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Human crp quantikine elisa kit

Manufactured by R&D Systems
Sourced in United States

The Human CRP Quantikine ELISA Kit is an in vitro enzyme-linked immunosorbent assay (ELISA) designed for the quantitative measurement of human C-reactive protein (CRP) levels in serum, plasma, and cell culture supernatants.

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7 protocols using human crp quantikine elisa kit

1

Plasma Protein Validation by ELISA

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To further validate the identified DEPs, ELISA was performed to measure plasma proteins concentrations according to the manufacturer’s instructions. The concentrations of C-reactive protein (CRP), heat shock protein beta-1 (HSPB1), vinculin (VINC) and growth/differentiation factor 15 (GDF15) were respectively quantified using a Human CRP Quantikine ELISA Kit (DCRP00, R&D Systems), HSPB1 Human ELISA Kit (EHHSPB1, Thermo Fisher Scientific), Human Vinculin ELISA Kit (LS-F34925, LifeSpan Biosciences) and Human GDF15 ELISA Kit (KIT10936, Sino Biological).
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2

Standardized ELISA Methods for CRP and MIA

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For C-reactive protein, or CRP, and melanoma inhibitory activity protein, or MIA, ELISAs were used in the Validation Cohort. For CRP, we used the Human CRP Quantikine ELISA Kit (R&D CDRP00), diluting plasma samples 1:200. For MIA, we used the MIA ELISA Kit (Roche 11976826001), diluting plasma samples 1:2.
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3

Quantitative Determination of Inflammatory Biomarkers

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The method used for the quantitative determination of CRP, IL-1β and SDF-1α was the enzyme-linked immunosorbent assay (ELISA) method. The protocol for each of the three ILs was performed following the instructions of R&D Systems Human Kit designated for each cytokine in part (Human CRP Quantikine ELISA Kit, IL-1β Human IL-1β/IL-1β F2 Quantikine ELISA Kit and Human CXCL12/SDF-1α Quantikine ELISA Kit, R&D Systems Inc., Minneapolis, MN). The normal range of values for CRP was between 1.09 and 4.291 mg/L, with a mean of 1.769 mg/L, with the limit of detection 0.005–0.022 ng/mL (mean value 0.010 ng/mL) and no significant cross-reactivity or interference; the coefficient of variance for intra-assay precision was 3.8–4.3% and for inter-assay precision 6–7%. For IL-1β, the normal range of values was between 1 and 3.9 pg/mL, with the limit of detection 1 pg/mL and no significant cross-reactivity or interference; the coefficient of variance for intra-assay precision was in the range 2.8–8.5% and for inter-assay precision, 4.1–8.4%. For SDF-1α, the normal range of values was between 1330 and 2720 pg/mL (mean 1830 pg/mL), with the limit of detection 1.0–47 pg/mL (mean value 18 pg/mL) and no significant cross-reactivity or interference; the coefficient of variance for intra-assay precision was between 3.4% and 3.9% and for inter-assay precision, 8.2–13.4%
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4

CISD2, IL6, and CRP Quantification in CNS Insults

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The plasma and CSF levels of CISD2, IL6, and CRP in patients with CNS insults were examined using human CISD2 ELISA kit (catalog: MBS7244473, MyBiosource, San Diego, CA, USA), human IL-6 Quantikine ELISA kit (catalog: D6050, R&D Systems, Minneapolis, MN, USA), and human CRP Quantikine ELISA kit (catalog: DCRP00, R&D Systems), respectively, whereas the brain levels of Tnfa in SCI mice were examined using a DuoSet® mouse TNF-α ELISA kit (Catalog: DY410, R&D Systems). Briefly, 300 μL human plasma or CSF samples or mouse brain tissue lysates diluted (1:100) in lysis buffer were subjected to the immunoassay, following the manufacturer’s instructions. The standards of the target protein were analyzed in duplicates, whereas the samples were analyzed in triplicates. At least three independent human samples and six independent mouse samples were used for the analysis.
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5

Plasma BDNF and Cytokine Measurement

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Plasma BDNF levels were measured using a BDNF Kit (Quantikine Human BDNF kit; R&D Systems, Minneapolis, MN, USA) (www.RnDSystems.com) and an ELISA reader with a minimum detectable dose of 80 pg/mL (SpectraMax-M2; Molecular Devices, Sunnyvale, CA, USA). All samples were analyzed twice. The cytokine ELISA kits used were also purchased from R&D systems and included a Human CRP Quantikine ELISA Kit, a Human TNF-alpha Quantikine ELISA Kit, and a Human IL-8 Quantikine ELISA Kit for the assessment of plasma levels of CRP, TNF-α, and IL-8, respectively.
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6

Quantitative Determination of Inflammatory Biomarkers

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The method used for the quantitative determination of CRP, IL-1β and SDF-1α was the enzyme-linked immunosorbent assay (ELISA) method. The protocol for each of the three ILs was performed following the instructions of R&D Systems Human Kit designated for each cytokine in part (Human CRP Quantikine ELISA Kit, IL-1β Human IL-1β/IL-1β F2 Quantikine ELISA Kit and Human CXCL12/SDF-1α Quantikine ELISA Kit, R&D Systems Inc., Minneapolis, MN). The normal range of values for CRP was between 1.09 and 4.291 mg/L, with a mean of 1.769 mg/L, with the limit of detection 0.005–0.022 ng/mL (mean value 0.010 ng/mL) and no significant cross-reactivity or interference; the coefficient of variance for intra-assay precision was 3.8–4.3% and for inter-assay precision 6–7%. For IL-1β, the normal range of values was between 1 and 3.9 pg/mL, with the limit of detection 1 pg/mL and no significant cross-reactivity or interference; the coefficient of variance for intra-assay precision was in the range 2.8–8.5% and for inter-assay precision, 4.1–8.4%. For SDF-1α, the normal range of values was between 1330 and 2720 pg/mL (mean 1830 pg/mL), with the limit of detection 1.0–47 pg/mL (mean value 18 pg/mL) and no significant cross-reactivity or interference; the coefficient of variance for intra-assay precision was between 3.4% and 3.9% and for inter-assay precision, 8.2–13.4%
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7

Quantifying Serum C-Reactive Protein

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Serum levels of C-reactive protein (CRP) were measured using a human CRP quantikine ELISA Kit (DCRP00, R&D Systems). All operations were performed in strict accordance with manufacturer's instructions. Serum levels of CRP were normalized to mg/L.
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