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primescripttm one step rt pcr kit  (TaKaRa)


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    Structured Review

    TaKaRa primescripttm one step rt pcr kit
    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.
    Primescripttm One Step Rt Pcr Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 98/100, based on 10947 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/step+primescript+rt+pcr+kit/PrimeScript+RT-PCR+Kit/pmc13195868-92-16-21
    Average 98 stars, based on 10947 article reviews
    primescripttm one step rt pcr kit - by Bioz Stars, 2026-10
    98/100 stars

    Images

    1) Product Images from "Potent neutralization and therapeutic efficacy of bovine rotavirus-specific VHH antibodies in infected calves"

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

    Journal: Veterinary Research

    doi: 10.1186/s13567-026-01765-3

    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.
    Figure Legend 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.

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

    Related Articles

    Reverse Transcription:

    Article Title: KRAS (G12D)-selective inhibitor MRTX1133 suppresses proliferation and differentially modulates chemosensitivity in ovarian mucinous carcinoma
    Article Snippet: Cellular mRNA was extracted using the RNeasy Mini Kit (Qiagen, Inc.) according to the manufacturer's instructions. .. Reverse transcription and subsequent qPCR were performed using the One Step TB Green PrimeScript RT-PCR Kit II (Perfect Real Time; cat. no. RR066A; Takara Bio, Inc.), which includes TB Green as the fluorophore, according to the manufacturer's protocol. .. RT-qPCR was performed using the Thermal Cycler Dice Real Time System II (Takara Bio, Inc.) following the manufacturer's instructions.

    Article Title: Mettl3-modified lncRNA Snhg16 aggravates osteoarthritis via promoting chondrocyte ferroptosis by regulating Snd1/Gpx4 axis.
    Article Snippet: Purpose/Aim: Long noncoding RNA (lncRNA) small nucleolar RNA host gene 16 (Snhg16) has been confirmed to accelerate osteoarthritis (OA) progress.. However, its regulatory mechanism has not been fully elucidated.. Materials and Methods: Interleukin-1β (IL-1β)-induced ATDC5 chondrocytes were used to mimic OA cell models, and destabilization of medial meniscus (DMM) surgery was performed to construct OA mice models.

    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: Establishment and preliminary evaluation of an RT-ERA combined with CRISPR/Cas12a assay for detection of H5 and H7 influenza viruses
    Article Snippet: .. RT-qPCR was performed using the 2×One Step PrimeScript RT-PCR Kit (Takara) with the following conditions: reverse transcription at 42 °C for 5 min, initial denaturation at 95 °C for 10 s, followed by 40 cycles of 95 °C for 5 s and 60 °C for 34 s. Fluorescence signals were acquired at the 60 °C annealing-extension step. ..

    Real-time Polymerase Chain Reaction:

    Article Title: KRAS (G12D)-selective inhibitor MRTX1133 suppresses proliferation and differentially modulates chemosensitivity in ovarian mucinous carcinoma
    Article Snippet: Cellular mRNA was extracted using the RNeasy Mini Kit (Qiagen, Inc.) according to the manufacturer's instructions. .. Reverse transcription and subsequent qPCR were performed using the One Step TB Green PrimeScript RT-PCR Kit II (Perfect Real Time; cat. no. RR066A; Takara Bio, Inc.), which includes TB Green as the fluorophore, according to the manufacturer's protocol. .. RT-qPCR was performed using the Thermal Cycler Dice Real Time System II (Takara Bio, Inc.) following the manufacturer's instructions.

    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.

    Reverse Transcription Polymerase Chain Reaction:

    Article Title: KRAS (G12D)-selective inhibitor MRTX1133 suppresses proliferation and differentially modulates chemosensitivity in ovarian mucinous carcinoma
    Article Snippet: Cellular mRNA was extracted using the RNeasy Mini Kit (Qiagen, Inc.) according to the manufacturer's instructions. .. Reverse transcription and subsequent qPCR were performed using the One Step TB Green PrimeScript RT-PCR Kit II (Perfect Real Time; cat. no. RR066A; Takara Bio, Inc.), which includes TB Green as the fluorophore, according to the manufacturer's protocol. .. RT-qPCR was performed using the Thermal Cycler Dice Real Time System II (Takara Bio, Inc.) following the manufacturer's instructions.

    Article Title: Mettl3-modified lncRNA Snhg16 aggravates osteoarthritis via promoting chondrocyte ferroptosis by regulating Snd1/Gpx4 axis.
    Article Snippet: Purpose/Aim: Long noncoding RNA (lncRNA) small nucleolar RNA host gene 16 (Snhg16) has been confirmed to accelerate osteoarthritis (OA) progress.. However, its regulatory mechanism has not been fully elucidated.. Materials and Methods: Interleukin-1β (IL-1β)-induced ATDC5 chondrocytes were used to mimic OA cell models, and destabilization of medial meniscus (DMM) surgery was performed to construct OA mice models.

    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: Establishment and preliminary evaluation of an RT-ERA combined with CRISPR/Cas12a assay for detection of H5 and H7 influenza viruses
    Article Snippet: .. RT-qPCR was performed using the 2×One Step PrimeScript RT-PCR Kit (Takara) with the following conditions: reverse transcription at 42 °C for 5 min, initial denaturation at 95 °C for 10 s, followed by 40 cycles of 95 °C for 5 s and 60 °C for 34 s. Fluorescence signals were acquired at the 60 °C annealing-extension step. ..

    Article Title: Exercise suppresses IP6K3 to modulate BCAA metabolism and ferroptosis in MASLD
    Article Snippet: For quantitative PCR analysis, total RNA was extracted using RNAiso Extract Reagent (Takara, Japan). .. The PCR reaction was performed with a two-step SYBR PrimeScript RT-PCR Kit (Takara, Japan) in a CFX96 system (Bio-Rad) using specific primers. ..

    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.

    Article Title: Exercise suppresses IP6K3 to modulate BCAA metabolism and ferroptosis in MASLD
    Article Snippet: For quantitative PCR analysis, total RNA was extracted using RNAiso Extract Reagent (Takara, Japan). .. The PCR reaction was performed with a two-step SYBR PrimeScript RT-PCR Kit (Takara, Japan) in a CFX96 system (Bio-Rad) using specific primers. ..

    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. ..

    Quantitative RT-PCR:

    Article Title: Establishment and preliminary evaluation of an RT-ERA combined with CRISPR/Cas12a assay for detection of H5 and H7 influenza viruses
    Article Snippet: .. RT-qPCR was performed using the 2×One Step PrimeScript RT-PCR Kit (Takara) with the following conditions: reverse transcription at 42 °C for 5 min, initial denaturation at 95 °C for 10 s, followed by 40 cycles of 95 °C for 5 s and 60 °C for 34 s. Fluorescence signals were acquired at the 60 °C annealing-extension step. ..

    Fluorescence:

    Article Title: Establishment and preliminary evaluation of an RT-ERA combined with CRISPR/Cas12a assay for detection of H5 and H7 influenza viruses
    Article Snippet: .. RT-qPCR was performed using the 2×One Step PrimeScript RT-PCR Kit (Takara) with the following conditions: reverse transcription at 42 °C for 5 min, initial denaturation at 95 °C for 10 s, followed by 40 cycles of 95 °C for 5 s and 60 °C for 34 s. Fluorescence signals were acquired at the 60 °C annealing-extension step. ..



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