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multi detector microplate reader  (Danaher Inc)


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    Danaher Inc multi detector microplate reader
    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.
    Multi Detector Microplate Reader, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 17664 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/multi detector microplate reader/product/Danaher Inc
    Average 99 stars, based on 17664 article reviews
    multi detector microplate reader - by Bioz Stars, 2026-06
    99/100 stars

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    1) Product Images from "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."

    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.

    Journal: Viruses

    doi: 10.3390/v17050656

    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.
    Figure Legend 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.

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



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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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    Image Search Results


    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