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multichannel elisa reader  (Tecan Systems)


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    Structured Review

    Tecan Systems multichannel elisa reader
    Multichannel Elisa Reader, supplied by Tecan Systems, used in various techniques. Bioz Stars score: 99/100, based on 10445 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/multichannel+elisa+reader/Sunrise/pmc09250970__DataSheet1-42-21-24
    Average 99 stars, based on 10445 article reviews
    multichannel elisa reader - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Antibody recognition in multiple sclerosis and Rett syndrome using a collection of linear and cyclic N-glucosylated antigenic probes.
    Article Snippet: After 3 h at room temperature incubation and three washes, 100 mL of substrate solution consisting of 1 mg/mL p-nitrophenyl phosphate (SigmaAldrich, Milan, Italy) in 10% diethanolamine buffer (pH 9.8) were added. .. After 30 min, the reaction was stopped with 1M NaOH (50 mL/well), and the absorbance was read in a multichannel ELISA reader (Tecan Sunrise, M€annedorf, Switzerland) at 405 nm (reference filter 650 nm). ..

    Article Title: Glucopeptides derived from myelin-relevant proteins and hyperglucosylated nontypeable Haemophilus influenzae bacterial adhesin cross-react with multiple sclerosis specific antibodies: A step forward in the identification of native autoantigens in multiple sclerosis.
    Article Snippet: Interdepartmental Research Unit of Peptide and Protein Chemistry and Biology, Department of Chemistry “Ugo Schiff”, University of Florence, Sesto Fiorentino, Italy Institute of Chemistry of Organometallic Compounds (ICCOM), National Research Council of Italy (CNR), Sesto Fiorentino, Italy University of Burgos, Burgos, Spain Department of Pharmacy, University of Naples “Federico II”, Naples, Italy Interdepartmental Research Unit of Peptide and Protein Chemistry and Biology, Department of NeuroFarBa, University of Florence, Sesto Fiorentino, Italy

    Article Title: Role of Helical Structure in MBP Immunodominant Peptides for Efficient IgM Antibody Recognition in Multiple Sclerosis
    Article Snippet: Colorimetric reaction was carried out adding 100 μl of substrate reaction solution (1 mg/ml p NPP, MgCl 2 0.01 M in carbonate buffer, pH 9.6) to each well and plates were read at 405 nm using a TECAN plate reader. .. After 30 min, the reaction was stopped with 1 M NaOH solution (50 μL/well) and the absorbance was read in a multichannel ELISA reader (Tecan Sunrise, Männedorf, Switzerland) at 405 nm. ..

    Article Title: MBP Peptides for Antibody Recognition
    Article Snippet: Colorimetric reaction was carried out adding 100 μl of substrate reaction solution (1 mg/ml pNPP, MgCl2 0.01M in carbonate buffer, pH 9.6) to each well and plates were read at 405 nm using a TECAN plate reader. .. After 30 min, the reaction was stopped with 1 M NaOH solution (50 μL/well) and the absorbance was read in a multichannel ELISA reader (Tecan Sunrise, Männedorf, Switzerland) at 405 nm. ..

    Article Title: Role of Helical Structure in MBP Immunodominant Peptides for Efficient IgM Antibody Recognition in Multiple Sclerosis.
    Article Snippet: The microplates were then incubated 3 h at room temperature and, after washes (3×), 100 μL of substrate solution consisting of 1 mg/ml p-nitrophenyl phosphate pNPP (Merck, Milan, Italy) and MgCl2 0.01 M in carbonate buffer (pH 9.6) were added. .. After approximately 30 min, the reaction was stopped with 1 M NaOH solution (50 μL/well), and the absorbance was read in a multichannel ELISA reader (Tecan Sunrise, Männedorf, Switzerland) at 405 nm. ..

    Article Title: Role of Helical Structure in MBP Immunodominant Peptides for Efficient IgM Antibody Recognition in Multiple Sclerosis.
    Article Snippet: Colorimetric reaction was carried out adding 100 μl of substrate reaction solution (1 mg/ml pNPP, MgCl2 0.01 M in carbonate buffer, pH 9.6) to each well and plates were read at 405 nm using a TECAN plate reader. .. After 30 min, the reaction was stopped with 1 M NaOH solution (50 μL/well) and the absorbance was read in a multichannel ELISA reader (Tecan Sunrise, Männedorf, Switzerland) at 405 nm. ..

    Article Title: Role of Helical Structure in MBP Immunodominant Peptides for Efficient IgM Antibody Recognition in Multiple Sclerosis
    Article Snippet: The microplates were then incubated 3 h at room temperature and, after washes (3×), 100 μL of substrate solution consisting of 1 mg/ml p-nitrophenyl phosphate pNPP (Merck, Milan, Italy) and MgCl 2 0.01 M in carbonate buffer (pH 9.6) were added. .. After approximately 30 min, the reaction was stopped with 1 M NaOH solution (50 μL/well), and the absorbance was read in a multichannel ELISA reader (Tecan Sunrise, Männedorf, Switzerland) at 405 nm. ..

    Article Title: Epitope mapping of anti-myelin oligodendrocyte glycoprotein (MOG) antibodies in a mouse model of multiple sclerosis: microwave-assisted synthesis of the peptide antigens and ELISA screening.
    Article Snippet: The role of pathologic auto-antibodies against myelin oligodendrocyte glycoprotein (MOG) in multiple sclerosis is a highly controversial matter.. As the use of animal models may enable to unravel the molecular mechanisms of the human disorder, numerous studies onmultiple sclerosis are carried out using experimental autoimmune encephalomyelitis (EAE).. In particular, the most extensively used EAE model is obtained by immunizing C57BL/6 mice with the immunodominant peptide MOG(35–55).

    Incubation:

    Article Title: Epitope mapping of anti-myelin oligodendrocyte glycoprotein (MOG) antibodies in a mouse model of multiple sclerosis: microwave-assisted synthesis of the peptide antigens and ELISA screening.
    Article Snippet: The role of pathologic auto-antibodies against myelin oligodendrocyte glycoprotein (MOG) in multiple sclerosis is a highly controversial matter.. As the use of animal models may enable to unravel the molecular mechanisms of the human disorder, numerous studies onmultiple sclerosis are carried out using experimental autoimmune encephalomyelitis (EAE).. In particular, the most extensively used EAE model is obtained by immunizing C57BL/6 mice with the immunodominant peptide MOG(35–55).



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