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nebnext multiplex oligos for illum  (New England Biolabs)


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    Structured Review

    New England Biolabs nebnext multiplex oligos for illum

    Nebnext Multiplex Oligos For Illum, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 2193 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nebnext+multiplex+oligos/NEBNext+Multiplex+Oligos+for+Illumina/pmc13651819-162-0-0
    Average 96 stars, based on 2193 article reviews
    nebnext multiplex oligos for illum - by Bioz Stars, 2026-10
    96/100 stars

    Images

    1) Product Images from "Gapmers targeting conserved SARS-CoV-2 single-stranded regions reduce viral load and reshape inflammatory macrophage responses"

    Article Title: Gapmers targeting conserved SARS-CoV-2 single-stranded regions reduce viral load and reshape inflammatory macrophage responses

    Journal: iScience

    doi: 10.1016/j.isci.2026.117639


    Figure Legend Snippet:

    Techniques Used: Virus, Variant Assay, Recombinant, Reverse Transcription, Diagnostic Assay, Luminex, Ligation, Multiplex Assay, Generated, Software

    Related Articles

    Purification:

    Article Title: DNA-PKcs inhibitor AZD7648 reveals sgRNA cross-contaminants and enhanced sensitivity of genome engineering off-target activity in HSPCs.
    Article Snippet: .. The purified PCR amplicons were hen end repaired, A-tailed, ligated to an adapter, and purified ollowing the protocol in NEBNext ® UltraTM II DNA Library rep Kit for Illumina ® and NEBNext ® Multiplex Oligos for llumina ®. gRNA sequencing omplementary DNA (cDNA) of the sgRNAs were syntheized by mixing 200 ng sgRNA with 2 mM dNTP mix (Thermo Fisher), and 1 μM sgRNA scaffold specific primer (Merck) and incubated at 70 ◦C for 5 min. A reverse transcription mixture consisting of 1 × Template-Switching RT Buffer (NEB), Template-Switching RT Enzyme Mix (NEB), and 3.75 μM adapter-linked template-switching oligo (TSO) was then immediately added to the primer annealing mixture and incubated at 42 ◦C for 90 min and 85 ◦C for 5 min. sgRNA cDNA was diluted 1:10 and subjected to a nested PCR using 0.2 μM adapter-linked primer upstream of the original RT scaffold specific primer and Q5 Hot-start HF 2 × master mix (NEB). .. Amplicons were then purified using AMPure XP Bead-Based Reagent (BECKMAN COULTER) and barcoded following the 7 cycle PCR with NEBNext ® Multiplex Oligos for Illumina ®.

    Polymerase Chain Reaction:

    Article Title: DNA-PKcs inhibitor AZD7648 reveals sgRNA cross-contaminants and enhanced sensitivity of genome engineering off-target activity in HSPCs.
    Article Snippet: .. The purified PCR amplicons were hen end repaired, A-tailed, ligated to an adapter, and purified ollowing the protocol in NEBNext ® UltraTM II DNA Library rep Kit for Illumina ® and NEBNext ® Multiplex Oligos for llumina ®. gRNA sequencing omplementary DNA (cDNA) of the sgRNAs were syntheized by mixing 200 ng sgRNA with 2 mM dNTP mix (Thermo Fisher), and 1 μM sgRNA scaffold specific primer (Merck) and incubated at 70 ◦C for 5 min. A reverse transcription mixture consisting of 1 × Template-Switching RT Buffer (NEB), Template-Switching RT Enzyme Mix (NEB), and 3.75 μM adapter-linked template-switching oligo (TSO) was then immediately added to the primer annealing mixture and incubated at 42 ◦C for 90 min and 85 ◦C for 5 min. sgRNA cDNA was diluted 1:10 and subjected to a nested PCR using 0.2 μM adapter-linked primer upstream of the original RT scaffold specific primer and Q5 Hot-start HF 2 × master mix (NEB). .. Amplicons were then purified using AMPure XP Bead-Based Reagent (BECKMAN COULTER) and barcoded following the 7 cycle PCR with NEBNext ® Multiplex Oligos for Illumina ®.

    Article Title: HM-DyadCap - capture and mapping of 5-hydroxymethylcytosine/5-methylcytosine CpG dyads in mammalian DNA.
    Article Snippet: .. Preparation of Illumina libraries and NGS sequencing Enriched DNA fragments were PCR amplified using the NEBNext Ultra II DNA Library Prep Kit for Illumina (NEB, version 6.1_5/20) using NEBNext Multiplex Oligos (NEB, E73359). ..

    Article Title: HM-DyadCap – capture and mapping of 5-hydroxymethylcytosine/5-methylcytosine CpG dyads in mammalian DNA
    Article Snippet: .. Enriched DNA fragments were PCR amplified using the NEBNext Ultra II DNA Library Prep Kit for Illumina (NEB, version 6.1_5/20) using NEBNext Multiplex Oligos (NEB, E73359). ..

    Multiplex Assay:

    Article Title: DNA-PKcs inhibitor AZD7648 reveals sgRNA cross-contaminants and enhanced sensitivity of genome engineering off-target activity in HSPCs.
    Article Snippet: .. The purified PCR amplicons were hen end repaired, A-tailed, ligated to an adapter, and purified ollowing the protocol in NEBNext ® UltraTM II DNA Library rep Kit for Illumina ® and NEBNext ® Multiplex Oligos for llumina ®. gRNA sequencing omplementary DNA (cDNA) of the sgRNAs were syntheized by mixing 200 ng sgRNA with 2 mM dNTP mix (Thermo Fisher), and 1 μM sgRNA scaffold specific primer (Merck) and incubated at 70 ◦C for 5 min. A reverse transcription mixture consisting of 1 × Template-Switching RT Buffer (NEB), Template-Switching RT Enzyme Mix (NEB), and 3.75 μM adapter-linked template-switching oligo (TSO) was then immediately added to the primer annealing mixture and incubated at 42 ◦C for 90 min and 85 ◦C for 5 min. sgRNA cDNA was diluted 1:10 and subjected to a nested PCR using 0.2 μM adapter-linked primer upstream of the original RT scaffold specific primer and Q5 Hot-start HF 2 × master mix (NEB). .. Amplicons were then purified using AMPure XP Bead-Based Reagent (BECKMAN COULTER) and barcoded following the 7 cycle PCR with NEBNext ® Multiplex Oligos for Illumina ®.

    Article Title: Molding the Rice Methylome for Disease Resistance
    Article Snippet: High-purity genomic DNA was extracted using IllustraTM NucleonTM PhytoPureTM kit (Cytiva), then sheared to ∼500bp fragments through sonication using Covaris M220. .. Enzymatic conversion of methylated cytosines and library preparation were performed using NEBNext® Enzymatic Methyl-seq Kit and NEBNext® Multiplex Oligos for Enzymatic Methyl-seq (New England Biolabs) according to the provided instructions, using sodium hydroxide for DNA denaturation and performing libraries size selection (470-520bp) for enrichment of larger inserts. .. Libraries were sequenced on Illumina NovaSeq X Plus using 2x 150bp paired-end configuration.

    Article Title: Alu-mediated RNA duplexes are associated with widespread exon skipping across primate transcriptomes
    Article Snippet: .. Reverse transcription was performed with SuperScript IV at 50 °C for 1 h using 1 μM 3′ adaptor–specific primer (5’ -TTCAGACGTGTGCTCTTCCGATCTATTGATGGTGCCTACAG-3’) and 1 μM template-switch oligo (TSO) containing a 10-nt unique molecular identifier (UMI) (5’ -CTT TCC CTA CAC GAC GCT CTT CCG ATCT NNNNNNNNNN TAC rGrGrG/3phos/−3’). cDNA fragments of 150–300nt were size-selected on a 6% urea-PAGE gel, then amplified with NEBNext Multiplex Oligos using Q5 DNA polymerase (NEB) for 12 cycles. .. cDNA fragments of 150–300nt were size-selected on a 6% urea-PAGE gel, then amplified with NEBNext Multiplex Oligos using Q5 DNA polymerase (NEB) for 12 cycles.

    Article Title: Epigenetic control of S100A8/A9-driven monocytic inflammation licenses anti-leukemic functionality of immature NK cells during hematopoietic stem cell differentiation
    Article Snippet: .. Libraries were generated from total RNA after poly(A)^+^ mRNA enrichment using the NEBNext Ultra II Directional RNA Library Prep Kit with NEBNext Multiplex Oligos (NEB) according to the manufacturer’s instructions. .. Sequencing was performed on an Illumina NovaSeq 6000 using 150 bp paired-end reads.

    Article Title: Cancer detection and classification using methylome analysis
    Article Snippet: Briefly, for MeDIP, the Diagenode MagMeDIP kit (Cat #C02010021) was used following the manufacturer's protocol with some modifications. .. The optimal number of cycles to amplify each library was determined through the use of qPCR, after which the samples were amplified using the KAPA HiFi Hotstart Mastermix and the NEBNext multiplex oligos added to a final concentration of 0.3 μM. ..

    Article Title: deluxpore: a Nextflow pipeline for demultiplexing Illumina dual-indexed Nanopore libraries
    Article Snippet: .. As a solution, target enrichment can be performed on Illumina-indexed libraries, whereby dual indexes incorporated during library preparation allow samples to be pooled prior to capture hybridisation, after which the enriched pool is converted into a Nanopore-compatible library for MinION sequencing; a strategy recently applied to microbial gene capture using NEBNext Multiplex Oligos ( ). .. Importantly, this hybrid approach lacks practical implementation: standard Illumina demultiplexers cannot process Nanopore-derived data.

    Article Title: HM-DyadCap - capture and mapping of 5-hydroxymethylcytosine/5-methylcytosine CpG dyads in mammalian DNA.
    Article Snippet: .. Preparation of Illumina libraries and NGS sequencing Enriched DNA fragments were PCR amplified using the NEBNext Ultra II DNA Library Prep Kit for Illumina (NEB, version 6.1_5/20) using NEBNext Multiplex Oligos (NEB, E73359). ..

    Article Title: HM-DyadCap – capture and mapping of 5-hydroxymethylcytosine/5-methylcytosine CpG dyads in mammalian DNA
    Article Snippet: .. Enriched DNA fragments were PCR amplified using the NEBNext Ultra II DNA Library Prep Kit for Illumina (NEB, version 6.1_5/20) using NEBNext Multiplex Oligos (NEB, E73359). ..

    Sequencing:

    Article Title: DNA-PKcs inhibitor AZD7648 reveals sgRNA cross-contaminants and enhanced sensitivity of genome engineering off-target activity in HSPCs.
    Article Snippet: .. The purified PCR amplicons were hen end repaired, A-tailed, ligated to an adapter, and purified ollowing the protocol in NEBNext ® UltraTM II DNA Library rep Kit for Illumina ® and NEBNext ® Multiplex Oligos for llumina ®. gRNA sequencing omplementary DNA (cDNA) of the sgRNAs were syntheized by mixing 200 ng sgRNA with 2 mM dNTP mix (Thermo Fisher), and 1 μM sgRNA scaffold specific primer (Merck) and incubated at 70 ◦C for 5 min. A reverse transcription mixture consisting of 1 × Template-Switching RT Buffer (NEB), Template-Switching RT Enzyme Mix (NEB), and 3.75 μM adapter-linked template-switching oligo (TSO) was then immediately added to the primer annealing mixture and incubated at 42 ◦C for 90 min and 85 ◦C for 5 min. sgRNA cDNA was diluted 1:10 and subjected to a nested PCR using 0.2 μM adapter-linked primer upstream of the original RT scaffold specific primer and Q5 Hot-start HF 2 × master mix (NEB). .. Amplicons were then purified using AMPure XP Bead-Based Reagent (BECKMAN COULTER) and barcoded following the 7 cycle PCR with NEBNext ® Multiplex Oligos for Illumina ®.

    Article Title: deluxpore: a Nextflow pipeline for demultiplexing Illumina dual-indexed Nanopore libraries
    Article Snippet: .. As a solution, target enrichment can be performed on Illumina-indexed libraries, whereby dual indexes incorporated during library preparation allow samples to be pooled prior to capture hybridisation, after which the enriched pool is converted into a Nanopore-compatible library for MinION sequencing; a strategy recently applied to microbial gene capture using NEBNext Multiplex Oligos ( ). .. Importantly, this hybrid approach lacks practical implementation: standard Illumina demultiplexers cannot process Nanopore-derived data.

    Article Title: HM-DyadCap - capture and mapping of 5-hydroxymethylcytosine/5-methylcytosine CpG dyads in mammalian DNA.
    Article Snippet: .. Preparation of Illumina libraries and NGS sequencing Enriched DNA fragments were PCR amplified using the NEBNext Ultra II DNA Library Prep Kit for Illumina (NEB, version 6.1_5/20) using NEBNext Multiplex Oligos (NEB, E73359). ..

    Incubation:

    Article Title: DNA-PKcs inhibitor AZD7648 reveals sgRNA cross-contaminants and enhanced sensitivity of genome engineering off-target activity in HSPCs.
    Article Snippet: .. The purified PCR amplicons were hen end repaired, A-tailed, ligated to an adapter, and purified ollowing the protocol in NEBNext ® UltraTM II DNA Library rep Kit for Illumina ® and NEBNext ® Multiplex Oligos for llumina ®. gRNA sequencing omplementary DNA (cDNA) of the sgRNAs were syntheized by mixing 200 ng sgRNA with 2 mM dNTP mix (Thermo Fisher), and 1 μM sgRNA scaffold specific primer (Merck) and incubated at 70 ◦C for 5 min. A reverse transcription mixture consisting of 1 × Template-Switching RT Buffer (NEB), Template-Switching RT Enzyme Mix (NEB), and 3.75 μM adapter-linked template-switching oligo (TSO) was then immediately added to the primer annealing mixture and incubated at 42 ◦C for 90 min and 85 ◦C for 5 min. sgRNA cDNA was diluted 1:10 and subjected to a nested PCR using 0.2 μM adapter-linked primer upstream of the original RT scaffold specific primer and Q5 Hot-start HF 2 × master mix (NEB). .. Amplicons were then purified using AMPure XP Bead-Based Reagent (BECKMAN COULTER) and barcoded following the 7 cycle PCR with NEBNext ® Multiplex Oligos for Illumina ®.

    Reverse Transcription:

    Article Title: DNA-PKcs inhibitor AZD7648 reveals sgRNA cross-contaminants and enhanced sensitivity of genome engineering off-target activity in HSPCs.
    Article Snippet: .. The purified PCR amplicons were hen end repaired, A-tailed, ligated to an adapter, and purified ollowing the protocol in NEBNext ® UltraTM II DNA Library rep Kit for Illumina ® and NEBNext ® Multiplex Oligos for llumina ®. gRNA sequencing omplementary DNA (cDNA) of the sgRNAs were syntheized by mixing 200 ng sgRNA with 2 mM dNTP mix (Thermo Fisher), and 1 μM sgRNA scaffold specific primer (Merck) and incubated at 70 ◦C for 5 min. A reverse transcription mixture consisting of 1 × Template-Switching RT Buffer (NEB), Template-Switching RT Enzyme Mix (NEB), and 3.75 μM adapter-linked template-switching oligo (TSO) was then immediately added to the primer annealing mixture and incubated at 42 ◦C for 90 min and 85 ◦C for 5 min. sgRNA cDNA was diluted 1:10 and subjected to a nested PCR using 0.2 μM adapter-linked primer upstream of the original RT scaffold specific primer and Q5 Hot-start HF 2 × master mix (NEB). .. Amplicons were then purified using AMPure XP Bead-Based Reagent (BECKMAN COULTER) and barcoded following the 7 cycle PCR with NEBNext ® Multiplex Oligos for Illumina ®.

    Article Title: Alu-mediated RNA duplexes are associated with widespread exon skipping across primate transcriptomes
    Article Snippet: .. Reverse transcription was performed with SuperScript IV at 50 °C for 1 h using 1 μM 3′ adaptor–specific primer (5’ -TTCAGACGTGTGCTCTTCCGATCTATTGATGGTGCCTACAG-3’) and 1 μM template-switch oligo (TSO) containing a 10-nt unique molecular identifier (UMI) (5’ -CTT TCC CTA CAC GAC GCT CTT CCG ATCT NNNNNNNNNN TAC rGrGrG/3phos/−3’). cDNA fragments of 150–300nt were size-selected on a 6% urea-PAGE gel, then amplified with NEBNext Multiplex Oligos using Q5 DNA polymerase (NEB) for 12 cycles. .. cDNA fragments of 150–300nt were size-selected on a 6% urea-PAGE gel, then amplified with NEBNext Multiplex Oligos using Q5 DNA polymerase (NEB) for 12 cycles.

    Nested PCR:

    Article Title: DNA-PKcs inhibitor AZD7648 reveals sgRNA cross-contaminants and enhanced sensitivity of genome engineering off-target activity in HSPCs.
    Article Snippet: .. The purified PCR amplicons were hen end repaired, A-tailed, ligated to an adapter, and purified ollowing the protocol in NEBNext ® UltraTM II DNA Library rep Kit for Illumina ® and NEBNext ® Multiplex Oligos for llumina ®. gRNA sequencing omplementary DNA (cDNA) of the sgRNAs were syntheized by mixing 200 ng sgRNA with 2 mM dNTP mix (Thermo Fisher), and 1 μM sgRNA scaffold specific primer (Merck) and incubated at 70 ◦C for 5 min. A reverse transcription mixture consisting of 1 × Template-Switching RT Buffer (NEB), Template-Switching RT Enzyme Mix (NEB), and 3.75 μM adapter-linked template-switching oligo (TSO) was then immediately added to the primer annealing mixture and incubated at 42 ◦C for 90 min and 85 ◦C for 5 min. sgRNA cDNA was diluted 1:10 and subjected to a nested PCR using 0.2 μM adapter-linked primer upstream of the original RT scaffold specific primer and Q5 Hot-start HF 2 × master mix (NEB). .. Amplicons were then purified using AMPure XP Bead-Based Reagent (BECKMAN COULTER) and barcoded following the 7 cycle PCR with NEBNext ® Multiplex Oligos for Illumina ®.

    Methylation:

    Article Title: Molding the Rice Methylome for Disease Resistance
    Article Snippet: High-purity genomic DNA was extracted using IllustraTM NucleonTM PhytoPureTM kit (Cytiva), then sheared to ∼500bp fragments through sonication using Covaris M220. .. Enzymatic conversion of methylated cytosines and library preparation were performed using NEBNext® Enzymatic Methyl-seq Kit and NEBNext® Multiplex Oligos for Enzymatic Methyl-seq (New England Biolabs) according to the provided instructions, using sodium hydroxide for DNA denaturation and performing libraries size selection (470-520bp) for enrichment of larger inserts. .. Libraries were sequenced on Illumina NovaSeq X Plus using 2x 150bp paired-end configuration.

    Size Selection:

    Article Title: Molding the Rice Methylome for Disease Resistance
    Article Snippet: High-purity genomic DNA was extracted using IllustraTM NucleonTM PhytoPureTM kit (Cytiva), then sheared to ∼500bp fragments through sonication using Covaris M220. .. Enzymatic conversion of methylated cytosines and library preparation were performed using NEBNext® Enzymatic Methyl-seq Kit and NEBNext® Multiplex Oligos for Enzymatic Methyl-seq (New England Biolabs) according to the provided instructions, using sodium hydroxide for DNA denaturation and performing libraries size selection (470-520bp) for enrichment of larger inserts. .. Libraries were sequenced on Illumina NovaSeq X Plus using 2x 150bp paired-end configuration.

    Amplification:

    Article Title: Alu-mediated RNA duplexes are associated with widespread exon skipping across primate transcriptomes
    Article Snippet: .. Reverse transcription was performed with SuperScript IV at 50 °C for 1 h using 1 μM 3′ adaptor–specific primer (5’ -TTCAGACGTGTGCTCTTCCGATCTATTGATGGTGCCTACAG-3’) and 1 μM template-switch oligo (TSO) containing a 10-nt unique molecular identifier (UMI) (5’ -CTT TCC CTA CAC GAC GCT CTT CCG ATCT NNNNNNNNNN TAC rGrGrG/3phos/−3’). cDNA fragments of 150–300nt were size-selected on a 6% urea-PAGE gel, then amplified with NEBNext Multiplex Oligos using Q5 DNA polymerase (NEB) for 12 cycles. .. cDNA fragments of 150–300nt were size-selected on a 6% urea-PAGE gel, then amplified with NEBNext Multiplex Oligos using Q5 DNA polymerase (NEB) for 12 cycles.

    Article Title: Cancer detection and classification using methylome analysis
    Article Snippet: Briefly, for MeDIP, the Diagenode MagMeDIP kit (Cat #C02010021) was used following the manufacturer's protocol with some modifications. .. The optimal number of cycles to amplify each library was determined through the use of qPCR, after which the samples were amplified using the KAPA HiFi Hotstart Mastermix and the NEBNext multiplex oligos added to a final concentration of 0.3 μM. ..

    Article Title: HM-DyadCap - capture and mapping of 5-hydroxymethylcytosine/5-methylcytosine CpG dyads in mammalian DNA.
    Article Snippet: .. Preparation of Illumina libraries and NGS sequencing Enriched DNA fragments were PCR amplified using the NEBNext Ultra II DNA Library Prep Kit for Illumina (NEB, version 6.1_5/20) using NEBNext Multiplex Oligos (NEB, E73359). ..

    Article Title: HM-DyadCap – capture and mapping of 5-hydroxymethylcytosine/5-methylcytosine CpG dyads in mammalian DNA
    Article Snippet: .. Enriched DNA fragments were PCR amplified using the NEBNext Ultra II DNA Library Prep Kit for Illumina (NEB, version 6.1_5/20) using NEBNext Multiplex Oligos (NEB, E73359). ..

    Generated:

    Article Title: Epigenetic control of S100A8/A9-driven monocytic inflammation licenses anti-leukemic functionality of immature NK cells during hematopoietic stem cell differentiation
    Article Snippet: .. Libraries were generated from total RNA after poly(A)^+^ mRNA enrichment using the NEBNext Ultra II Directional RNA Library Prep Kit with NEBNext Multiplex Oligos (NEB) according to the manufacturer’s instructions. .. Sequencing was performed on an Illumina NovaSeq 6000 using 150 bp paired-end reads.

    Real-time Polymerase Chain Reaction:

    Article Title: Cancer detection and classification using methylome analysis
    Article Snippet: Briefly, for MeDIP, the Diagenode MagMeDIP kit (Cat #C02010021) was used following the manufacturer's protocol with some modifications. .. The optimal number of cycles to amplify each library was determined through the use of qPCR, after which the samples were amplified using the KAPA HiFi Hotstart Mastermix and the NEBNext multiplex oligos added to a final concentration of 0.3 μM. ..

    Concentration Assay:

    Article Title: Cancer detection and classification using methylome analysis
    Article Snippet: Briefly, for MeDIP, the Diagenode MagMeDIP kit (Cat #C02010021) was used following the manufacturer's protocol with some modifications. .. The optimal number of cycles to amplify each library was determined through the use of qPCR, after which the samples were amplified using the KAPA HiFi Hotstart Mastermix and the NEBNext multiplex oligos added to a final concentration of 0.3 μM. ..

    Hybridization:

    Article Title: deluxpore: a Nextflow pipeline for demultiplexing Illumina dual-indexed Nanopore libraries
    Article Snippet: .. As a solution, target enrichment can be performed on Illumina-indexed libraries, whereby dual indexes incorporated during library preparation allow samples to be pooled prior to capture hybridisation, after which the enriched pool is converted into a Nanopore-compatible library for MinION sequencing; a strategy recently applied to microbial gene capture using NEBNext Multiplex Oligos ( ). .. Importantly, this hybrid approach lacks practical implementation: standard Illumina demultiplexers cannot process Nanopore-derived data.

    Next-Generation Sequencing:

    Article Title: HM-DyadCap - capture and mapping of 5-hydroxymethylcytosine/5-methylcytosine CpG dyads in mammalian DNA.
    Article Snippet: .. Preparation of Illumina libraries and NGS sequencing Enriched DNA fragments were PCR amplified using the NEBNext Ultra II DNA Library Prep Kit for Illumina (NEB, version 6.1_5/20) using NEBNext Multiplex Oligos (NEB, E73359). ..



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    Image Search Results


    Journal: iScience

    Article Title: Gapmers targeting conserved SARS-CoV-2 single-stranded regions reduce viral load and reshape inflammatory macrophage responses

    doi: 10.1016/j.isci.2026.117639

    Figure Lengend Snippet:

    Article Snippet: NEBNext Multiplex Oligos for Illum , NEB , E7600.

    Techniques: Virus, Variant Assay, Recombinant, Reverse Transcription, Diagnostic Assay, Luminex, Ligation, Multiplex Assay, Generated, Software

    Journal: iScience

    Article Title: Gapmers targeting conserved SARS-CoV-2 single-stranded regions reduce viral load and reshape inflammatory macrophage responses

    doi: 10.1016/j.isci.2026.117639

    Figure Lengend Snippet:

    Article Snippet: Libraries were prepared by blunting and dA-tailing the amplicons using the End Prep library kit (NEB; Ref: E7546) followed by NEBNext Ultra II Ligation Module kit (NEB, Ref: E7595) with the adapters obtained from NEBNext Multiplex Oligos for Illumina (NEB, Ref:E7600) following standard protocols.

    Techniques: Virus, Variant Assay, Recombinant, Reverse Transcription, Diagnostic Assay, Luminex, Ligation, Multiplex Assay, Generated, Software