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Ridascreen

Manufactured by R-Biopharm
Sourced in Germany

RIDASCREEN is a quantitative enzyme-linked immunosorbent assay (ELISA) test kit designed for the detection and measurement of various analytes in samples. The kit provides the necessary components and protocols to perform the ELISA procedure, enabling accurate and reliable quantification of the target analyte.

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22 protocols using ridascreen

1

Diagnosing Mycoplasma Pneumoniae Infection

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Blood tests for measuring peripheral WBC counts, and CRP, LDH, and mycoplasma IgM antibody levels were performed on admission. A blood test for measuring mycoplasma IgM antibody level was performed within 7 days after admission for diagnosing MPP.
A serum sample for PCT level determination was collected on admission and stored at -20°C until analyzed. Serum PCT level was measured on a Roche Cobas e601 analyzer based on an electrochemiluminescence immunoassay using the Elecsys BRAHMS PCT kit (Roche Diagnostics Korea, Seoul, Korea). The assay detection range was 0.02–100 ng/mL.
Serum mycoplasma IgM level was assayed using an enzyme immunoassay (RIDASCREEN; R-Biopharm AG, Darmstadt, Germany). The cutoff level for mycoplasma IgM antibody level was 71 U/mL. Mycoplasma PCR of sputum or nasopharyngeal aspiration samples was performed using the Bio-Core M. pneumoniae PCR Kit (Seegene, Seoul, Korea). The mycoplasma PCR was performed in 2 patients, and those patients showed positive results in both PCR and serology tests. PCR was not performed in the remaining patients, and the diagnosis was established using the enzyme immunoassay (EIA) method.
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2

Serological Testing for B19V Antibodies

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When necessary (i.e. for samples without previous determination of B19V-specific IgM and/or IgG), anti-B19V antibodies were determined using enzyme-linked immunosorbent assays (Ridascreen, R-biopharm), following the manufacturer’s instructions. For IgM assay serum, samples were treated with RIDA RF-Absorbens (R-biopharm) for the precipitation of IgG antibodies.
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3

Elemental Analysis of Milk and Serum

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Inductively coupled plasma mass spectrometry analysis was used to quantify concentrations of quantity elements (Na, Mg, P, K, and Ca), essential trace elements (V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Mo, and I), and heavy metals (Cd, Hg, and Pb) in milk and serum. For measurement of vitamin B12 in undiluted milk, a commercial competitive assay (RIDAscreen, R-Biopharm) was used. Analyses were carried out according to the methods previously published by our group (Denholm et al., 2019 (link)).
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4

Gluten-Free Bread Gluten Analysis

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To ensure the gluten content remained below the required threshold (<3 ppm), gluten analysis was conducted on the prepared bread. To accurately measure gluten levels, specialized testing methods such as Ridascreen Gliadin (R-Biopharm AG, Darmstadt, Germany); Veratox for Gliadin R5 (Neogen, Lansing, Michigan, USA); and AgraQuant Gluten G12 (Romer Labs, Getzersdorf, Austria) were used. All values were designated as mean ± standard deviation (n = 3).
The gluten content in the gluten-free bread product was analyzed using the gliadin test Ridascreen (R-Biopharm AG, Darmstadt, Germany), which was also used by Ja Myung Yu [64 (link)].
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5

Inflammatory Biomarkers in Stool and Blood

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Blood samples and stool specimens were collected within 24 hours of admission. Blood inflammatory biomarkers including highly sensitive C-reactive protein (Beckman Coulter, Inc., Brea, CA, USA), erythrocyte sedimentation rate (ESR) (TEST-1; Alifax, Polverara, Italy), and leukocytes from complete blood count (CBC) (Sysmex, Kobe, Japan), and fecal inflammatory biomarkers including calprotectin (Ridascreen®; R-Biopharm, Darmstadt, Germany), lactoferrin (Abcam; Cambridge, UK), MPO (Abcam), and PMN-e (Abcam) were assessed quantitatively. Fecal leukocytes were examined using microscopy. An average number of leukocytes that was ≥1/high power field was considered positive. Fecal occult blood was examined by an immunochemical occult blood test (OC-Sensor Diana; Eiken Chemical Co., Ltd. Tokyo, Japan). A result that was ≥100 ng/mL was considered positive.
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6

Blood Biomarkers for Toxocara Exposure

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One milliliter of blood from all the participants was added to the biochemical tube to perform ferritin, 25(OH)D, and Toxocara canis determination. Ferritin and 25(OH)D concentrations were analyzed at the biochemistry laboratory of the Germans Trias i Pujol Hospital (Badalona, Spain) with a Chemiluminescence Immunoassay (CLIA) method using a Liaison instrument (DiaSorin Liaison, Stillwater, MN, United States). 25(OH)D is an indirect method to measure vitamin D in the blood. According to the literature, serum 25(OH)D levels equal or above 20 ng/ml were considered normal levels of vitamin D (Michael and Holick, 2007 (link)). To avoid variations during blood sampling, the blood was almost always collected on the same day of the week at approximately the same hour (13–15 h). Seasonal fluctuations did not affect sampling because the weather seasons in Haiti are barely defined. T. canis Ig-G antibodies were detected at the IGTP laboratory using a commercial ELISA kit (Ridascreen, R-Biopharm AG, Germany). Results with a sample index above 1.1 were considered positive according to the manufacturer’s instructions.
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7

Optimized Gluten Extraction Method

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For comparison experiments we used both R5-based (Ridascreen, R-Biopharm AG, Darmstadt, Germany) and G12 (AgraQuant, Romer Labs, Runcorn, UK) ELISA kits. Commercial extraction procedures were replaced with an in-house modified extraction method based on cocktail and ethanol combination, which is described below. The extracts were assayed simultaneously in parallel with three test kits: G12-, R5- and X6-based according to the procedure given in Table 2.
Food samples were milled in a food grinder (J500, Bork, Moscow, Russia). A total of 0.25 g of homogenized material was mixed with 2.5 mL of patented Mendez cocktail solution (EP 2003448 A1) (2-M GuHCl + 0.25-M 2ME in PBS, pH 7.3). The mixtures were incubated in a water bath (Biosan) at 50 °C for 40 min. After the incubation was completed 7.5 mL of 80% ethanol was added to the samples and prolamin fraction was solubilized for 1 h at room temperature. The samples were centrifuged at 4000× g (Eppendorf, Hamburg, Germany) for 10 min. For further analysis, the extracts obtained were used according to the procedure, described in Table 2.
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8

Fecal Calprotectin Quantification by ELISA

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The FCP concentration was measured using a quantitative enzyme-linked immunosorbent assay (RIDASCREEN®; R-Biopharm AG, Darmstadt, Germany). All fecal samples were processed within 72 hours of collection. Fecal specimens were diluted to 1:2,500. Enzyme-linked immunosorbent assay (ELISA) plates were read using a Spectra Mini Reader. According to the manufacturer’s instructions, samples containing ≥ 50 mg/kg feces were considered calprotectin positive [20 (link),21 (link)].
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9

ELISA Kit for Histamine Quantification

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An enzyme-linked immunosorbent assay (ELISA) kit for histamine determination (RIDASCREEN®) was provided by R-Biopharm (Darmstadt, Germany). All reagents were included in the commercial kit and the assay was performed following the manufacturer’s instructions.
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10

Assay Kits for TNF-Alpha Inhibitors

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Commercial laboratories have developed various assay procedures for TNF alpha inhibitors and antibodies against TNF alpha inhibitors. The LISA TRACKER (Theradiag, Croissy-Beaubourg, France), (Immundiagnostik/BioHit Healthcare, Bensheim, Germany), Promonitor (Grifols Diagnostic Solutions, Emeryville, United States) and RIDASCREEN (R-Biopharm, Darmstadt, Germany) are particular examples of these essays classed as solid-phase ELISAs. They are intended to be used for measuring the levels of TNF alpha inhibitors and antibodies against TNF alpha inhibitors in the blood of people having treatment with biologics for Crohn disease. However, these kits vary in designs and there is a lack of standardization. Their unique features are detailed in the following (see Tables 1 and 2).
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