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custom multiplex genotyping panel on a matrix-assisted laser desorption/ionization time-of-flight (maldi-tof) mass spectrometry platform massarray  (agena bioscience)


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    agena bioscience custom multiplex genotyping panel on a matrix-assisted laser desorption/ionization time-of-flight (maldi-tof) mass spectrometry platform massarray
    Custom Multiplex Genotyping Panel On A Matrix Assisted Laser Desorption/Ionization Time Of Flight (Maldi Tof) Mass Spectrometry Platform Massarray, supplied by agena bioscience, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/massarray+multiplex+genotyping+platform/custom+multiplex+genotyping+panel+on+a+matrix+assisted+laser+desorption++ionization+time+of+flight++maldi+tof++mass+spectrometry+platform/pm40379588-56-22-30
    Average 90 stars, based on 1 article reviews
    custom multiplex genotyping panel on a matrix-assisted laser desorption/ionization time-of-flight (maldi-tof) mass spectrometry platform massarray - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Mass Spectrometry:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t

    Sequencing:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t

    Amplification:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t

    Multiplex Assay:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t

    DNA Sequencing:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t

    Control:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t

    Software:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t

    Significance Assay:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t

    Polymerase Chain Reaction:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t

    Biomarker Discovery:

    Article Title: Development of mass spectrometry-based genotyping method for simultaneous detection of 35 HPA systems, 5 HNA systems and the CD36 antigen.
    Article Snippet: MS) technology. Study Design and Methods: Specific primers for amplification and single-base extension were designed, distributing 53 loci into two multiplex pools. Genotyping was performed using the MassARRAY MS platform. Method accuracy was verified by Sanger sequencing for all 53 loci (34 samples) and flow cytometric serotyping for HPA-1, -3, -5 and CD36. The validated method was then applied t



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