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protoscript ii first strand cdna synthesis kit  (New England Biolabs)


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    Structured Review

    New England Biolabs protoscript ii first strand cdna synthesis kit
    Protoscript Ii First Strand Cdna Synthesis Kit, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1853 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cdna/ProtoScript+II+First+Strand+cDNA+Synthesis+Kit/pm41832628-78-14-21
    Average 99 stars, based on 1853 article reviews
    protoscript ii first strand cdna synthesis kit - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    other:

    Article Title: The insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37
    Article Snippet: Oligonucleotides encoding the selected sgRNAs with overhangs compatible with BpiI restriction sites ( ) were annealed in vitro in Annealing buffer (5 mM Tris (#MB01601, NZYtech) pH 7.5–8, 25 mM NaCl (#MB15901, NZYtech) and 0.5 mM EDTA (#20302, VWR) by incubation at 95°C for 5 min, followed by a cool down until 85°C at 2°C/s and from 85°C to 25°C at 0.1°C/s.

    Article Title: The insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37.
    Article Snippet: Prior to zebrafish microinjection, each plasmid vector was purified with DNA Clean & Concentrator kit (#D4013, ZYMO Research) according to the manufacturer’s recommendations and resuspended in nuclease-free water.

    Purification:

    Article Title: NanoTS: a deep learning tool for accurate SNP calling in nanopore long-read transcriptome data.
    Article Snippet: .. Briefly, 120 ng of cDNA was repaired and dA-tailed using the NEBNext Ultra II End Repair/dA-tailing Module (NEB, cat. no. E7546L) followed by purification with DNA Clean Beads. .. For multiplexing, the repaired DNA was barcoded using the Native Barcode kit with NEB Blunt/TA Ligase Master Mix (NEB, cat. no. M0367S) and purified again with DNA Clean Beads.

    Polymerase Chain Reaction:

    Article Title: CXCR4-tropic HIV-1 infection in an immunocompetent monkey model.
    Article Snippet: 2.5 mL of blood were collected from naive colony animals in RNA preservation tubes (PAXgene Blood RNA Tube, BD Biosciences #762165) that were processed according to the manufacturer’s instructions. .. Genespecific primers (placed in the 5' and 3' UTRs) were then used to PCR-amplify cDNA nucleic acids encoding CD4, Tetherin, TRIMCyp, and APOBEC3G from cDNA using Q5 High-Fidelity DNA Polymerase (New England BioLabs #M0491L). .. RNA was isolated using TRIzol (Invitrogen #15596018) and cDNA libraries were AR TI CL E IN P RE SS prepared using the SuperScript IV First-Strand Synthesis System (Invitrogen #18091200).

    Article Title: Melatonin Protects Mouse Oocytes From the Environmental Toxicant 6PPD-Quinone by Preserving Mitochondrial and Endomembrane Homeostasis.
    Article Snippet: N‐(1,3‐dimethylbutyl)‐N′‐phenyl‐p‐phenylenediamine‐quinone (6PPD‐Q) is a ubiquitous tire‐derived transformation product with emerging reproductive toxicity; however, its impact on mammalian oocytes and the potential protective role of melatonin (MT) remain unclear.. Here, we evaluate 6PPD‐Q–induced impairment of mouse oocyte competence and assess the protective efficacy of MT.. 6PPD‐Q exposure significantly decreases polar body extrusion, fertilization, and 2‐cell embryo formation, whereas MT co‐treatment markedly restores these developmental outcomes.

    Article Title: microRNAs bidirectionally regulate FUT1 to modulate α-1,2-fucosylation and cancer-associated biology
    Article Snippet: .. FUT1 3’UTR (ENST00000310160.3, 2173 nucleotides) was amplified from cDNA (MCF7 cell line) using Q5 High-Fidelity DNA polymerase (Cat# M0492L, New England Biolabs (NEB)) according to PCR conditions provided by the company. .. NheI and BamHI restriction sites were used for cloning FUT1 3’UTR downstream of Cerulean in pFmiR-empty backbone using the standard NEB ligation protocol.

    Amplification:

    Article Title: Melatonin Protects Mouse Oocytes From the Environmental Toxicant 6PPD-Quinone by Preserving Mitochondrial and Endomembrane Homeostasis.
    Article Snippet: N‐(1,3‐dimethylbutyl)‐N′‐phenyl‐p‐phenylenediamine‐quinone (6PPD‐Q) is a ubiquitous tire‐derived transformation product with emerging reproductive toxicity; however, its impact on mammalian oocytes and the potential protective role of melatonin (MT) remain unclear.. Here, we evaluate 6PPD‐Q–induced impairment of mouse oocyte competence and assess the protective efficacy of MT.. 6PPD‐Q exposure significantly decreases polar body extrusion, fertilization, and 2‐cell embryo formation, whereas MT co‐treatment markedly restores these developmental outcomes.

    Article Title: microRNAs bidirectionally regulate FUT1 to modulate α-1,2-fucosylation and cancer-associated biology
    Article Snippet: .. FUT1 3’UTR (ENST00000310160.3, 2173 nucleotides) was amplified from cDNA (MCF7 cell line) using Q5 High-Fidelity DNA polymerase (Cat# M0492L, New England Biolabs (NEB)) according to PCR conditions provided by the company. .. NheI and BamHI restriction sites were used for cloning FUT1 3’UTR downstream of Cerulean in pFmiR-empty backbone using the standard NEB ligation protocol.

    Article Title: Flamenco plasticity tunes somatic piRNAs and rewires isoforms, with implications for heritable transposon spread
    Article Snippet: Reverse transcription was performed with the Transcriptor First Strand cDNA Synthesis Kit (Roche) using oligo(dT) primers. .. The resulting cDNA was amplified with Q5 High-Fidelity DNA Polymerase (New England Biolabs). .. PCR products were resolved on a 1% TBE agarose gel, stained with SYBR Gold (Thermo Fisher Scientific) for 10 min, and visualized with a transilluminator ( ).

    Ligation:

    Article Title: Melatonin Protects Mouse Oocytes From the Environmental Toxicant 6PPD-Quinone by Preserving Mitochondrial and Endomembrane Homeostasis.
    Article Snippet: N‐(1,3‐dimethylbutyl)‐N′‐phenyl‐p‐phenylenediamine‐quinone (6PPD‐Q) is a ubiquitous tire‐derived transformation product with emerging reproductive toxicity; however, its impact on mammalian oocytes and the potential protective role of melatonin (MT) remain unclear.. Here, we evaluate 6PPD‐Q–induced impairment of mouse oocyte competence and assess the protective efficacy of MT.. 6PPD‐Q exposure significantly decreases polar body extrusion, fertilization, and 2‐cell embryo formation, whereas MT co‐treatment markedly restores these developmental outcomes.

    Construct:

    Article Title: Pervasive enhanced transcription in inflammatory breast cancer tumors and PBMCs impacts RNA splicing and intronic RNAs in plasma
    Article Snippet: .. TGIRT-seq libraries were constructed as described ( , ) by using TGIRT-template switching from a synthetic RNA template/DNA primer duplex to the 3′ end of the target RNA for 3′ RNA-seq adapter addition and a single-stranded DNA ligation to the 3′ end of the cDNA using Thermostable 5′ AppDNA/RNA Ligase (New England Biolabs) for 5′ RNA-seq adapter addition. .. The TGIRT template-switching reaction was done with 1 μM TGIRT-III RT (InGex, LLC) for 15 min at 60°C.

    RNA Sequencing:

    Article Title: Pervasive enhanced transcription in inflammatory breast cancer tumors and PBMCs impacts RNA splicing and intronic RNAs in plasma
    Article Snippet: .. TGIRT-seq libraries were constructed as described ( , ) by using TGIRT-template switching from a synthetic RNA template/DNA primer duplex to the 3′ end of the target RNA for 3′ RNA-seq adapter addition and a single-stranded DNA ligation to the 3′ end of the cDNA using Thermostable 5′ AppDNA/RNA Ligase (New England Biolabs) for 5′ RNA-seq adapter addition. .. The TGIRT template-switching reaction was done with 1 μM TGIRT-III RT (InGex, LLC) for 15 min at 60°C.

    DNA Ligation:

    Article Title: Pervasive enhanced transcription in inflammatory breast cancer tumors and PBMCs impacts RNA splicing and intronic RNAs in plasma
    Article Snippet: .. TGIRT-seq libraries were constructed as described ( , ) by using TGIRT-template switching from a synthetic RNA template/DNA primer duplex to the 3′ end of the target RNA for 3′ RNA-seq adapter addition and a single-stranded DNA ligation to the 3′ end of the cDNA using Thermostable 5′ AppDNA/RNA Ligase (New England Biolabs) for 5′ RNA-seq adapter addition. .. The TGIRT template-switching reaction was done with 1 μM TGIRT-III RT (InGex, LLC) for 15 min at 60°C.



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    Image Search Results


    Journal: iScience

    Article Title: Rhizobacterial biocontrol of potato late blight and genomic insights into disease suppression and growth promotion

    doi: 10.1016/j.isci.2026.117682

    Figure Lengend Snippet:

    Article Snippet: qScript cDNA Synthesis Kit , Quantabio , Cat#95047-100.

    Techniques: Recombinant, cDNA Synthesis, Software