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detector antibody  (R&D Systems)


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    Structured Review

    R&D Systems detector antibody
    Detector Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/detector antibody/product/R&D Systems
    Average 94 stars, based on 21 article reviews
    detector antibody - by Bioz Stars, 2026-05
    94/100 stars

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    Figure 4. Fluorescent focus unit reduction-based assay for detection of neutralizing antibodies against PRRSV. The fluorescent focus unit reduction-based assay was performed using rPRRSV-SH01-eGFP at a dose of 100 TCID50 and serum samples diluted from 1:4 to 1:64. The fluorescent foci were captured using a multi-detector <t>microplate</t> reader at 48 h post-inoculation. (A) Green fluorescence of the tested samples was visualized under an inverted fluorescence microscope. Scale bar: 200 µm. (B) Fluorescent focus units of the serum samples from vaccinated pigs. (C) Fluorescent focus units of the serum samples from naïve pigs. Data are expressed as the mean ± standard deviation (SD). V, cells infected with rPRRSV-SH01-eGFP alone as a virus control; M, mock-infected cells as a negative control.
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    R&D Systems detector antibody
    Figure 4. Fluorescent focus unit reduction-based assay for detection of neutralizing antibodies against PRRSV. The fluorescent focus unit reduction-based assay was performed using rPRRSV-SH01-eGFP at a dose of 100 TCID50 and serum samples diluted from 1:4 to 1:64. The fluorescent foci were captured using a multi-detector <t>microplate</t> reader at 48 h post-inoculation. (A) Green fluorescence of the tested samples was visualized under an inverted fluorescence microscope. Scale bar: 200 µm. (B) Fluorescent focus units of the serum samples from vaccinated pigs. (C) Fluorescent focus units of the serum samples from naïve pigs. Data are expressed as the mean ± standard deviation (SD). V, cells infected with rPRRSV-SH01-eGFP alone as a virus control; M, mock-infected cells as a negative control.
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    Image Search Results


    The 1 μL sample volume with 5 μL AuNPs’ conjugated mAbs and 54 μL running buffer calibration curves in ( a ) OD values’ optimisation in regard to OD 10, OD 5, OD 2.5; ( b ) calibration curves with CN 95, CN 110, and CN140 (OD 5 AuNPs).

    Journal: Biosensors

    Article Title: Performance of Colorimetric Lateral Flow Immunoassays for Renal Function Evaluation with Human Serum Cystatin C

    doi: 10.3390/bios15070445

    Figure Lengend Snippet: The 1 μL sample volume with 5 μL AuNPs’ conjugated mAbs and 54 μL running buffer calibration curves in ( a ) OD values’ optimisation in regard to OD 10, OD 5, OD 2.5; ( b ) calibration curves with CN 95, CN 110, and CN140 (OD 5 AuNPs).

    Article Snippet: A λ is the absorbance at the wavelength λ [ ]. (1) O D λ = A λ L = 1 L log 10 I 0 I In total, 40 OD AuNPs (40 nm, ab269942, Abcam, Cambridge, UK) were conjugated with the 89.5 μg/mL detector mAbs (Fitzgerald, 10-7887, Stratech, Ely, UK).

    Techniques:

    Figure 4. Fluorescent focus unit reduction-based assay for detection of neutralizing antibodies against PRRSV. The fluorescent focus unit reduction-based assay was performed using rPRRSV-SH01-eGFP at a dose of 100 TCID50 and serum samples diluted from 1:4 to 1:64. The fluorescent foci were captured using a multi-detector microplate reader at 48 h post-inoculation. (A) Green fluorescence of the tested samples was visualized under an inverted fluorescence microscope. Scale bar: 200 µm. (B) Fluorescent focus units of the serum samples from vaccinated pigs. (C) Fluorescent focus units of the serum samples from naïve pigs. Data are expressed as the mean ± standard deviation (SD). V, cells infected with rPRRSV-SH01-eGFP alone as a virus control; M, mock-infected cells as a negative control.

    Journal: Viruses

    Article Title: The Junction Between nsp1β and nsp2 in the Porcine Reproductive and Respiratory Syndrome Virus Genome Is a New Site for the Insertion and Expression of Foreign Genes.

    doi: 10.3390/v17050656

    Figure Lengend Snippet: Figure 4. Fluorescent focus unit reduction-based assay for detection of neutralizing antibodies against PRRSV. The fluorescent focus unit reduction-based assay was performed using rPRRSV-SH01-eGFP at a dose of 100 TCID50 and serum samples diluted from 1:4 to 1:64. The fluorescent foci were captured using a multi-detector microplate reader at 48 h post-inoculation. (A) Green fluorescence of the tested samples was visualized under an inverted fluorescence microscope. Scale bar: 200 µm. (B) Fluorescent focus units of the serum samples from vaccinated pigs. (C) Fluorescent focus units of the serum samples from naïve pigs. Data are expressed as the mean ± standard deviation (SD). V, cells infected with rPRRSV-SH01-eGFP alone as a virus control; M, mock-infected cells as a negative control.

    Article Snippet: The fluorescence signal of each well was read on a multi-detector microplate reader (SpectraMax M3; Molecular Devices, San Jose, CA, USA) at Ex/Em = 485/535 nm at 48 h post-inoculation.

    Techniques: Microscopy, Standard Deviation, Infection, Virus, Control, Negative Control