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primescripttm rt kit  (TaKaRa)


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    Structured Review

    TaKaRa primescripttm rt kit
    Primescripttm Rt Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 98/100, based on 10983 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+pcr+kit/PrimeScript+RT-PCR+Kit/pm42116160-176-15-18
    Average 98 stars, based on 10983 article reviews
    primescripttm rt kit - by Bioz Stars, 2026-10
    98/100 stars

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    Related Articles

    Reverse Transcription:

    Article Title: A core transcriptional regulatory circuitry controls super-enhancer-driven activation of LGR5 in colorectal cancer.
    Article Snippet: Total RNA was extracted by TRIzol reagent (Life Technologies) according to the manufacturer’s instructions. .. One microgram of RNA was used for each reverse transcription reaction, which was set by PrimeScript RT kit with genomic DNA eraser (Takara). .. qRT-PCR was conducted using SYBR Green PCR Master Mix (Takara) on a qTOWER platform (Jena).

    Article Title: Dichloroacetate mitigates experimental abdominal aortic aneurysm via suppression of CXCL5-mediated neutrophil chemotaxis.
    Article Snippet: Background: Abdominal aortic aneurysm (AAA) is a life-threatening vascular disease with high rupture-associated mortality.. Current management relies on surgical or endovascular repair, with no effective pharmacological therapy.. Inflammation and immune cell infiltration are central to AAA pathogenesis, but the molecular mechanisms remain incompletely defined.

    Article Title: Decitabine induces cell differentiation and growth inhibition accompanied by upregulation of microRNA-143 and MS4A3 in the myelodysplastic syndromes-derived leukemic cell line MDS-L.
    Article Snippet: RNA was extracted from cells using a RNeasy Mini Kit (Qiagen Sciences, Inc.). .. Total RNA was reverse transcribed to cDNA using a PrimeScript RT‐PCR kit (Takara Bio, Inc.) and TaqMan MicroRNA Reverse Transcription kit (cat. no. 4366597; Thermo Fisher Scientific, Inc.). .. Quantitative PCR was carried out using a TaqMan Fast Advanced Master Mix kit and Step One Plus real‐time PCR systems (Applied Biosystems; Thermo Fisher Scientific, Inc.) with the following conditions: An initial 95 ̊C for 20 sec, followed by 40 cycles of 95 ̊C for 1 sec and 60 ̊C for 20 sec.

    Article Title: Visualizing intestinal colonization of GFP-displayed Lactobacillus plantarum PO23 and its effects on intestinal morphology and immunity in Paralichthys olivaceus.
    Article Snippet: Visualization of probiotic intestinal colonization is essential for clarifying their adhesion characteristics and mucosal immunomodulatory mechanisms.. GFP surface display enables real-time visualization of probiotic attachment, distribution, and migration dynamics in living hosts.. In our previous study, a highly adhesive potential probiotic strain, Lactobacillus plantarum PO23 (LP-PO23), was isolated from the intestine of flounder (Paralichthys olivaceus).

    cDNA Synthesis:

    Article Title: β-Thujaplicin modulates the ODC-ROS-linked apoptosis in H460 lung cancer cells.
    Article Snippet: This study explored the antiproliferative effects of β-thujaplicin, a natural tropolone derivative, in the non-small-cell lung cancer (NSCLC) cell lines H460 and A549 and in L132 normal lung epithelial cells, using MTT, NRU, and SRB assays.. β-Thujaplicin exhibited concentration-dependent cytotoxicity in H460 and A549 cells but had minimal effect on L132 cells.. Mechanistic studies in H460 cells showed suppression of ornithine decarboxylase (ODC) activity and ODC mRNA expression, along with alterations in polyamine metabolite abundance detected by LC-HRMS.

    SYBR Green Assay:

    Article Title: β-Thujaplicin modulates the ODC-ROS-linked apoptosis in H460 lung cancer cells.
    Article Snippet: This study explored the antiproliferative effects of β-thujaplicin, a natural tropolone derivative, in the non-small-cell lung cancer (NSCLC) cell lines H460 and A549 and in L132 normal lung epithelial cells, using MTT, NRU, and SRB assays.. β-Thujaplicin exhibited concentration-dependent cytotoxicity in H460 and A549 cells but had minimal effect on L132 cells.. Mechanistic studies in H460 cells showed suppression of ornithine decarboxylase (ODC) activity and ODC mRNA expression, along with alterations in polyamine metabolite abundance detected by LC-HRMS.

    Polymerase Chain Reaction:

    Article Title: β-Thujaplicin modulates the ODC-ROS-linked apoptosis in H460 lung cancer cells.
    Article Snippet: This study explored the antiproliferative effects of β-thujaplicin, a natural tropolone derivative, in the non-small-cell lung cancer (NSCLC) cell lines H460 and A549 and in L132 normal lung epithelial cells, using MTT, NRU, and SRB assays.. β-Thujaplicin exhibited concentration-dependent cytotoxicity in H460 and A549 cells but had minimal effect on L132 cells.. Mechanistic studies in H460 cells showed suppression of ornithine decarboxylase (ODC) activity and ODC mRNA expression, along with alterations in polyamine metabolite abundance detected by LC-HRMS.

    Reverse Transcription Polymerase Chain Reaction:

    Article Title: The capsid proteins of orthoflavivirus are interchangeable for West Nile virus assembly.
    Article Snippet: .. Total RNAs of WNV-DV2mC-P10-A/B/C-infected cells were extracted, and RT-PCR was then carried out using the PrimeScript One Step RT-PCR Kit (Takara) with primers to amplify the fragments spanning from 5′ UTR to 3′ UTR. ..

    Article Title: Dichloroacetate mitigates experimental abdominal aortic aneurysm via suppression of CXCL5-mediated neutrophil chemotaxis.
    Article Snippet: Background: Abdominal aortic aneurysm (AAA) is a life-threatening vascular disease with high rupture-associated mortality.. Current management relies on surgical or endovascular repair, with no effective pharmacological therapy.. Inflammation and immune cell infiltration are central to AAA pathogenesis, but the molecular mechanisms remain incompletely defined.

    Article Title: Visualizing intestinal colonization of GFP-displayed Lactobacillus plantarum PO23 and its effects on intestinal morphology and immunity in Paralichthys olivaceus.
    Article Snippet: Visualization of probiotic intestinal colonization is essential for clarifying their adhesion characteristics and mucosal immunomodulatory mechanisms.. GFP surface display enables real-time visualization of probiotic attachment, distribution, and migration dynamics in living hosts.. In our previous study, a highly adhesive potential probiotic strain, Lactobacillus plantarum PO23 (LP-PO23), was isolated from the intestine of flounder (Paralichthys olivaceus).

    Article Title: Integrated in vivo and transcriptomic analyses of lethal Oropouche virus infection reveal suppression of pathogenic host responses by antiviral therapy
    Article Snippet: .. Measurements of host gene expression were performed using One Step TB Green PrimeScript RT-PCR Kit II (Perfect Real Time) (Takara). ..

    Article Title: Dual role of melatonin on Fusarium graminearum in vitro growth and on wheat seedlings infection
    Article Snippet: .. For each sample, according to the manufacturer’s protocols, total RNA was extracted from 100 mg of FG8 mycelium or wheat seedlings using the PureLink RNA Mini Kit (Ambion, Life Technologies, Carlsbad, CA, USA), DNase treatment was performed using the PureLink DNase Set (Ambion, Life Technologies), total RNA concentration was measured using a NanoDrop One (Thermo Fisher Scientific) spectrophotometer and the corresponding single strand cDNA was synthesized from 500 ng of total RNA using PrimeScript RT-PCR Kit (Takara Bio Inc.). .. The Reverse Transcription quantitative PCR (RT-qPCR) was carried out in the CFX Opus 96 Real-Time PCR System (Bio-Rad), using the SYBR Premix Ex Taq II reagent kit (Takara Bio Inc.), according to the manufacturer’s protocols.

    One Step RT-PCR:

    Article Title: The capsid proteins of orthoflavivirus are interchangeable for West Nile virus assembly.
    Article Snippet: .. Total RNAs of WNV-DV2mC-P10-A/B/C-infected cells were extracted, and RT-PCR was then carried out using the PrimeScript One Step RT-PCR Kit (Takara) with primers to amplify the fragments spanning from 5′ UTR to 3′ UTR. ..

    Real-time Polymerase Chain Reaction:

    Article Title: Dichloroacetate mitigates experimental abdominal aortic aneurysm via suppression of CXCL5-mediated neutrophil chemotaxis.
    Article Snippet: Background: Abdominal aortic aneurysm (AAA) is a life-threatening vascular disease with high rupture-associated mortality.. Current management relies on surgical or endovascular repair, with no effective pharmacological therapy.. Inflammation and immune cell infiltration are central to AAA pathogenesis, but the molecular mechanisms remain incompletely defined.

    Gene Expression:

    Article Title: Integrated in vivo and transcriptomic analyses of lethal Oropouche virus infection reveal suppression of pathogenic host responses by antiviral therapy
    Article Snippet: .. Measurements of host gene expression were performed using One Step TB Green PrimeScript RT-PCR Kit II (Perfect Real Time) (Takara). ..

    Concentration Assay:

    Article Title: Dual role of melatonin on Fusarium graminearum in vitro growth and on wheat seedlings infection
    Article Snippet: .. For each sample, according to the manufacturer’s protocols, total RNA was extracted from 100 mg of FG8 mycelium or wheat seedlings using the PureLink RNA Mini Kit (Ambion, Life Technologies, Carlsbad, CA, USA), DNase treatment was performed using the PureLink DNase Set (Ambion, Life Technologies), total RNA concentration was measured using a NanoDrop One (Thermo Fisher Scientific) spectrophotometer and the corresponding single strand cDNA was synthesized from 500 ng of total RNA using PrimeScript RT-PCR Kit (Takara Bio Inc.). .. The Reverse Transcription quantitative PCR (RT-qPCR) was carried out in the CFX Opus 96 Real-Time PCR System (Bio-Rad), using the SYBR Premix Ex Taq II reagent kit (Takara Bio Inc.), according to the manufacturer’s protocols.

    Spectrophotometry:

    Article Title: Dual role of melatonin on Fusarium graminearum in vitro growth and on wheat seedlings infection
    Article Snippet: .. For each sample, according to the manufacturer’s protocols, total RNA was extracted from 100 mg of FG8 mycelium or wheat seedlings using the PureLink RNA Mini Kit (Ambion, Life Technologies, Carlsbad, CA, USA), DNase treatment was performed using the PureLink DNase Set (Ambion, Life Technologies), total RNA concentration was measured using a NanoDrop One (Thermo Fisher Scientific) spectrophotometer and the corresponding single strand cDNA was synthesized from 500 ng of total RNA using PrimeScript RT-PCR Kit (Takara Bio Inc.). .. The Reverse Transcription quantitative PCR (RT-qPCR) was carried out in the CFX Opus 96 Real-Time PCR System (Bio-Rad), using the SYBR Premix Ex Taq II reagent kit (Takara Bio Inc.), according to the manufacturer’s protocols.

    Synthesized:

    Article Title: Dual role of melatonin on Fusarium graminearum in vitro growth and on wheat seedlings infection
    Article Snippet: .. For each sample, according to the manufacturer’s protocols, total RNA was extracted from 100 mg of FG8 mycelium or wheat seedlings using the PureLink RNA Mini Kit (Ambion, Life Technologies, Carlsbad, CA, USA), DNase treatment was performed using the PureLink DNase Set (Ambion, Life Technologies), total RNA concentration was measured using a NanoDrop One (Thermo Fisher Scientific) spectrophotometer and the corresponding single strand cDNA was synthesized from 500 ng of total RNA using PrimeScript RT-PCR Kit (Takara Bio Inc.). .. The Reverse Transcription quantitative PCR (RT-qPCR) was carried out in the CFX Opus 96 Real-Time PCR System (Bio-Rad), using the SYBR Premix Ex Taq II reagent kit (Takara Bio Inc.), according to the manufacturer’s protocols.



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    Construction and screening of phage display library . A PBMCs were isolated from camels, and RNA was extracted as a template <t>for</t> <t>RT-PCR</t> to amplify the gene sequence containing the leader signal sequence before the CH2 region. The amplification yielded two fragments: a 900-bp fragment (VH–CH1–CH2) and a 600-bp fragment (VHH–CH2). Lane M represents the DNA marker (2000–100 bp), and lanes 1–4 represent the amplified fragments. B The 600-bp fragment obtained from the first round of PCR was used as a template for the second round of PCR, which successfully generated the full-length VHH gene (spanning FR1 to FR4) with an approximate size of 400 bp. Lane M represents the DNA marker (1000–200 bp), and lanes 1–4 represent the amplified fragments. C A total of 16 clones were randomly selected from the constructed phage antibody library for identification. D Overall, 92 recombinant phage clones were randomly selected from the third round of panning and added to microplates coated with BRV. HRP-conjugated anti-M13 monoclonal antibody was used to detect the bound phages. M13K07 helper phage and PBS served as the negative control and blank control, respectively. Positive clones were defined as those with a sample-to-negative control ratio (P/N) ≥ 2.1, i.e., clones above the reference line were identified as positive.
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    Construction and screening of phage display library . A PBMCs were isolated from camels, and RNA was extracted as a template <t>for</t> <t>RT-PCR</t> to amplify the gene sequence containing the leader signal sequence before the CH2 region. The amplification yielded two fragments: a 900-bp fragment (VH–CH1–CH2) and a 600-bp fragment (VHH–CH2). Lane M represents the DNA marker (2000–100 bp), and lanes 1–4 represent the amplified fragments. B The 600-bp fragment obtained from the first round of PCR was used as a template for the second round of PCR, which successfully generated the full-length VHH gene (spanning FR1 to FR4) with an approximate size of 400 bp. Lane M represents the DNA marker (1000–200 bp), and lanes 1–4 represent the amplified fragments. C A total of 16 clones were randomly selected from the constructed phage antibody library for identification. D Overall, 92 recombinant phage clones were randomly selected from the third round of panning and added to microplates coated with BRV. HRP-conjugated anti-M13 monoclonal antibody was used to detect the bound phages. M13K07 helper phage and PBS served as the negative control and blank control, respectively. Positive clones were defined as those with a sample-to-negative control ratio (P/N) ≥ 2.1, i.e., clones above the reference line were identified as positive.
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    Image Search Results


    Construction and screening of phage display library . A PBMCs were isolated from camels, and RNA was extracted as a template for RT-PCR to amplify the gene sequence containing the leader signal sequence before the CH2 region. The amplification yielded two fragments: a 900-bp fragment (VH–CH1–CH2) and a 600-bp fragment (VHH–CH2). Lane M represents the DNA marker (2000–100 bp), and lanes 1–4 represent the amplified fragments. B The 600-bp fragment obtained from the first round of PCR was used as a template for the second round of PCR, which successfully generated the full-length VHH gene (spanning FR1 to FR4) with an approximate size of 400 bp. Lane M represents the DNA marker (1000–200 bp), and lanes 1–4 represent the amplified fragments. C A total of 16 clones were randomly selected from the constructed phage antibody library for identification. D Overall, 92 recombinant phage clones were randomly selected from the third round of panning and added to microplates coated with BRV. HRP-conjugated anti-M13 monoclonal antibody was used to detect the bound phages. M13K07 helper phage and PBS served as the negative control and blank control, respectively. Positive clones were defined as those with a sample-to-negative control ratio (P/N) ≥ 2.1, i.e., clones above the reference line were identified as positive.

    Journal: Veterinary Research

    Article Title: Potent neutralization and therapeutic efficacy of bovine rotavirus-specific VHH antibodies in infected calves

    doi: 10.1186/s13567-026-01765-3

    Figure Lengend Snippet: Construction and screening of phage display library . A PBMCs were isolated from camels, and RNA was extracted as a template for RT-PCR to amplify the gene sequence containing the leader signal sequence before the CH2 region. The amplification yielded two fragments: a 900-bp fragment (VH–CH1–CH2) and a 600-bp fragment (VHH–CH2). Lane M represents the DNA marker (2000–100 bp), and lanes 1–4 represent the amplified fragments. B The 600-bp fragment obtained from the first round of PCR was used as a template for the second round of PCR, which successfully generated the full-length VHH gene (spanning FR1 to FR4) with an approximate size of 400 bp. Lane M represents the DNA marker (1000–200 bp), and lanes 1–4 represent the amplified fragments. C A total of 16 clones were randomly selected from the constructed phage antibody library for identification. D Overall, 92 recombinant phage clones were randomly selected from the third round of panning and added to microplates coated with BRV. HRP-conjugated anti-M13 monoclonal antibody was used to detect the bound phages. M13K07 helper phage and PBS served as the negative control and blank control, respectively. Positive clones were defined as those with a sample-to-negative control ratio (P/N) ≥ 2.1, i.e., clones above the reference line were identified as positive.

    Article Snippet: The extracted RNA was directly subjected to one-step reverse-transcription polymerase chain reaction (RT-PCR) amplification using the PrimeScriptTM One Step RT-PCR Kit (TaKaRa, Shiga, Japan), which allows reverse transcription and PCR amplification to be conducted in a single reaction.

    Techniques: Isolation, Reverse Transcription Polymerase Chain Reaction, Sequencing, Amplification, Marker, Generated, Clone Assay, Construct, Recombinant, Negative Control, Control