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48 48 access array integrated fluidic circuit ifc  (fluidigm)


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    Structured Review

    fluidigm 48 48 access array integrated fluidic circuit ifc
    48 48 Access Array Integrated Fluidic Circuit Ifc, supplied by fluidigm, used in various techniques. Bioz Stars score: 93/100, based on 843 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/48+48+access+array/Access+Array/pm41761307-103-7-14
    Average 93 stars, based on 843 article reviews
    48 48 access array integrated fluidic circuit ifc - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Polymerase Chain Reaction:

    Article Title: BeeDNA: microfluidic environmental DNA metabarcoding as a tool for connecting plant and pollinator communities
    Article Snippet: As the cost of Illumina sequencing continues to fall, greater sequencing depth can be achieved at equivalent or lower price points (even compared to one year ago) and may ameliorate some of these issues. .. PCR reaction volumes are also much lower using the Fluidigm 48.48 Access ArrayTM (5 μL) than they would be in standard PCR (typically 25 μL or 50 μL). .. Consequently, the amount of template DNA added to Fluidigm 48.48 Access ArrayTM reactions is a fraction of that used in standard PCR reactions, which is problematic as higher volumes of template DNA reduce uncertainty in detection rates ( ).

    Article Title: Molecular identity crisis: environmental DNA metabarcoding meets traditional taxonomy—assessing biodiversity and freshwater mussel populations (Unionidae) in Alabama
    Article Snippet: Briefly, the eDNA was extracted using the inhibitor removing Power Water DNA extraction kit (Qiagen, Hilden, Germany) per manufacturer’s instructions and the samples were cleaned and concentrated post-extraction with the Zymoclean© Large Fragment DNA Recovery Kit (Zymo Research, Irvine, CA, USA). .. Microfluidic high throughput PCR amplification of the eDNA was performed on the Fluidigm 48.48 Access ArrayTM (Fluidigm, San Francisco, CA, USA; ) as previously described in . ..

    Article Title: <scp>BeeDNA</scp> : Microfluidic environmental <scp>DNA</scp> metabarcoding as a tool for connecting plant and pollinator communities
    Article Snippet: .. PCR reaction volumes are also much lower using the Fluidigm 48.48 Access ArrayTM (5 μl) than they would be in standard PCR (typically 25 or 50 μl). .. Consequently, the amount of template DNA added to Fluidigm 48.48 Access ArrayTM reactions is a fraction of that used in standard PCR reactions, which is problematic as higher volumes of template DNA reduce uncertainty in detection rates (Mächler et al., 2015).

    Article Title: <scp>BeeDNA</scp> : Microfluidic environmental <scp>DNA</scp> metabarcoding as a tool for connecting plant and pollinator communities
    Article Snippet: .. The Fluidigm 48.48 Access ArrayTM (Fluidigm Corporation, 2016) was used for PCR amplification of each eDNA sample (2 ng) once with our validated primer panel (see Supporting Information). ..

    High Throughput Screening Assay:

    Article Title: Molecular identity crisis: environmental DNA metabarcoding meets traditional taxonomy—assessing biodiversity and freshwater mussel populations (Unionidae) in Alabama
    Article Snippet: Briefly, the eDNA was extracted using the inhibitor removing Power Water DNA extraction kit (Qiagen, Hilden, Germany) per manufacturer’s instructions and the samples were cleaned and concentrated post-extraction with the Zymoclean© Large Fragment DNA Recovery Kit (Zymo Research, Irvine, CA, USA). .. Microfluidic high throughput PCR amplification of the eDNA was performed on the Fluidigm 48.48 Access ArrayTM (Fluidigm, San Francisco, CA, USA; ) as previously described in . ..

    Amplification:

    Article Title: Molecular identity crisis: environmental DNA metabarcoding meets traditional taxonomy—assessing biodiversity and freshwater mussel populations (Unionidae) in Alabama
    Article Snippet: Briefly, the eDNA was extracted using the inhibitor removing Power Water DNA extraction kit (Qiagen, Hilden, Germany) per manufacturer’s instructions and the samples were cleaned and concentrated post-extraction with the Zymoclean© Large Fragment DNA Recovery Kit (Zymo Research, Irvine, CA, USA). .. Microfluidic high throughput PCR amplification of the eDNA was performed on the Fluidigm 48.48 Access ArrayTM (Fluidigm, San Francisco, CA, USA; ) as previously described in . ..

    Article Title: <scp>BeeDNA</scp> : Microfluidic environmental <scp>DNA</scp> metabarcoding as a tool for connecting plant and pollinator communities
    Article Snippet: Consequently, the amount of template DNA added to Fluidigm 48.48 Access ArrayTM reactions is a fraction of that used in standard PCR reactions, which is problematic as higher volumes of template DNA reduce uncertainty in detection rates (Mächler et al., 2015). .. In our study, 2 ng of template DNA was loaded to the Fluidigm 48.48 Access ArrayTM, providing 0.13 ng DNA for amplification with each primer set in each reaction chamber. ..

    Article Title: <scp>BeeDNA</scp> : Microfluidic environmental <scp>DNA</scp> metabarcoding as a tool for connecting plant and pollinator communities
    Article Snippet: .. The Fluidigm 48.48 Access ArrayTM (Fluidigm Corporation, 2016) was used for PCR amplification of each eDNA sample (2 ng) once with our validated primer panel (see Supporting Information). ..



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