured on admission. In addition, the urine NGAL, LFABP, β2MG, NAG, and albumin excretion were also measured on admission. These urine and serum biomarkers were measured by the Special Reference Laboratory (SRL©, Tokyo, Japan). The level of urine LFABP was measured with an enzyme‐linked immunosorbent assay (ELISA) using a human LFABP ELISA Kit (Kyowa Medex Co., Tokyo, Japan). The level of urinary NGAL was measured using the NGAL ELISA Kit (R&D Systems, Inc., Minneapolis, MN). The serum HFABP was measured using a MARKIT‐M HFABP ELISA Kit until June 2012 and using a LIBLIA HFABP latex agglutination turbidimetric immunoassay from July 2012 (DS Pharma Biomedical, Osaka, Japan). The lower and upper limits of detection for the urinary NGAL concentration were 4 and 500 pg/mL, respectively, and the lower limit for the urine LFABP was 2.9 pg/mL.
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2

Biomarker Measurement in Heart Disease

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The blood samples were collected in tubes within 10 min of admission and centrifuged within 30 min after admission. The serum levels of hs-TropT, Nt-proBNP, and HFABP were measured additionally using standard laboratory parameters via standard enzymatic methods: an electrochemiluminescence immunoassay (Roche Diagnostics Ltd, Rotkreuz, Switzerland), a chemiluminescent immunoassay (CLEIA), and a MARKIT-M HFABP enzyme-linked immunosorbent assay kit or LIBLIA H-FABP latex agglutination turbidimetric immunoassay (DS Pharma Biomedical, Osaka, Japan). The measurements of these biomarkers were obtained in all 1183 patients. The lower limit of detection for the serum concentration of HFABP was 1.0 ng/mL, while that of hs-TropT was 3 ng/L.
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