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multi detector microplate reader  (Tecan Systems)


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    Tecan Systems multi detector microplate reader
    Multi Detector Microplate Reader, supplied by Tecan Systems, used in various techniques. Bioz Stars score: 99/100, based on 17018 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/multi+detector+microplate+reader/Spark/pm39970570-115-6-10
    Average 99 stars, based on 17018 article reviews
    multi detector microplate reader - by Bioz Stars, 2026-09
    99/100 stars

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    other:

    Article Title: A new technique for antioxidant walnut peptide preparation directly from walnut cake: Enzymatic preparation process optimization coupled with enzyme membrane reactor and kinetic analysis.
    Article Snippet: The lack of scalable production methods limits the commercial production viability of walnut peptides.. To overcome this obstacle, enzyme membrane reactors (EMRs) were used to continuously produce bioactive peptides (called CEMR) directly from walnut cake.. The optimum operating conditions were pH 10.7, an [E/S] ratio of 11 %, and a temperature of 44 C, which resulted in a peptide yield of 256.0 ± 4.66 mg/g cake and a protein conversion degree reaching 63.49 ± 0.82 %.



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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 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