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5x protoscript ii reaction buffer  (New England Biolabs)


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    Structured Review

    New England Biolabs 5x protoscript ii reaction buffer
    5x Protoscript Ii Reaction Buffer, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 98/100, based on 1459 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/protoscript+ii+reverse+transcriptase+reaction+buffer/ProtoScript+II+Reverse+Transcriptase/pmc12804905-284-15-20
    Average 98 stars, based on 1459 article reviews
    5x protoscript ii reaction buffer - by Bioz Stars, 2026-10
    98/100 stars

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    Related Articles

    Reverse Transcription:

    Article Title: Off-target piRNA gene silencing in Drosophila melanogaster rescued by a transposable element insertion
    Article Snippet: The 5X RT Buffer comes with the ProtoScript® II Reverse Transcriptase (NEB, M0368X) and contains 250 mM Tris-HCl (pH 8.3), 375 mM KCl, 15 mM MgCl2. .. Comes with ProtoScript® II Reverse Transcriptase Reaction Buffer (NEB,M0368X) and is used in the RT reaction. .. No dilution necessary (Qiagen, 201900), comes as 10 mM stock.

    Article Title: CRISPR/Cas12a-Assisted Ligation-Initiated Loop-Mediated Isothermal Amplification (CAL-LAMP) for Highly Specific Detection of microRNAs.
    Article Snippet: Loop-mediated isothermal amplification (LAMP) has been increasingly applied in nucleic acid detection for clinical diagnosis and monitoring pathogenic microorganisms due to its isothermal nature and high sensitivity.. However, the false-positive signal resulting from the non-specific amplification and the complexity of primer design are still technically challenging for wide applications.. In this paper, we developed the CRISPR/ Cas12a-assisted sequence-specific detection of LAMP products to eliminate the effect of non-specific amplification from primer dimers and spurious amplicons.

    Article Title: Multiple Novel Human Norovirus Recombinants Identified in Wastewater in Pretoria, South Africa by Next-Generation Sequencing.
    Article Snippet: .. Complementary DNA was synthesised using 10 μL of the extracted nucleic acids, 30 μM random hexamers (Thermo Scientific), 0.5 mM dNTPs (New England Biolabs Inc., Ipswich, MA, USA), 1 × ProtoScript® II reverse transcriptase reaction buffer (New England Biolabs Inc.), 0.1 M DTT (New England Biolabs Inc.), 20 U RNase inhibitor (New England Biolabs Inc.), and 200 U ProtoScript® II reverse transcriptase (New England Biolabs Inc.). ..

    Article Title: Specific multiplexed detection of mRNA splice variants based on size-coding DNA probes and universal PCR amplification.
    Article Snippet: Alternative messenger RNA (mRNA) splicing is a vital regulatory process during the gene expression of higher eukaryotes.. The specific and sensitive quantification of disease-related mRNA splice variants in biological and clinical samples is becoming particularly important.. Reverse transcription polymerase chain reaction (RT-PCR), the most classical strategy for the assay of mRNA splice variants, cannot avoid false positive signals, which poses a challenge to the specificity of mRNA splice variant detection.

    Article Title: Alternative splicing coupled with transcript degradation modulates OAS1g antiviral activity
    Article Snippet: Following the stimulation, total RNA was isolated using Tri reagent solution and digested with DNase I (Invitrogen). .. RT reactions were performed in 20 μL (20 mM DTT, 2× ProtoScript II Reverse Transcriptase Reaction Buffer [NEB], 1 mM dNTPs, 40 U Murine RNase Inhibitor [NEB], and 200 U ProtoScript II [NEB] Reverse Transcriptase) with 500–1000 ng RNA. ..

    Article Title: Multiple Novel Human Norovirus Recombinants Identified in Wastewater in Pretoria, South Africa by Next-Generation Sequencing
    Article Snippet: .. Complementary DNA was synthesised using 10 μL of the extracted nucleic acids, 30 μM random hexamers (Thermo Scientific), 0.5 mM dNTPs (New England Biolabs Inc., Ipswich, MA, USA), 1 × ProtoScript ® II reverse transcriptase reaction buffer (New England Biolabs Inc.), 0.1 M DTT (New England Biolabs Inc.), 20 U RNase inhibitor (New England Biolabs Inc.), and 200 U ProtoScript ® II reverse transcriptase (New England Biolabs Inc.). ..

    Article Title: Mesophilic Argonaute-based isothermal detection of SARS-CoV-2
    Article Snippet: .. Briefly, 20 μl of reverse transcription reaction solution contained 0.5 mM deoxynucleotides (Sangon Biotech, Shanghai, China), 1 × ProtoScript ® II reverse transcriptase reaction buffer (New England Biolabs, MA, United States), 0.2 μM reverse transcription primer, 10 mM DTT, 8 units of RNase inhibitor (New England Biolabs, MA, United States), 200 units of ProtoScript ® II reverse transcriptase (New England Biolabs, MA, United States), and 1 μl of RNA sample or nuclease-free water (as a negative control). .. Reverse transcription reactions were performed at 42°C for 1 h. To the above reaction system, 5 units of RNase H (New England Biolabs, MA, United States) was added and incubated at 37°C for 20 min to degrade the RNA in the DNA-RNA hybrid strand.

    Negative Control:

    Article Title: Mesophilic Argonaute-based isothermal detection of SARS-CoV-2
    Article Snippet: .. Briefly, 20 μl of reverse transcription reaction solution contained 0.5 mM deoxynucleotides (Sangon Biotech, Shanghai, China), 1 × ProtoScript ® II reverse transcriptase reaction buffer (New England Biolabs, MA, United States), 0.2 μM reverse transcription primer, 10 mM DTT, 8 units of RNase inhibitor (New England Biolabs, MA, United States), 200 units of ProtoScript ® II reverse transcriptase (New England Biolabs, MA, United States), and 1 μl of RNA sample or nuclease-free water (as a negative control). .. Reverse transcription reactions were performed at 42°C for 1 h. To the above reaction system, 5 units of RNase H (New England Biolabs, MA, United States) was added and incubated at 37°C for 20 min to degrade the RNA in the DNA-RNA hybrid strand.



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