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    New England Biolabs sequencing adapters
    Sequencing Adapters, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 34027 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dna+sequences/T4+DNA+Ligase/10__3390_slash_arthropoda4040016-73-0-10
    Average 99 stars, based on 34027 article reviews
    sequencing adapters - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Generated:

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins.
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid (17) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B, coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid ( ) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B , coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Plasmid Preparation:

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins.
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid (17) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B, coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid ( ) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B , coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Mutagenesis:

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins.
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid (17) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B, coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid ( ) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B , coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Polymerase Chain Reaction:

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins.
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid (17) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B, coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid ( ) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B , coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Amplification:

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins.
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid (17) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B, coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid ( ) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B , coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Reverse Transcription:

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins.
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid (17) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B, coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid ( ) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B , coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Infection:

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins.
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid (17) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B, coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Article Title: Evolution of insect innate immunity through domestication of bacterial toxins
    Article Snippet: .. We generated untagged cdtB from the pET-His6-TEV-cdtB [2B-T] plasmid ( ) by standard mutagenesis. cdtB A (nt 61-840 of the cdtB aip56 A CDS), cdtB B (nt 61-840 of the cdtB aip56 B CDS), aip56 A (nt 841-1941 of the cdtB aip56 A CDS), and aip56 B (nt 841-1953 of the cdtB aip56 B CDS) were PCR amplified [using Q5 High-fidelity DNA polymerase (NEB)] from coding DNA sequences reverse transcribed from mRNA prepared from L. boulardi G486 infected wild-type D. ananassae larvae. .. To generate His6-tagged aip56-A and aip56-B or His6-TEV-tagged cdtB A and cdtB B , coding sequences were cloned into the pET-DUET1 (Merck-Millipore) or pDEST17 (Thermo Fisher Scientific) plasmids, respectively (without the predicted N-terminal signal peptides).

    Ligation:

    Article Title: Processing DNA Storage through Programmable Assembly in a Droplet-Based Fluidics System.
    Article Snippet: .. For ligation, the 5′ ends of DNA sequences were phosphorylated with T4 polynucleotide kinase (New England BioLabs, Inc.) The phosphorylated DNA sequences were hybridized with splint DNA in the annealing process, during which the temperature was decreased from 95 to 30 °C by 1 °C min−1 in a SimpliAmp thermal cycler (ThermoFisher Scientific, Inc., Waltham, MA, USA). .. All DNA droplets were prepared to achieve a final concentration of 4 μm in 50 mm NaCl buffer (Samchun Pure Chemical Co., Seoul, Korea).

    Article Title: Processing DNA Storage through Programmable Assembly in a Droplet‐Based Fluidics System
    Article Snippet: .. For ligation, the 5′ ends of DNA sequences were phosphorylated with T4 polynucleotide kinase (New England BioLabs, Inc.) The phosphorylated DNA sequences were hybridized with splint DNA in the annealing process, during which the temperature was decreased from 95 to 30 °C by 1 °C min −1 in a SimpliAmp thermal cycler (ThermoFisher Scientific, Inc., Waltham, MA, USA). .. All DNA droplets were prepared to achieve a final concentration of 4 μ m in 50 m m NaCl buffer (Samchun Pure Chemical Co., Seoul, Korea).

    Purification:

    Article Title: A Mutated Nme1Cas9 Is a Functional Alternative RNase to Both LwaCas13a and RfxCas13d in the Yeast S. cerevisiae .
    Article Snippet: .. Finally, the purified DNA sequences were ligated by T4 DNA ligase (NEB-M0202S) for 8 h at 16°C. ..

    Article Title: A Mutated Nme1Cas9 Is a Functional Alternative RNase to Both LwaCas13a and RfxCas13d in the Yeast S. cerevisiae
    Article Snippet: .. Finally, the purified DNA sequences were ligated by T4 DNA ligase (NEB-M0202S) for 8 h at 16°C. ..



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    Image Search Results


    (A) Architecture of the recombinase-based memory switch. The input module (pSwitch) contains IPTG- and arabinose-inducible promoters driving the expression of HbiF and FimE, respectively. The output module (pReporter) contains recombinase recognition sites flanking a constitutive promoter (Ptrc*) controlling RFP and GFP expression. Site-specific DNA inversion between the inverted repeats (IRL/IRR) reconfigures the recombination sites, reversing the promoter orientation and thereby toggling expression between RFP and GFP . (B) Flow cytometry analysis of cells initialized in the Green-On state and analyzed on day 3. The percentages of Red, uncommitted, and Green cells are reported as indicated. Red circles indicate the effect of recombinase leakiness and non-orthogonality. (C) Flow cytometry analysis of cells initialized in the Green-On state and switched to the Red-On state on day 3. (D) Flow cytometry analysis of cells initialized in the Red-On state and analyzed on day 3. (E) Flow cytometry analysis of cells initialized in the Red-On state and switched to the Green-On state on day 3.

    Journal: bioRxiv

    Article Title: Engineering Persistent and Rewritable Genetic Memory in Bacteria through Multiscale Plasmid Competition

    doi: 10.64898/2026.09.18.752696

    Figure Lengend Snippet: (A) Architecture of the recombinase-based memory switch. The input module (pSwitch) contains IPTG- and arabinose-inducible promoters driving the expression of HbiF and FimE, respectively. The output module (pReporter) contains recombinase recognition sites flanking a constitutive promoter (Ptrc*) controlling RFP and GFP expression. Site-specific DNA inversion between the inverted repeats (IRL/IRR) reconfigures the recombination sites, reversing the promoter orientation and thereby toggling expression between RFP and GFP . (B) Flow cytometry analysis of cells initialized in the Green-On state and analyzed on day 3. The percentages of Red, uncommitted, and Green cells are reported as indicated. Red circles indicate the effect of recombinase leakiness and non-orthogonality. (C) Flow cytometry analysis of cells initialized in the Green-On state and switched to the Red-On state on day 3. (D) Flow cytometry analysis of cells initialized in the Red-On state and analyzed on day 3. (E) Flow cytometry analysis of cells initialized in the Red-On state and switched to the Green-On state on day 3.

    Article Snippet: DNA sequencing used Plasmidsaurus DNA whole plasmid sequencing service.

    Techniques: Expressing, Flow Cytometry, Analysis