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Human d dimer elisa kit

Manufactured by Abcam
Sourced in United Kingdom

The Human D-dimer ELISA kit is a quantitative enzyme-linked immunosorbent assay (ELISA) designed to measure D-dimer levels in human samples. D-dimer is a protein fragment that is released into the bloodstream when a blood clot is broken down. This kit provides the necessary reagents and materials to perform the D-dimer ELISA test.

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4 protocols using human d dimer elisa kit

1

Biomarker Dynamics in COVID-19 Patients

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The concentrations of serum D-dimer, C-reactive protein, ferritin, cardiac troponin I and interleukin 6 were determined with a human D-dimer ELISA kit, a human CRP ELISA kit, a human ferritin ELISA kit, a human cardiac troponin I ELISA kit and an IL-6 ELISA kit (Abcam, Cambridge, UK) measured on a PHOmo microplate reader (Autobio Diagnostics, Zhengzhou, China) according to the manufacturer's instructions. For hospitalized patients, day 1, day 7, day 14 and day 28 samples were used, while for ambulatory patients, day 1, day 14 and day 28 were used. The detection limits for D-dimer, C-reactive protein, ferritin, cardiac troponin I and interleukin 6 were 2.36 ng/mL, 5.36 pg/mL, 5 ng/mL, 4.4 pg/mL and 3 pg/mL respectively.
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2

Quantifying Plasma Coagulation Markers

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We assessed plasma samples by using commercially available kits. For plasminogen activator inhibitor 1 (PAI-1) we used Human Serpin E1/PAI-1 Quantikine ELISA Kit (R&D Systems, https://www.rndsystems.com) or Human PAI-1 Platinum Kit (eBioscience, https://www.thermofisher.com). We used Human t-Plasminogen Activator/tPA Quantikine ELISA Kit (R&D Systems) to measure tissue plasminogen activator (tPA). We used Human Thrombomodulin/BDCA-3 Quantikine ELISA Kit (R&D Systems) or Human Thrombomodulin ELISA Kit (Innovative Research Inc., https://www.innov-research.com) to measure thrombomodulin (THBD) and Human Thrombin-Antithrombin Complex ELISA Kit (Abcam, https://www.abcam.com) to measure thrombinantithrombin (TAT) complexes. To assess endothelial protein C receptor (EPCR) we used Human EPCR DuoSet ELISA Kit (R&D Systems), for D-dimer we used Human D-Dimer ELISA Kit (Abcam), for a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS-13) we used Human ADAMTS13 Quantikine ELISA Kit (R&D Systems), for P-selectin we used Human CD62P ELISA Kit (Abcam), for hepatocyte growth factor (HGF) we used Human HGF Quantikine ELISA Kit (R&D Systems), for von Willebrand factor (vWF) we used vWF Human ELISA Kit (ThermoFisher, https://www.thermofisher.com), and for tissue factor we used Human Coagulation Factor III/Tissue Factor Quantikine ELISA Kit (R&D Systems).
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3

Biomarkers and Cardiac Function Assessment

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We drew blood samples from a brachial vein in all patients upon admission. Blood was collected in EDTA tubes. After centrifuged (3000 g/min for 10 min), plasma and plasma aliquots were stored at −80°C freezer. Upon thawing from the freezer, samples were applied to experiments immediately. The D-dimer was measured by the human D-dimer ELISA kit (ab196269, Abcam, Cambridge, MA, USA) with a sensitivity of 71 pg/mL. We quantified the ET-1 level by an Endothelin-1 ELISA Kit (ab133030, Abcam, Cambridge, MA, USA) with a sensitivity of 0.41 pg/mL. The C-reactive protein, creatine kinase (CK), CK-MB, and troponin T plasma levels were measured every 4 hours during the first day and every 24 hours in the following 3 days using routine methods. The LV ejection fraction was quantified within 2 hours after the PCI procedure by 2D-echocardiography (Simpson method).
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4

Soluble Biomarkers in Coagulation and Inflammation

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Soluble fibrinogen and soluble P-selectin levels were determined in plasma using the human fibrinogen ELISA kit and human P-selectin/CD62P DuoSet ELISA kit (R&D Systems, Minneapolis, MN, USA), respectively. D-dimer, high-sensitivity interleukin-6 (hsIL-6) and C-reactive protein were determined with the human D-dimer ELISA kit (Abcam, Cambridge, UK), human hsIL-6 Quantikine ELISA kit (R&D Systems) and human C-reactive protein ELISA kit (R&D Systems), respectively. For platelet content, whole blood was centrifuged for 15 min at 156 g without break to obtain platelet-rich plasma. Platelet concentration was adjusted to 300 × 10 9 /L by addition of autologous plasma. Samples were freeze-thawed for 3 cycles to fragment the platelets, followed by ultra-centrifugation for 5 min at 5,000 rpm to spin down large particles, and supernatants were taken for ELISA. Platelet fibrinogen and P-selectin were determined with the ELISA kits described above.
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