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nebuffer 2 1 concentration  (New England Biolabs)


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    Structured Review

    New England Biolabs nebuffer 2 1 concentration
    Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.
    Nebuffer 2 1 Concentration, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 765 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/nebuffer 2 1 concentration/product/New England Biolabs
    Average 96 stars, based on 765 article reviews
    nebuffer 2 1 concentration - by Bioz Stars, 2026-04
    96/100 stars

    Images

    1) Product Images from "Development and Laboratory Validation of a Field‐Deployable CRISPR ‐Cas12a eDNA Assay for Phylogeographic Lineage Detection in Arctic Char ( Salvelinus alpinus )"

    Article Title: Development and Laboratory Validation of a Field‐Deployable CRISPR ‐Cas12a eDNA Assay for Phylogeographic Lineage Detection in Arctic Char ( Salvelinus alpinus )

    Journal: Molecular Ecology Resources

    doi: 10.1111/1755-0998.70125

    Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.
    Figure Legend Snippet: Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.

    Techniques Used: Titration, Concentration Assay, CRISPR



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    96
    New England Biolabs nebuffer 2 1 concentration
    Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.
    Nebuffer 2 1 Concentration, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/nebuffer 2 1 concentration/product/New England Biolabs
    Average 96 stars, based on 1 article reviews
    nebuffer 2 1 concentration - by Bioz Stars, 2026-04
    96/100 stars
      Buy from Supplier

    96
    New England Biolabs nebuffer 2 1 concentrations
    Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.
    Nebuffer 2 1 Concentrations, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/nebuffer 2 1 concentrations/product/New England Biolabs
    Average 96 stars, based on 1 article reviews
    nebuffer 2 1 concentrations - by Bioz Stars, 2026-04
    96/100 stars
      Buy from Supplier

    96
    New England Biolabs nebuffer 2 1
    Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.
    Nebuffer 2 1, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/nebuffer 2 1/product/New England Biolabs
    Average 96 stars, based on 1 article reviews
    nebuffer 2 1 - by Bioz Stars, 2026-04
    96/100 stars
      Buy from Supplier

    98
    New England Biolabs nebuffer tm 2 1
    Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.
    Nebuffer Tm 2 1, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/nebuffer tm 2 1/product/New England Biolabs
    Average 98 stars, based on 1 article reviews
    nebuffer tm 2 1 - by Bioz Stars, 2026-04
    98/100 stars
      Buy from Supplier

    Image Search Results


    Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.

    Journal: Molecular Ecology Resources

    Article Title: Development and Laboratory Validation of a Field‐Deployable CRISPR ‐Cas12a eDNA Assay for Phylogeographic Lineage Detection in Arctic Char ( Salvelinus alpinus )

    doi: 10.1111/1755-0998.70125

    Figure Lengend Snippet: Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.

    Article Snippet: The effect of NEBuffer 2.1 concentration on LbCas12a assay performance was systematically evaluated using buffer concentrations ranging from 1× to 6× (Figure ).

    Techniques: Titration, Concentration Assay, CRISPR

    Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.

    Journal: Molecular Ecology Resources

    Article Title: Development and Laboratory Validation of a Field‐Deployable CRISPR ‐Cas12a eDNA Assay for Phylogeographic Lineage Detection in Arctic Char ( Salvelinus alpinus )

    doi: 10.1111/1755-0998.70125

    Figure Lengend Snippet: Influence of buffer concentrations on PAM site tolerance by LbCas12a. Titration of NEBuffer 2.1 indicated that a 5× concentration most effectively differentiated between lineages by modulating LbCas12a's tolerance for suboptimal PAM sites in Atlantic Subclade lineages 2–4, emphasizing the importance of buffer conditions in assay specificity. A total of 1 ng of tissue extracted DNA was used in each RPA‐CRISPR‐Cas reaction.

    Article Snippet: Buffer optimisation was similarly assessed by varying NEBuffer 2.1 concentrations, with the optimal condition defined as the one yielding the highest specificity without loss of sensitivity.

    Techniques: Titration, Concentration Assay, CRISPR