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reverse transcriptase kit  (TaKaRa)


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    Structured Review

    TaKaRa reverse transcriptase kit
    Reverse Transcriptase Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 2331 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cdna+reverse+transcriptase+kit/PrimeScript+1st+strand+cDNA+Synthesis+Kit/us12600957-257-0-12
    Average 99 stars, based on 2331 article reviews
    reverse transcriptase kit - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Reverse Transcription:

    Article Title: Estrogen Receptor-α36 Mediates EGFR-SGK1 Signaling-Related Erk Activation in Gastric Cancer.
    Article Snippet: .. One microgram of RNA was reverse-transcribed into cDNA using the PrimeScript II 1st Strand cDNA Synthesis Kit (Takara, 6210A, Kusatsu, Japan). qRT-PCR was performed using TB Green https://doi.org/10.3390/cells15090787 Fast qPCR Mix (Takara, RR420) on a CFX96 real-time PCR system (Applied Biosystems, Foster City, CA, USA). ..

    Article Title: IL-15 and IL-21 synergy improves anti-tumor efficacy of iPSC-derived cytotoxic T cells in solid tumors.
    Article Snippet: .. We reverse transcribed mRNA using a PrimeScriptII 1st Strand cDNA Synthesis Kit (Takara). .. We amplified the cytokine-encoding genes using KOD Plus NEO enzyme (Toyobo, Japan).

    Article Title: Exon skipping by peptide nucleic acid derivatives
    Article Snippet: Then the culture medium was replaced with fresh medium, and treated with “PD-ASO 3” at 0 (negative control), 10, 100 or 1,000 aM for 24 hours. (4 culture dishes per ASO concentration) [RNA Extraction and cDNA Synthesis] Total RNA was extracted using RNeasy mini prep kit (Qiagen, USA) according to the manufacturer's protocol. .. 500 ng of RNA template was subjected to a 25 μL reverse transcription reaction using PrimeScriptTM 1st strand cDNA synthesis kit (Takara, Japan) according to the manufacturer's protocol. ..

    cDNA Synthesis:

    Article Title: Estrogen Receptor-α36 Mediates EGFR-SGK1 Signaling-Related Erk Activation in Gastric Cancer.
    Article Snippet: .. One microgram of RNA was reverse-transcribed into cDNA using the PrimeScript II 1st Strand cDNA Synthesis Kit (Takara, 6210A, Kusatsu, Japan). qRT-PCR was performed using TB Green https://doi.org/10.3390/cells15090787 Fast qPCR Mix (Takara, RR420) on a CFX96 real-time PCR system (Applied Biosystems, Foster City, CA, USA). ..

    Article Title: Method of alleviating obsessive compulsive disorder symptoms by use of a multi-strain probiotic formulation
    Article Snippet: Briefly, NucleoSpin® RNA isolation kit (#740955.50, DSS Takara Bio India Private Ltd) was used to extract RNA from the rat brain's amygdala. .. PrimeScriptTM 1st strand cDNA synthesis kit (#6110A, DSS Takara Bio India Private Ltd) was used to process these RNA samples to cDNA. .. The 10 μL reaction mixture was prepared by mixing 5 μL of SYBR Green, 2 μL of the PCR primer (1 μL reverse+1 μL forward) (GCC Biotech, India, Private Ltd.).

    Article Title: Discovery of acyclic purine nucleosides as promising antiviral agents against dengue virus.
    Article Snippet: Dengue virus (DENV) remains a significant global health challenge as one of the most prevalent mosquito-borne viral infections, with no specific antiviral therapy currently approved.. Acyclic purine nucleosides have demonstrated as broad-spectrum antiviral activity by interfering with viral genome replication.. Therefore, in this study, we designed a new series of D-glucose-derived acyclic purine nucleoside analogues (5a-f, 6a-c, and 8a-b), and evaluated their inhibitory activity against DENV serotype 2 (DENV2) using an in vitro Huh-7 cell-based assay.

    Article Title: A novel hemizygous missense variant in the BEND2 gene is associated with nonobstructive azoospermia.
    Article Snippet: After the cells were washed with phosphatebuffered saline (PBS), the sections were incubated with Alexa Fluor 488-conjugated anti-rabbit IgG (A-11008; 1:500; Invitrogen, Carlsbad, CA, USA) and peanut agglutinin (PNA; CL-1073-1; 1:500; Vector Labs, Burlingame, CA, USA) for 2 h at room temperature, after which the nuclei were counterstained with Hoechst 33342 (H3570; 1:5000; Invitrogen). .. Imaging was performed on a Zeiss LSM 980 confocal system (ZEISS, Oberkochen, Germany). mRNA expression analysis Total RNA was isolated from the peripheral blood of the NOA proband and OA control, after which first-strand complementary DNA (cDNA) synthesis was performed using a Takara PrimeScript RT Reagent Kit (6110A; Takara, Otsu, Japan) with random hexamers. .. Reverse transcription quantitative polymerase chain reaction (RT‒qPCR) was performed on a Bio-Rad CFX96 system with Takara TB Green Premix Ex Taq II (RR420A; Takara), with the following thermal cycling conditions: initial denaturation (95°C for 30 s), 40 cycles of 95°C for 5 s; and 60°C for 30 s. Relative BEND2 mRNA expressions were quantified via the 2−ΔCt method and normalized to that of glyceraldehyde-3phosphate dehydrogenase (GAPDH) using the following primers: BEND2 forward, 5’-CCAATTTGGAATCTGGCCCAC-3’, and BEND2 reverse, 5’-GGCCACTGTCACTGTCCAAT-3’; and GAPDH forward, 5’-GGAGCGAGATCCCTCCAAAAT-3’, and GAPDH reverse, 5’-GGCTGTTGTCATACTTCTCATGG-3’.

    Article Title: High Fat Diet‐Induced Obesity Alters Cutaneous Immune Cell Function, and These Changes Persist After Weight Loss
    Article Snippet: Total RNA was extracted from the tissues using ISOGEN (Nippon Gene CO. Ltd., Tokyo, Japan). .. Complementary deoxyribonucleic acid (cDNA) was synthesized using the PrimeScript 1st‐standard cDNA synthesis kit (TaKaRa Bio Inc., Otsu, Japan) according to the manufacturer’s instructions. .. Real‐time quantitative PCR was performed using gene‐specific primers and FastStart essential DNA green master mix (Sigma–Aldrich, St. Louis, MO, USA) on a StepOnePlus Real‐Time PCR System (Thermo Fisher Scientific, Inc., Waltham, USA).

    Article Title: IL-15 and IL-21 synergy improves anti-tumor efficacy of iPSC-derived cytotoxic T cells in solid tumors.
    Article Snippet: .. We reverse transcribed mRNA using a PrimeScriptII 1st Strand cDNA Synthesis Kit (Takara). .. We amplified the cytokine-encoding genes using KOD Plus NEO enzyme (Toyobo, Japan).

    Article Title: Dual-compartment engagement of STAR-family proteins SAM68 and QKI by LINC00941 sustains oncogenic fitness in RAS-driven lung cancer
    Article Snippet: RNA quantity and integrity were assessed by NanoDrop spectrophotometry and agarose gel electrophoresis, respectively. .. Complementary DNA (cDNA) was synthesised from 500 ng–1 μ g total RNA using the PrimeScriptTM 1st-strand cDNA Synthesis Kit (Takara Bio, Japan). .. Quantitative PCR was performed on a Bio-Rad qPCR system using SYBR Green Master Mix (Thermo Scientific).

    Article Title: Exon skipping by peptide nucleic acid derivatives
    Article Snippet: Then the culture medium was replaced with fresh medium, and treated with “PD-ASO 3” at 0 (negative control), 10, 100 or 1,000 aM for 24 hours. (4 culture dishes per ASO concentration) [RNA Extraction and cDNA Synthesis] Total RNA was extracted using RNeasy mini prep kit (Qiagen, USA) according to the manufacturer's protocol. .. 500 ng of RNA template was subjected to a 25 μL reverse transcription reaction using PrimeScriptTM 1st strand cDNA synthesis kit (Takara, Japan) according to the manufacturer's protocol. ..

    Quantitative RT-PCR:

    Article Title: Estrogen Receptor-α36 Mediates EGFR-SGK1 Signaling-Related Erk Activation in Gastric Cancer.
    Article Snippet: .. One microgram of RNA was reverse-transcribed into cDNA using the PrimeScript II 1st Strand cDNA Synthesis Kit (Takara, 6210A, Kusatsu, Japan). qRT-PCR was performed using TB Green https://doi.org/10.3390/cells15090787 Fast qPCR Mix (Takara, RR420) on a CFX96 real-time PCR system (Applied Biosystems, Foster City, CA, USA). ..

    Real-time Polymerase Chain Reaction:

    Article Title: Estrogen Receptor-α36 Mediates EGFR-SGK1 Signaling-Related Erk Activation in Gastric Cancer.
    Article Snippet: .. One microgram of RNA was reverse-transcribed into cDNA using the PrimeScript II 1st Strand cDNA Synthesis Kit (Takara, 6210A, Kusatsu, Japan). qRT-PCR was performed using TB Green https://doi.org/10.3390/cells15090787 Fast qPCR Mix (Takara, RR420) on a CFX96 real-time PCR system (Applied Biosystems, Foster City, CA, USA). ..

    Isolation:

    Article Title: Discovery of acyclic purine nucleosides as promising antiviral agents against dengue virus.
    Article Snippet: Dengue virus (DENV) remains a significant global health challenge as one of the most prevalent mosquito-borne viral infections, with no specific antiviral therapy currently approved.. Acyclic purine nucleosides have demonstrated as broad-spectrum antiviral activity by interfering with viral genome replication.. Therefore, in this study, we designed a new series of D-glucose-derived acyclic purine nucleoside analogues (5a-f, 6a-c, and 8a-b), and evaluated their inhibitory activity against DENV serotype 2 (DENV2) using an in vitro Huh-7 cell-based assay.

    Article Title: A novel hemizygous missense variant in the BEND2 gene is associated with nonobstructive azoospermia.
    Article Snippet: After the cells were washed with phosphatebuffered saline (PBS), the sections were incubated with Alexa Fluor 488-conjugated anti-rabbit IgG (A-11008; 1:500; Invitrogen, Carlsbad, CA, USA) and peanut agglutinin (PNA; CL-1073-1; 1:500; Vector Labs, Burlingame, CA, USA) for 2 h at room temperature, after which the nuclei were counterstained with Hoechst 33342 (H3570; 1:5000; Invitrogen). .. Imaging was performed on a Zeiss LSM 980 confocal system (ZEISS, Oberkochen, Germany). mRNA expression analysis Total RNA was isolated from the peripheral blood of the NOA proband and OA control, after which first-strand complementary DNA (cDNA) synthesis was performed using a Takara PrimeScript RT Reagent Kit (6110A; Takara, Otsu, Japan) with random hexamers. .. Reverse transcription quantitative polymerase chain reaction (RT‒qPCR) was performed on a Bio-Rad CFX96 system with Takara TB Green Premix Ex Taq II (RR420A; Takara), with the following thermal cycling conditions: initial denaturation (95°C for 30 s), 40 cycles of 95°C for 5 s; and 60°C for 30 s. Relative BEND2 mRNA expressions were quantified via the 2−ΔCt method and normalized to that of glyceraldehyde-3phosphate dehydrogenase (GAPDH) using the following primers: BEND2 forward, 5’-CCAATTTGGAATCTGGCCCAC-3’, and BEND2 reverse, 5’-GGCCACTGTCACTGTCCAAT-3’; and GAPDH forward, 5’-GGAGCGAGATCCCTCCAAAAT-3’, and GAPDH reverse, 5’-GGCTGTTGTCATACTTCTCATGG-3’.

    Imaging:

    Article Title: A novel hemizygous missense variant in the BEND2 gene is associated with nonobstructive azoospermia.
    Article Snippet: After the cells were washed with phosphatebuffered saline (PBS), the sections were incubated with Alexa Fluor 488-conjugated anti-rabbit IgG (A-11008; 1:500; Invitrogen, Carlsbad, CA, USA) and peanut agglutinin (PNA; CL-1073-1; 1:500; Vector Labs, Burlingame, CA, USA) for 2 h at room temperature, after which the nuclei were counterstained with Hoechst 33342 (H3570; 1:5000; Invitrogen). .. Imaging was performed on a Zeiss LSM 980 confocal system (ZEISS, Oberkochen, Germany). mRNA expression analysis Total RNA was isolated from the peripheral blood of the NOA proband and OA control, after which first-strand complementary DNA (cDNA) synthesis was performed using a Takara PrimeScript RT Reagent Kit (6110A; Takara, Otsu, Japan) with random hexamers. .. Reverse transcription quantitative polymerase chain reaction (RT‒qPCR) was performed on a Bio-Rad CFX96 system with Takara TB Green Premix Ex Taq II (RR420A; Takara), with the following thermal cycling conditions: initial denaturation (95°C for 30 s), 40 cycles of 95°C for 5 s; and 60°C for 30 s. Relative BEND2 mRNA expressions were quantified via the 2−ΔCt method and normalized to that of glyceraldehyde-3phosphate dehydrogenase (GAPDH) using the following primers: BEND2 forward, 5’-CCAATTTGGAATCTGGCCCAC-3’, and BEND2 reverse, 5’-GGCCACTGTCACTGTCCAAT-3’; and GAPDH forward, 5’-GGAGCGAGATCCCTCCAAAAT-3’, and GAPDH reverse, 5’-GGCTGTTGTCATACTTCTCATGG-3’.

    Expressing:

    Article Title: A novel hemizygous missense variant in the BEND2 gene is associated with nonobstructive azoospermia.
    Article Snippet: After the cells were washed with phosphatebuffered saline (PBS), the sections were incubated with Alexa Fluor 488-conjugated anti-rabbit IgG (A-11008; 1:500; Invitrogen, Carlsbad, CA, USA) and peanut agglutinin (PNA; CL-1073-1; 1:500; Vector Labs, Burlingame, CA, USA) for 2 h at room temperature, after which the nuclei were counterstained with Hoechst 33342 (H3570; 1:5000; Invitrogen). .. Imaging was performed on a Zeiss LSM 980 confocal system (ZEISS, Oberkochen, Germany). mRNA expression analysis Total RNA was isolated from the peripheral blood of the NOA proband and OA control, after which first-strand complementary DNA (cDNA) synthesis was performed using a Takara PrimeScript RT Reagent Kit (6110A; Takara, Otsu, Japan) with random hexamers. .. Reverse transcription quantitative polymerase chain reaction (RT‒qPCR) was performed on a Bio-Rad CFX96 system with Takara TB Green Premix Ex Taq II (RR420A; Takara), with the following thermal cycling conditions: initial denaturation (95°C for 30 s), 40 cycles of 95°C for 5 s; and 60°C for 30 s. Relative BEND2 mRNA expressions were quantified via the 2−ΔCt method and normalized to that of glyceraldehyde-3phosphate dehydrogenase (GAPDH) using the following primers: BEND2 forward, 5’-CCAATTTGGAATCTGGCCCAC-3’, and BEND2 reverse, 5’-GGCCACTGTCACTGTCCAAT-3’; and GAPDH forward, 5’-GGAGCGAGATCCCTCCAAAAT-3’, and GAPDH reverse, 5’-GGCTGTTGTCATACTTCTCATGG-3’.

    Control:

    Article Title: A novel hemizygous missense variant in the BEND2 gene is associated with nonobstructive azoospermia.
    Article Snippet: After the cells were washed with phosphatebuffered saline (PBS), the sections were incubated with Alexa Fluor 488-conjugated anti-rabbit IgG (A-11008; 1:500; Invitrogen, Carlsbad, CA, USA) and peanut agglutinin (PNA; CL-1073-1; 1:500; Vector Labs, Burlingame, CA, USA) for 2 h at room temperature, after which the nuclei were counterstained with Hoechst 33342 (H3570; 1:5000; Invitrogen). .. Imaging was performed on a Zeiss LSM 980 confocal system (ZEISS, Oberkochen, Germany). mRNA expression analysis Total RNA was isolated from the peripheral blood of the NOA proband and OA control, after which first-strand complementary DNA (cDNA) synthesis was performed using a Takara PrimeScript RT Reagent Kit (6110A; Takara, Otsu, Japan) with random hexamers. .. Reverse transcription quantitative polymerase chain reaction (RT‒qPCR) was performed on a Bio-Rad CFX96 system with Takara TB Green Premix Ex Taq II (RR420A; Takara), with the following thermal cycling conditions: initial denaturation (95°C for 30 s), 40 cycles of 95°C for 5 s; and 60°C for 30 s. Relative BEND2 mRNA expressions were quantified via the 2−ΔCt method and normalized to that of glyceraldehyde-3phosphate dehydrogenase (GAPDH) using the following primers: BEND2 forward, 5’-CCAATTTGGAATCTGGCCCAC-3’, and BEND2 reverse, 5’-GGCCACTGTCACTGTCCAAT-3’; and GAPDH forward, 5’-GGAGCGAGATCCCTCCAAAAT-3’, and GAPDH reverse, 5’-GGCTGTTGTCATACTTCTCATGG-3’.

    Synthesized:

    Article Title: High Fat Diet‐Induced Obesity Alters Cutaneous Immune Cell Function, and These Changes Persist After Weight Loss
    Article Snippet: Total RNA was extracted from the tissues using ISOGEN (Nippon Gene CO. Ltd., Tokyo, Japan). .. Complementary deoxyribonucleic acid (cDNA) was synthesized using the PrimeScript 1st‐standard cDNA synthesis kit (TaKaRa Bio Inc., Otsu, Japan) according to the manufacturer’s instructions. .. Real‐time quantitative PCR was performed using gene‐specific primers and FastStart essential DNA green master mix (Sigma–Aldrich, St. Louis, MO, USA) on a StepOnePlus Real‐Time PCR System (Thermo Fisher Scientific, Inc., Waltham, USA).



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