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    Kapa Biosystems kapa hifi hot start dna polymerase
    Kapa Hifi Hot Start Dna Polymerase, supplied by Kapa Biosystems, used in various techniques. Bioz Stars score: 91/100, based on 43 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kapa hifi hot start dna polymerase/product/Kapa Biosystems
    Average 91 stars, based on 43 article reviews
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    kapa hifi hot start dna polymerase - by Bioz Stars, 2020-08
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    91
    Roche kapa hifi hot start dna polymerase
    Polymorphisms detected in the ITS-1 sequence of paper mulberry barkcloth textiles. Multiple alignment of 20 selected partial ITS sequences (50 bp) of textile samples. Image adapted from Bioedit 7.1.3.0. The reverse sequence (with primer ITS-C) is shown. The red arrow indicates the polymorphic nucleotide at the relative position 203 [ 21 ]. HM623778 corresponds to the ID of the B . papyrifera ITS region published in Genbank. M = double signal A/C at this position. Y = C or T; S = C or G; W = A or T. Bite Score (BS), Query Coverage (QC), E-values and identity percentage (Id) are indicated on the right. Extension names OT = sample amplified at the University of Otago using <t>KAPA</t> <t>HiFi</t> Hot Start <t>DNA</t> Polymerase; BM = sample amplified using GoTaq® G2 DNA Polymerase at the Faculty of Chemical and Pharmaceutical Sciences, University of Chile; MD = sample amplified using GoTaq® G2 Hot Start Flexi DNA Polymerase at the Faculty of Medicine, University of Chile, and P = sample amplified after extract purification.
    Kapa Hifi Hot Start Dna Polymerase, supplied by Roche, used in various techniques. Bioz Stars score: 91/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kapa hifi hot start dna polymerase/product/Roche
    Average 91 stars, based on 2 article reviews
    Price from $9.99 to $1999.99
    kapa hifi hot start dna polymerase - by Bioz Stars, 2020-08
    91/100 stars
      Buy from Supplier

    90
    Kapa Biosystems kapa hifi hot start ready mix
    Polymorphisms detected in the ITS-1 sequence of paper mulberry barkcloth textiles. Multiple alignment of 20 selected partial ITS sequences (50 bp) of textile samples. Image adapted from Bioedit 7.1.3.0. The reverse sequence (with primer ITS-C) is shown. The red arrow indicates the polymorphic nucleotide at the relative position 203 [ 21 ]. HM623778 corresponds to the ID of the B . papyrifera ITS region published in Genbank. M = double signal A/C at this position. Y = C or T; S = C or G; W = A or T. Bite Score (BS), Query Coverage (QC), E-values and identity percentage (Id) are indicated on the right. Extension names OT = sample amplified at the University of Otago using <t>KAPA</t> <t>HiFi</t> Hot Start <t>DNA</t> Polymerase; BM = sample amplified using GoTaq® G2 DNA Polymerase at the Faculty of Chemical and Pharmaceutical Sciences, University of Chile; MD = sample amplified using GoTaq® G2 Hot Start Flexi DNA Polymerase at the Faculty of Medicine, University of Chile, and P = sample amplified after extract purification.
    Kapa Hifi Hot Start Ready Mix, supplied by Kapa Biosystems, used in various techniques. Bioz Stars score: 90/100, based on 167 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kapa hifi hot start ready mix/product/Kapa Biosystems
    Average 90 stars, based on 167 article reviews
    Price from $9.99 to $1999.99
    kapa hifi hot start ready mix - by Bioz Stars, 2020-08
    90/100 stars
      Buy from Supplier

    Image Search Results


    Polymorphisms detected in the ITS-1 sequence of paper mulberry barkcloth textiles. Multiple alignment of 20 selected partial ITS sequences (50 bp) of textile samples. Image adapted from Bioedit 7.1.3.0. The reverse sequence (with primer ITS-C) is shown. The red arrow indicates the polymorphic nucleotide at the relative position 203 [ 21 ]. HM623778 corresponds to the ID of the B . papyrifera ITS region published in Genbank. M = double signal A/C at this position. Y = C or T; S = C or G; W = A or T. Bite Score (BS), Query Coverage (QC), E-values and identity percentage (Id) are indicated on the right. Extension names OT = sample amplified at the University of Otago using KAPA HiFi Hot Start DNA Polymerase; BM = sample amplified using GoTaq® G2 DNA Polymerase at the Faculty of Chemical and Pharmaceutical Sciences, University of Chile; MD = sample amplified using GoTaq® G2 Hot Start Flexi DNA Polymerase at the Faculty of Medicine, University of Chile, and P = sample amplified after extract purification.

    Journal: PLoS ONE

    Article Title: A tale of textiles: Genetic characterization of historical paper mulberry barkcloth from Oceania

    doi: 10.1371/journal.pone.0233113

    Figure Lengend Snippet: Polymorphisms detected in the ITS-1 sequence of paper mulberry barkcloth textiles. Multiple alignment of 20 selected partial ITS sequences (50 bp) of textile samples. Image adapted from Bioedit 7.1.3.0. The reverse sequence (with primer ITS-C) is shown. The red arrow indicates the polymorphic nucleotide at the relative position 203 [ 21 ]. HM623778 corresponds to the ID of the B . papyrifera ITS region published in Genbank. M = double signal A/C at this position. Y = C or T; S = C or G; W = A or T. Bite Score (BS), Query Coverage (QC), E-values and identity percentage (Id) are indicated on the right. Extension names OT = sample amplified at the University of Otago using KAPA HiFi Hot Start DNA Polymerase; BM = sample amplified using GoTaq® G2 DNA Polymerase at the Faculty of Chemical and Pharmaceutical Sciences, University of Chile; MD = sample amplified using GoTaq® G2 Hot Start Flexi DNA Polymerase at the Faculty of Medicine, University of Chile, and P = sample amplified after extract purification.

    Article Snippet: Analyses at the University of Otago were performed with KAPA HiFi Hot Start DNA Polymerase (Kapa Biosystems, Wilmington, MS, USA), while GoTaq® G2 Flexi DNA Polymerase and GoTaq® G2 Hot Start Polymerase (Promega, Madison, WI, USA) were used at the facilities in Chile.

    Techniques: Sequencing, Amplification, Purification