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script reverse transcriptase mix  (Jena Bioscience)


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    Structured Review

    Jena Bioscience script reverse transcriptase mix
    Script Reverse Transcriptase Mix, supplied by Jena Bioscience, used in various techniques. Bioz Stars score: 94/100, based on 29 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/reverse+transcriptase+mixture/SCRIPT+Reverse+Transcriptase/pm42283997-76-8-12
    Average 94 stars, based on 29 article reviews
    script reverse transcriptase mix - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    other:

    Article Title: Use of allele-specific qPCR and PCR-RFLP analysis for rapid detection of the SARS-CoV-2 variants in Tunisia: A cheap flexible approach adapted for developing countries.
    Article Snippet: The PCR products were cloned in a pGEM-T vector (Promega), and then transformed into E. coli.

    Spectroscopy:

    Article Title: Immunohistochemical analysis of YB-1 expression in the developing mouse eye.
    Article Snippet: Briefly, tissue was homogenized in lysis buffer (Macherey and Nagel Nucleospin RNA/Protein kit), and RNA and protein was prepared according to the manufacturer’s recommendations. .. RNA was quantified by UV spectroscopy, and cDNA was synthesized from 500 ng using anchored oligo-dT-primer and Script reverse transcriptase, following the manufacturer’s (Jena Bioscience, Jena, Germany) manual. .. PCR was performed using YourTaq DirectLoad PCR Mix (biotechrabbit, Berlin, Germany) in 30 cycles (96°C for 20 s; 60°C for 20 s; 72°C for 1 min, with a final 10 min extension at 72°C) using the following primers (Eurofins MWG Operon, Ebersberg, Germany): fw1: GGAGAAGTGATGGAGGGTGC; rev1: GGTTTAGGGTTCTCTGGGCG; fw2: AGAACGAGGGATCGGAAAGC; rev2: TGCCATCCTCTCTAGGCTGT.

    Synthesized:

    Article Title: Immunohistochemical analysis of YB-1 expression in the developing mouse eye.
    Article Snippet: Briefly, tissue was homogenized in lysis buffer (Macherey and Nagel Nucleospin RNA/Protein kit), and RNA and protein was prepared according to the manufacturer’s recommendations. .. RNA was quantified by UV spectroscopy, and cDNA was synthesized from 500 ng using anchored oligo-dT-primer and Script reverse transcriptase, following the manufacturer’s (Jena Bioscience, Jena, Germany) manual. .. PCR was performed using YourTaq DirectLoad PCR Mix (biotechrabbit, Berlin, Germany) in 30 cycles (96°C for 20 s; 60°C for 20 s; 72°C for 1 min, with a final 10 min extension at 72°C) using the following primers (Eurofins MWG Operon, Ebersberg, Germany): fw1: GGAGAAGTGATGGAGGGTGC; rev1: GGTTTAGGGTTCTCTGGGCG; fw2: AGAACGAGGGATCGGAAAGC; rev2: TGCCATCCTCTCTAGGCTGT.

    Article Title: Interplay of Interleukin-1 β and Curcumin on VEGF Expression in Breast Cancer Cells
    Article Snippet: RNA was extracted from cell cultures using the NucleoSpin RNA kit (#704933, Macherey-Nagel, Düren, Germany) according to the manufacturer’s recommendations. .. cDNA was synthesized using Script Reverse Transcriptase and oligo dT primers from 1 μg of total RNA (# PCR505 and # PM305, Jenabioscience, Jena, Germany). .. Real-time PCR was performed in a 20 μL volume using a Roche LightCycler 1.0 and the LightCycler FastStart DNA Master SYBR Green I reagents (#03003230001, Roche-Life Science, Mannheim, Germany).

    Reverse Transcription:

    Article Title: Immunohistochemical analysis of YB-1 expression in the developing mouse eye.
    Article Snippet: Briefly, tissue was homogenized in lysis buffer (Macherey and Nagel Nucleospin RNA/Protein kit), and RNA and protein was prepared according to the manufacturer’s recommendations. .. RNA was quantified by UV spectroscopy, and cDNA was synthesized from 500 ng using anchored oligo-dT-primer and Script reverse transcriptase, following the manufacturer’s (Jena Bioscience, Jena, Germany) manual. .. PCR was performed using YourTaq DirectLoad PCR Mix (biotechrabbit, Berlin, Germany) in 30 cycles (96°C for 20 s; 60°C for 20 s; 72°C for 1 min, with a final 10 min extension at 72°C) using the following primers (Eurofins MWG Operon, Ebersberg, Germany): fw1: GGAGAAGTGATGGAGGGTGC; rev1: GGTTTAGGGTTCTCTGGGCG; fw2: AGAACGAGGGATCGGAAAGC; rev2: TGCCATCCTCTCTAGGCTGT.

    Article Title: Interplay of Interleukin-1 β and Curcumin on VEGF Expression in Breast Cancer Cells
    Article Snippet: RNA was extracted from cell cultures using the NucleoSpin RNA kit (#704933, Macherey-Nagel, Düren, Germany) according to the manufacturer’s recommendations. .. cDNA was synthesized using Script Reverse Transcriptase and oligo dT primers from 1 μg of total RNA (# PCR505 and # PM305, Jenabioscience, Jena, Germany). .. Real-time PCR was performed in a 20 μL volume using a Roche LightCycler 1.0 and the LightCycler FastStart DNA Master SYBR Green I reagents (#03003230001, Roche-Life Science, Mannheim, Germany).

    Article Title: Using Moss Walls for Air Quality Monitoring: Extending Their Utility Beyond Traditional Green Infrastructure
    Article Snippet: .. RT-qPCR For the analysis of rbcL gene expression, 1 μg of total RNA was reverse transcribed into cDNA using Script cDNA polymerase (Jena Bioscience, Jena, Germany) following the manufacturer’s protocol. .. RT-qPCR was conducted in triplicate using an Applied Biosystems 7500 Real-Time PCR System and the Green Master Mix Kit (Genaxxon Bioscience, Ulm, Germany) in a reaction volume of 25 μL.

    Article Title: Detection of flaviviruses in mosquitoes from a livestock farm in Ibadan, Nigeria.
    Article Snippet: Orthoflaviviruses constitute a diverse genus within the Flaviviridae family, comprising over 70 enveloped, single-stranded positive-sense RNA viruses that pose significant global health threats.. Yellow fever virus (YFV) remains a significant public health concern in Nigeria, with suboptimal vaccination coverage and a persistent risk of transmission.. Understanding the circulation of local orthoflaviviruses in mosquito vectors is crucial for disease surveillance and prevention strategies.

    Article Title: Use of allele-specific qPCR and PCR-RFLP analysis for rapid detection of the SARS-CoV-2 variants in Tunisia: A cheap flexible approach adapted for developing countries
    Article Snippet: The concentration of each recombinant plasmid was determined by Nanodrop (Spectrophotometer 2000) and the corresponding copy number (copies/μL) was calculated using the following equation: Finally, serial ten-fold dilutions of each recombinant plasmid with a known copy number was generated and used as standards for the corresponding AS-qPCR or PCR-RFLP screening assay. .. First-strand cDNA synthesis was prepared from 4 μl of RNA extract in a final volume of 20 μl containing 1× reaction buffer, 0.2 pmol of each of the specific Reverse primers , 20 nmol of each dNTP, 0.2 μmol of DTT and 100 U of SCRIPT Reverse Transcriptase (Jena Bioscience). ..

    Article Title: The farnesoid X receptor activates transcription independently of RXR at non-canonical response elements
    Article Snippet: The Nano-Glo Live Cell Assay System (Promega, N2012) was used according to the manufacturer’s protocol. .. For reverse transcription followed by qPCR, 500 ng total RNA was reverse transcribed with random hexamers using SCRIPT (Jena biosciences). .. RNA was isolated from HepG2 cells after 8 h treatment (4 μM HX531 + 10 μM OCA) for quantitative PCR (qPCR) analysis, or 16 h treatment (10 μM OCA) for RNA-seq using TRIzol reagent (LifeTechnologies, Naugatuck, CT) according to the manufacturer’s protocol.

    Quantitative RT-PCR:

    Article Title: Using Moss Walls for Air Quality Monitoring: Extending Their Utility Beyond Traditional Green Infrastructure
    Article Snippet: .. RT-qPCR For the analysis of rbcL gene expression, 1 μg of total RNA was reverse transcribed into cDNA using Script cDNA polymerase (Jena Bioscience, Jena, Germany) following the manufacturer’s protocol. .. RT-qPCR was conducted in triplicate using an Applied Biosystems 7500 Real-Time PCR System and the Green Master Mix Kit (Genaxxon Bioscience, Ulm, Germany) in a reaction volume of 25 μL.

    Analysis:

    Article Title: Using Moss Walls for Air Quality Monitoring: Extending Their Utility Beyond Traditional Green Infrastructure
    Article Snippet: .. RT-qPCR For the analysis of rbcL gene expression, 1 μg of total RNA was reverse transcribed into cDNA using Script cDNA polymerase (Jena Bioscience, Jena, Germany) following the manufacturer’s protocol. .. RT-qPCR was conducted in triplicate using an Applied Biosystems 7500 Real-Time PCR System and the Green Master Mix Kit (Genaxxon Bioscience, Ulm, Germany) in a reaction volume of 25 μL.

    Gene Expression:

    Article Title: Using Moss Walls for Air Quality Monitoring: Extending Their Utility Beyond Traditional Green Infrastructure
    Article Snippet: .. RT-qPCR For the analysis of rbcL gene expression, 1 μg of total RNA was reverse transcribed into cDNA using Script cDNA polymerase (Jena Bioscience, Jena, Germany) following the manufacturer’s protocol. .. RT-qPCR was conducted in triplicate using an Applied Biosystems 7500 Real-Time PCR System and the Green Master Mix Kit (Genaxxon Bioscience, Ulm, Germany) in a reaction volume of 25 μL.

    One Step RT-PCR:

    Article Title: Detection of flaviviruses in mosquitoes from a livestock farm in Ibadan, Nigeria.
    Article Snippet: Orthoflaviviruses constitute a diverse genus within the Flaviviridae family, comprising over 70 enveloped, single-stranded positive-sense RNA viruses that pose significant global health threats.. Yellow fever virus (YFV) remains a significant public health concern in Nigeria, with suboptimal vaccination coverage and a persistent risk of transmission.. Understanding the circulation of local orthoflaviviruses in mosquito vectors is crucial for disease surveillance and prevention strategies.

    cDNA Synthesis:

    Article Title: Use of allele-specific qPCR and PCR-RFLP analysis for rapid detection of the SARS-CoV-2 variants in Tunisia: A cheap flexible approach adapted for developing countries
    Article Snippet: The concentration of each recombinant plasmid was determined by Nanodrop (Spectrophotometer 2000) and the corresponding copy number (copies/μL) was calculated using the following equation: Finally, serial ten-fold dilutions of each recombinant plasmid with a known copy number was generated and used as standards for the corresponding AS-qPCR or PCR-RFLP screening assay. .. First-strand cDNA synthesis was prepared from 4 μl of RNA extract in a final volume of 20 μl containing 1× reaction buffer, 0.2 pmol of each of the specific Reverse primers , 20 nmol of each dNTP, 0.2 μmol of DTT and 100 U of SCRIPT Reverse Transcriptase (Jena Bioscience). ..

    Real-time Polymerase Chain Reaction:

    Article Title: The farnesoid X receptor activates transcription independently of RXR at non-canonical response elements
    Article Snippet: The Nano-Glo Live Cell Assay System (Promega, N2012) was used according to the manufacturer’s protocol. .. For reverse transcription followed by qPCR, 500 ng total RNA was reverse transcribed with random hexamers using SCRIPT (Jena biosciences). .. RNA was isolated from HepG2 cells after 8 h treatment (4 μM HX531 + 10 μM OCA) for quantitative PCR (qPCR) analysis, or 16 h treatment (10 μM OCA) for RNA-seq using TRIzol reagent (LifeTechnologies, Naugatuck, CT) according to the manufacturer’s protocol.



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