taq-polymerase Search Results


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  • 85
    Roche taq polymerase taq
    Taq Polymerase Taq, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    5 PRIME taq polymerase
    Taq Polymerase, supplied by 5 PRIME, used in various techniques. Bioz Stars score: 93/100, based on 332 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Avantor taq dna polymerase
    Taq Dna Polymerase, supplied by Avantor, used in various techniques. Bioz Stars score: 92/100, based on 141 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Bangalore Genei taq dna polymerase
    Sensitivity limits of multiplex RT-PCR. Lane 1 Amplification from tenfold diluted cDNA; lanes 2–6 amplicons from 10 −2 to 10 −6 fold diluted cDNA. Lanes 1–6 amplicons obtained with multiplexing kit; lanes 7–12 amplification with hot-start <t>Taq</t> <t>DNA</t> polymerase at same dilutions; lane M 100 bp marker
    Taq Dna Polymerase, supplied by Bangalore Genei, used in various techniques. Bioz Stars score: 94/100, based on 1139 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Bio Basic Canada taq polymerase
    Sensitivity limits of multiplex RT-PCR. Lane 1 Amplification from tenfold diluted cDNA; lanes 2–6 amplicons from 10 −2 to 10 −6 fold diluted cDNA. Lanes 1–6 amplicons obtained with multiplexing kit; lanes 7–12 amplification with hot-start <t>Taq</t> <t>DNA</t> polymerase at same dilutions; lane M 100 bp marker
    Taq Polymerase, supplied by Bio Basic Canada, used in various techniques. Bioz Stars score: 92/100, based on 135 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Bio-Rad taq polymerase
    BCG-induced increased NF-kappaB activity in J82 human cancer cell line . Human urothelial cancer cell line (J82) was exposed to BCG or saline for 24 hours and the cells were frozen and prepared for <t>ChiP-Q-PCR</t> assays. In this experiment the chromatin was precipitated with a p65 antibody. The final ChIP DNAs were then used as templates for Q-PCR reactions using primer pairs specific for each genomic region of interest. Q-PCR was carried out using <t>Taq</t> polymerase (iQ SYBR Green Supermix, Bio-Rad). Details of the primer sequences and the Genebank accession numbers are given in Table S4 (Additional File 4 ). Results are presented as
    Taq Polymerase, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 690 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    Bio-Serv taq polymerase
    BCG-induced increased NF-kappaB activity in J82 human cancer cell line . Human urothelial cancer cell line (J82) was exposed to BCG or saline for 24 hours and the cells were frozen and prepared for <t>ChiP-Q-PCR</t> assays. In this experiment the chromatin was precipitated with a p65 antibody. The final ChIP DNAs were then used as templates for Q-PCR reactions using primer pairs specific for each genomic region of interest. Q-PCR was carried out using <t>Taq</t> polymerase (iQ SYBR Green Supermix, Bio-Rad). Details of the primer sequences and the Genebank accession numbers are given in Table S4 (Additional File 4 ). Results are presented as
    Taq Polymerase, supplied by Bio-Serv, used in various techniques. Bioz Stars score: 90/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Bioneer Corporation taq polymerase
    BCG-induced increased NF-kappaB activity in J82 human cancer cell line . Human urothelial cancer cell line (J82) was exposed to BCG or saline for 24 hours and the cells were frozen and prepared for <t>ChiP-Q-PCR</t> assays. In this experiment the chromatin was precipitated with a p65 antibody. The final ChIP DNAs were then used as templates for Q-PCR reactions using primer pairs specific for each genomic region of interest. Q-PCR was carried out using <t>Taq</t> polymerase (iQ SYBR Green Supermix, Bio-Rad). Details of the primer sequences and the Genebank accession numbers are given in Table S4 (Additional File 4 ). Results are presented as
    Taq Polymerase, supplied by Bioneer Corporation, used in various techniques. Bioz Stars score: 92/100, based on 204 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    BioShop taq polymerase
    BCG-induced increased NF-kappaB activity in J82 human cancer cell line . Human urothelial cancer cell line (J82) was exposed to BCG or saline for 24 hours and the cells were frozen and prepared for <t>ChiP-Q-PCR</t> assays. In this experiment the chromatin was precipitated with a p65 antibody. The final ChIP DNAs were then used as templates for Q-PCR reactions using primer pairs specific for each genomic region of interest. Q-PCR was carried out using <t>Taq</t> polymerase (iQ SYBR Green Supermix, Bio-Rad). Details of the primer sequences and the Genebank accession numbers are given in Table S4 (Additional File 4 ). Results are presented as
    Taq Polymerase, supplied by BioShop, used in various techniques. Bioz Stars score: 92/100, based on 35 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Biotools B & M Labs taq polymerase
    BCG-induced increased NF-kappaB activity in J82 human cancer cell line . Human urothelial cancer cell line (J82) was exposed to BCG or saline for 24 hours and the cells were frozen and prepared for <t>ChiP-Q-PCR</t> assays. In this experiment the chromatin was precipitated with a p65 antibody. The final ChIP DNAs were then used as templates for Q-PCR reactions using primer pairs specific for each genomic region of interest. Q-PCR was carried out using <t>Taq</t> polymerase (iQ SYBR Green Supermix, Bio-Rad). Details of the primer sequences and the Genebank accession numbers are given in Table S4 (Additional File 4 ). Results are presented as
    Taq Polymerase, supplied by Biotools B & M Labs, used in various techniques. Bioz Stars score: 92/100, based on 62 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    Boehringer Mannheim taq polymerase
    ) (plasmid pSM2) with <t>Taq</t> polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with <t>Taq-Pwo</t> ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.
    Taq Polymerase, supplied by Boehringer Mannheim, used in various techniques. Bioz Stars score: 93/100, based on 1979 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    CinnaGen Co taq dna polymerase
    ) (plasmid pSM2) with <t>Taq</t> polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with <t>Taq-Pwo</t> ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.
    Taq Dna Polymerase, supplied by CinnaGen Co, used in various techniques. Bioz Stars score: 92/100, based on 1418 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Denville Scientific taq polymerase
    ) (plasmid pSM2) with <t>Taq</t> polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with <t>Taq-Pwo</t> ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.
    Taq Polymerase, supplied by Denville Scientific, used in various techniques. Bioz Stars score: 92/100, based on 207 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Epicentre Biotechnologies taq polymerase
    ) (plasmid pSM2) with <t>Taq</t> polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with <t>Taq-Pwo</t> ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.
    Taq Polymerase, supplied by Epicentre Biotechnologies, used in various techniques. Bioz Stars score: 92/100, based on 62 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Eppendorf AG taq polymerase
    ) (plasmid pSM2) with <t>Taq</t> polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with <t>Taq-Pwo</t> ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.
    Taq Polymerase, supplied by Eppendorf AG, used in various techniques. Bioz Stars score: 92/100, based on 843 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Eurobio taq polymerase
    ) (plasmid pSM2) with <t>Taq</t> polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with <t>Taq-Pwo</t> ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.
    Taq Polymerase, supplied by Eurobio, used in various techniques. Bioz Stars score: 92/100, based on 340 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Evrogen taq dna polymerase
    ) (plasmid pSM2) with <t>Taq</t> polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with <t>Taq-Pwo</t> ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.
    Taq Dna Polymerase, supplied by Evrogen, used in various techniques. Bioz Stars score: 92/100, based on 82 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    Feldan taq polymerase
    ) (plasmid pSM2) with <t>Taq</t> polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with <t>Taq-Pwo</t> ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.
    Taq Polymerase, supplied by Feldan, used in various techniques. Bioz Stars score: 93/100, based on 114 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Fisher Scientific taq polymerase
    ) (plasmid pSM2) with <t>Taq</t> polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with <t>Taq-Pwo</t> ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.
    Taq Polymerase, supplied by Fisher Scientific, used in various techniques. Bioz Stars score: 92/100, based on 349 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    GE Healthcare taq dna polymerase
    Incorporation enhancement attributable to terminator and polymerase variations. Incorporation is represented on a logarithmic scale relative to ddCTP incorporation by Vent <t>DNA</t> polymerase. Values for ThermoSequenase incorporation of ddCTP are inferred from Tabor and Richardson (20). <t>Taq</t> DNA polymerase failed to incorporate detectable amounts of acyCTP and thus is not represented. ROX analog incorporation was only examined for Vent and Vent A488L DNA polymerases.
    Taq Dna Polymerase, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 94/100, based on 2041 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    HiMedia Laboratories taq polymerase
    Incorporation enhancement attributable to terminator and polymerase variations. Incorporation is represented on a logarithmic scale relative to ddCTP incorporation by Vent <t>DNA</t> polymerase. Values for ThermoSequenase incorporation of ddCTP are inferred from Tabor and Richardson (20). <t>Taq</t> DNA polymerase failed to incorporate detectable amounts of acyCTP and thus is not represented. ROX analog incorporation was only examined for Vent and Vent A488L DNA polymerases.
    Taq Polymerase, supplied by HiMedia Laboratories, used in various techniques. Bioz Stars score: 92/100, based on 48 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Innogenetics taq polymerase
    Incorporation enhancement attributable to terminator and polymerase variations. Incorporation is represented on a logarithmic scale relative to ddCTP incorporation by Vent <t>DNA</t> polymerase. Values for ThermoSequenase incorporation of ddCTP are inferred from Tabor and Richardson (20). <t>Taq</t> DNA polymerase failed to incorporate detectable amounts of acyCTP and thus is not represented. ROX analog incorporation was only examined for Vent and Vent A488L DNA polymerases.
    Taq Polymerase, supplied by Innogenetics, used in various techniques. Bioz Stars score: 92/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    iNtRON Biotechnology taq polymerase
    Incorporation enhancement attributable to terminator and polymerase variations. Incorporation is represented on a logarithmic scale relative to ddCTP incorporation by Vent <t>DNA</t> polymerase. Values for ThermoSequenase incorporation of ddCTP are inferred from Tabor and Richardson (20). <t>Taq</t> DNA polymerase failed to incorporate detectable amounts of acyCTP and thus is not represented. ROX analog incorporation was only examined for Vent and Vent A488L DNA polymerases.
    Taq Polymerase, supplied by iNtRON Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 413 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Invitek Gmbh taq polymerase
    Incorporation enhancement attributable to terminator and polymerase variations. Incorporation is represented on a logarithmic scale relative to ddCTP incorporation by Vent <t>DNA</t> polymerase. Values for ThermoSequenase incorporation of ddCTP are inferred from Tabor and Richardson (20). <t>Taq</t> DNA polymerase failed to incorporate detectable amounts of acyCTP and thus is not represented. ROX analog incorporation was only examined for Vent and Vent A488L DNA polymerases.
    Taq Polymerase, supplied by Invitek Gmbh, used in various techniques. Bioz Stars score: 92/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Kaneka Corp taq polymerase
    Incorporation enhancement attributable to terminator and polymerase variations. Incorporation is represented on a logarithmic scale relative to ddCTP incorporation by Vent <t>DNA</t> polymerase. Values for ThermoSequenase incorporation of ddCTP are inferred from Tabor and Richardson (20). <t>Taq</t> DNA polymerase failed to incorporate detectable amounts of acyCTP and thus is not represented. ROX analog incorporation was only examined for Vent and Vent A488L DNA polymerases.
    Taq Polymerase, supplied by Kaneka Corp, used in various techniques. Bioz Stars score: 92/100, based on 207 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Sensitivity limits of multiplex RT-PCR. Lane 1 Amplification from tenfold diluted cDNA; lanes 2–6 amplicons from 10 −2 to 10 −6 fold diluted cDNA. Lanes 1–6 amplicons obtained with multiplexing kit; lanes 7–12 amplification with hot-start Taq DNA polymerase at same dilutions; lane M 100 bp marker

    Journal: Indian Journal of Microbiology

    Article Title: Simultaneous Detection of Major Pome Fruit Viruses and a Viroid

    doi: 10.1007/s12088-013-0431-y

    Figure Lengend Snippet: Sensitivity limits of multiplex RT-PCR. Lane 1 Amplification from tenfold diluted cDNA; lanes 2–6 amplicons from 10 −2 to 10 −6 fold diluted cDNA. Lanes 1–6 amplicons obtained with multiplexing kit; lanes 7–12 amplification with hot-start Taq DNA polymerase at same dilutions; lane M 100 bp marker

    Article Snippet: For RT, all conditions were the same except random hexamer primers 100 ng were used for cDNA synthesis and for multiplex PCR reaction 5 μl cDNA, 0.16 pmol of each primers pair, 1.2× Taq buffer, 0.3 mM dNTPs, 1.5 units of Taq DNA polymerase (Bangalore Genei) and 1.5 mM MgCl2 (additional) in final concentration was used. cDNA was amplified for 35 cycles (40 s at 94 °C, 75 s at 58 °C, and 90 s at 72 °C).

    Techniques: Multiplex Assay, Reverse Transcription Polymerase Chain Reaction, Amplification, Multiplexing, Marker

    BCG-induced increased NF-kappaB activity in J82 human cancer cell line . Human urothelial cancer cell line (J82) was exposed to BCG or saline for 24 hours and the cells were frozen and prepared for ChiP-Q-PCR assays. In this experiment the chromatin was precipitated with a p65 antibody. The final ChIP DNAs were then used as templates for Q-PCR reactions using primer pairs specific for each genomic region of interest. Q-PCR was carried out using Taq polymerase (iQ SYBR Green Supermix, Bio-Rad). Details of the primer sequences and the Genebank accession numbers are given in Table S4 (Additional File 4 ). Results are presented as

    Journal: BMC Immunology

    Article Title: Molecular networks discriminating mouse bladder responses to intravesical bacillus Calmette-Guerin (BCG), LPS, and TNF-?

    doi: 10.1186/1471-2172-9-4

    Figure Lengend Snippet: BCG-induced increased NF-kappaB activity in J82 human cancer cell line . Human urothelial cancer cell line (J82) was exposed to BCG or saline for 24 hours and the cells were frozen and prepared for ChiP-Q-PCR assays. In this experiment the chromatin was precipitated with a p65 antibody. The final ChIP DNAs were then used as templates for Q-PCR reactions using primer pairs specific for each genomic region of interest. Q-PCR was carried out using Taq polymerase (iQ SYBR Green Supermix, Bio-Rad). Details of the primer sequences and the Genebank accession numbers are given in Table S4 (Additional File 4 ). Results are presented as "transcription events detected per 1000 cells" for each gene tested. Error bars correspond to standard deviations from the triplicate Q-PCR reactions. Control represents an un-transcribed region of the genome. Asterisks indicate a statistical significant difference (p

    Article Snippet: Quantitative PCR was carried out using Taq polymerase (iQ SYBR Green Supermix, Bio-Rad).

    Techniques: Activity Assay, Chromatin Immunoprecipitation, Polymerase Chain Reaction, SYBR Green Assay

    ) (plasmid pSM2) with Taq polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with Taq-Pwo ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.

    Journal: Journal of Clinical Microbiology

    Article Title: Amplification of Full-Length Hepatitis B Virus Genomes from Samples from Patients with Low Levels of Viremia: Frequency and Functional Consequences of PCR-Introduced Mutations

    doi:

    Figure Lengend Snippet: ) (plasmid pSM2) with Taq polymerase. (B) Analysis of cloned genomes amplified from 90 template molecules of wild-type HBV DNA with Taq-Pwo ) (plasmid pHBV-SapI); ⊘, mock transfection; M, marker lane with 3.2-kb double-stranded (ds) and single-stranded (ss) HBV DNA. Note that the bands at the 3.2-kb position seen in all lanes of the amplified genomes represent input rather than progeny HBV DNA.

    Article Snippet: Therefore, we calculated the error rate of Taq polymerase and Taq-Pwo polymerase mixture in the 40-cycle full-length PCR.

    Techniques: Plasmid Preparation, Clone Assay, Amplification, Transfection, Marker

    Incorporation enhancement attributable to terminator and polymerase variations. Incorporation is represented on a logarithmic scale relative to ddCTP incorporation by Vent DNA polymerase. Values for ThermoSequenase incorporation of ddCTP are inferred from Tabor and Richardson (20). Taq DNA polymerase failed to incorporate detectable amounts of acyCTP and thus is not represented. ROX analog incorporation was only examined for Vent and Vent A488L DNA polymerases.

    Journal: Nucleic Acids Research

    Article Title: Acyclic and dideoxy terminator preferences denote divergent sugar recognition by archaeon and Taq DNA polymerases

    doi:

    Figure Lengend Snippet: Incorporation enhancement attributable to terminator and polymerase variations. Incorporation is represented on a logarithmic scale relative to ddCTP incorporation by Vent DNA polymerase. Values for ThermoSequenase incorporation of ddCTP are inferred from Tabor and Richardson (20). Taq DNA polymerase failed to incorporate detectable amounts of acyCTP and thus is not represented. ROX analog incorporation was only examined for Vent and Vent A488L DNA polymerases.

    Article Snippet: Taq DNA polymerase (Amersham Pharmacia Biotech, Piscataway, NJ) and its F667Y derivative Thermo Sequenase (Amersham Pharmacia Biotech) naturally lack this activity, while the archaeon DNA polymerases have been genetically modified within the conserved exonuclease motif DIE to AIA to eliminate this activity ( – ).

    Techniques:

    Incorporation of ddCTP and acyCTP. Titration assay for the indicated terminators using ( A ) Taq ( B ) Vent, ( C ) ThermoSequenase or ( D ) Vent A488L DNA polymerase. Extension of a 32 P-labeled primer on a M13mp18 single-stranded substrate was examined in the presence of the indicated ratios of terminator to dNTP. The lane marked dNTP is a control reaction performed in the absence of terminators.

    Journal: Nucleic Acids Research

    Article Title: Acyclic and dideoxy terminator preferences denote divergent sugar recognition by archaeon and Taq DNA polymerases

    doi:

    Figure Lengend Snippet: Incorporation of ddCTP and acyCTP. Titration assay for the indicated terminators using ( A ) Taq ( B ) Vent, ( C ) ThermoSequenase or ( D ) Vent A488L DNA polymerase. Extension of a 32 P-labeled primer on a M13mp18 single-stranded substrate was examined in the presence of the indicated ratios of terminator to dNTP. The lane marked dNTP is a control reaction performed in the absence of terminators.

    Article Snippet: Taq DNA polymerase (Amersham Pharmacia Biotech, Piscataway, NJ) and its F667Y derivative Thermo Sequenase (Amersham Pharmacia Biotech) naturally lack this activity, while the archaeon DNA polymerases have been genetically modified within the conserved exonuclease motif DIE to AIA to eliminate this activity ( – ).

    Techniques: Titration, Labeling