lambda exonuclease iii  (Thermo Fisher)


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    Name:
    Lambda Exonuclease 10 U µL
    Description:
    Thermo Scientific Lambda Exonuclease is a highly processive 5 →3 exodeoxyribonuclease It selectively digests the 5 phosphorylated strand of double stranded DNA The enzyme exhibits low activity on single stranded DNA and non phosphorylated DNA and has no activity at nicks and limited activity at gaps in DNA Highlights• Active in Thermo Scientific PCR buffersApplications• Generating single stranded PCR products for use in • DNA sequencing• Analysis of DNA single strand conformation polymorphism SSCP • Rolling circle amplification• Producing single stranded DNA from double stranded DNA fragments• Cloning of PCR productsNoteUse of this enzyme in certain applications may be covered by patents and may require a license
    Catalog Number:
    en0561
    Price:
    None
    Applications:
    Cloning|PCR Cloning
    Category:
    Proteins Enzymes Peptides
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    Structured Review

    Thermo Fisher lambda exonuclease iii
    Thermo Scientific Lambda Exonuclease is a highly processive 5 →3 exodeoxyribonuclease It selectively digests the 5 phosphorylated strand of double stranded DNA The enzyme exhibits low activity on single stranded DNA and non phosphorylated DNA and has no activity at nicks and limited activity at gaps in DNA Highlights• Active in Thermo Scientific PCR buffersApplications• Generating single stranded PCR products for use in • DNA sequencing• Analysis of DNA single strand conformation polymorphism SSCP • Rolling circle amplification• Producing single stranded DNA from double stranded DNA fragments• Cloning of PCR productsNoteUse of this enzyme in certain applications may be covered by patents and may require a license
    https://www.bioz.com/result/lambda exonuclease iii/product/Thermo Fisher
    Average 99 stars, based on 4 article reviews
    Price from $9.99 to $1999.99
    lambda exonuclease iii - by Bioz Stars, 2020-11
    99/100 stars

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    Related Articles

    Amplification:

    Article Title: Scalable and cost-effective ribonuclease-based rRNA depletion for transcriptomics
    Article Snippet: .. Amplicon products were purified using 1X SeraPure SPRI beads( , ) and then subjected to a lambda exonuclease [ThermoFisher EN0562] digestion, which selectively digests the 5’-phosphorylated strands resulting in amplicon ssDNA probes complementary to ribosomal RNAs. .. Finally, 16S amplicon probe and 23S amplicon probe were mixed in equimolar amounts to generate amplicon probe mixes used in this study.

    Synthesized:

    Article Title: Preferential Localization of Human Origins of DNA Replication at the 5?-Ends of Expressed Genes and at Evolutionarily Conserved DNA Sequences
    Article Snippet: .. After λ-exonuclease treatment of the DNA pool in the size range of 400–800 bp, we synthesized a double stranded DNA population required for massively parallel sequencing using the Klenow fragment of DNA polymerase I (Invitrogen, Carlsbed, CA) and random primers (Invitrogen, Carlsbad, CA). .. Random priming and DNA synthesis were performed according to the manufacturer's protocol except that the samples were incubated for an hour at 37°C.

    Purification:

    Article Title: Scalable and cost-effective ribonuclease-based rRNA depletion for transcriptomics
    Article Snippet: .. Amplicon products were purified using 1X SeraPure SPRI beads( , ) and then subjected to a lambda exonuclease [ThermoFisher EN0562] digestion, which selectively digests the 5’-phosphorylated strands resulting in amplicon ssDNA probes complementary to ribosomal RNAs. .. Finally, 16S amplicon probe and 23S amplicon probe were mixed in equimolar amounts to generate amplicon probe mixes used in this study.

    Incubation:

    Article Title: Stable Complexes Formed by HIV-1 Reverse Transcriptase at Distinct Positions on the Primer-Template Controlled by Binding Deoxynucleoside Triphosphates or Foscarnet
    Article Snippet: .. For upstream mapping of the borders of the stable complexes, 5 nM 3'-[32 P] ddAMP-terminated, 5'-phosphorylated L32 primer annealed to excess WL50 template was incubated with 200 nM HIV-1 RT and dNTP, foscarnet or no ligand as indicated in the figures, in 10 μl RB buffer for 15 min at 37°C, followed by incubation at 4°C for 5 min. After addition of 1.2 U lambda exonuclease (USB Corp.), the samples were incubated at 37°C for 8 min followed by heat-inactivation at 90°C for 5 min. For downstream mapping of the borders of the stable complexes, 5 nM 3'-[32 P]ddAMP-labeled WL65 template annealed to excess ddAMP-terminated L32 primer was incubated with 12.5 nM WT HIV-1 RT and ligand (0.8 mM dNTP, 3.2 mM foscarnet, or no ligand) in 10 μl RB buffer for 15 min at 37°C, followed by incubation at 4°C for 5 min. .. Ten units of RecJf (New England Biolabs) were added and the samples were incubated at 37°C for 10 min followed by heat-inactivation at 90°C for 5 min. For both upstream and downstream mapping, 12 μl loading buffer were added and the products were separated by electrophoresis through a denaturing 20% polyacrylamide gel.

    Sequencing:

    Article Title: X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisation
    Article Snippet: .. The Dp427m transcript was explored using nested RT-PCRs with nine pairs of primers designed to amplify overlapping segments of the cDNA, based on the published canine dystrophin cDNA sequence (ESNCAFT00000036277) as follows: exons 3 to 10, exons 10 to 20, exons 15 to 22, exons 21 to 26, exons 25 to 36, exons 35 to 46, exons 45 to 56, exons 55 to 67 and exons 66 to 79 (sequences in Table S1). .. For these RT-PCR experiments, the PCR MasterMix kit (Promega) was used.

    Article Title: Preferential Localization of Human Origins of DNA Replication at the 5?-Ends of Expressed Genes and at Evolutionarily Conserved DNA Sequences
    Article Snippet: .. After λ-exonuclease treatment of the DNA pool in the size range of 400–800 bp, we synthesized a double stranded DNA population required for massively parallel sequencing using the Klenow fragment of DNA polymerase I (Invitrogen, Carlsbed, CA) and random primers (Invitrogen, Carlsbad, CA). .. Random priming and DNA synthesis were performed according to the manufacturer's protocol except that the samples were incubated for an hour at 37°C.

    Binding Assay:

    Article Title: Direct binding to antigen-coated beads refines the specificity and cross-reactivity of four monoclonal antibodies that recognize polymorphic epitopes of HLA class I molecules
    Article Snippet: .. Gen-Probe beads showed a mean reduction in W6/32 binding of 54% (range 35–69%), 52% (range 20–71%) and 50% (range 23–75%) for HLA-A, -B and -C allotypes respectively as compared to One Lambda beads. ..

    Article Title: Direct binding to antigen-coated beads refines the specificity and cross-reactivity of four monoclonal antibodies that recognize polymorphic epitopes of HLA class I molecules
    Article Snippet: .. Comparably strong reactions for HLA-B*07:02, B*42:01 and B*81:01 were observed with the One Lambda beads, but the binding of BB7.1 to the Gen-Probe B*42:01 bead was relatively weak. .. Even weaker was the binding to the B*07:03 bead, which may reflect an inherent difference between B*07:02 and B*07:03 in their avidities for BB7.1.

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  • 99
    Thermo Fisher lambda exonuclease iii
    Lambda Exonuclease Iii, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lambda exonuclease iii/product/Thermo Fisher
    Average 99 stars, based on 4 article reviews
    Price from $9.99 to $1999.99
    lambda exonuclease iii - by Bioz Stars, 2020-11
    99/100 stars
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