Review



primescripttm one step rt pcr kit  (TaKaRa)


Bioz Verified Symbol TaKaRa is a verified supplier
Bioz Manufacturer Symbol TaKaRa manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 98

    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 10903 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+pcr+kit/PrimeScript+RT-PCR+Kit/pmc13195868-92-16-21
    Average 98 stars, based on 10903 article reviews
    primescripttm one step rt pcr kit - by Bioz Stars, 2026-09
    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 Polymerase Chain Reaction:

    Article Title: Therapeutic base editing alleviates restrictive cardiomyopathy
    Article Snippet: Uniclone One Step Seamless Cloning Kit , Genesand , SC612. .. PrimeScriptTM RT-PCR Kit , Takara , RR014A. .. TB Green® Premix Ex TaqTM (Tli RNaseH Plus) , Takara , Cat#RR420A.

    Article Title: Intelligent nanoliposome ameliorate chronic intermittent hypoxia-mediated neuronal injury via a dual regulation microglial inflammation strategy
    Article Snippet: Levels of IL-1β and TNF-α in supernatants were measured by ELISA kits (BioLegend) following the manufacturers’ instructions. .. Total RNA was isolated by Trizol reagent (10296028, Invitrogen), and complementary DNA was generated using the Takara RNA PCR kit (RR420A, Takara). qRT‐PCR was performed with PrimeScriptTM RT-PCR kit (RR036A, Takara) using the QuantStudio 3 Real-Time PCR Systems (Applied Biosystems). ..


    Article Title: Pathogenic mechanism of the PLS1 gene variant in hearing loss and functional validation in a zebrafish model.
    Article Snippet: Lentiviral overexpression vectors (Ubc-3FLAG-CBh-gcGFP-IRES-puromycin; PLS1-WT and PLS1-ΔExon8) were produced by GeneChem and transduced into HEK293T and HEI-OC1 (Pls1-KO) cells according to the manufacturer’s protocol. .. Puromycin selection was performed at 72 h post-transduction to establish stable cell lines. qRT-PCR Total RNA was extracted using an RNA extraction kit (Promega, Shanghai, China), according to the manufacturer’s protocol. cDNA synthesis was performed using the PrimeScriptTM RT-PCR Kit (Takara Bio, Japan). qRT-PCR was performed using the PrimeScript RT-PCR Kit (Takara, Japan). ..

    Article Title: DHT-Induced lncRNA AC092718.4 Promotes Prostate Cancer Cell Proliferation via ceRNA Mechanism
    Article Snippet: Total RNA was isolated using the RNeasy®Plus mini Kit (QIAGEN, Dusseldorf, Germany) according to the manufacturer’s protocol. .. Reverse transcription of total RNA was carried out using the PrimeScriptTM RT-PCR Kit (Takara, Tokyo, Japan), while reverse transcription of miRNAs was carried out with the miRNA 1st Strand cDNA Synthesis Kit (Vazyme, Nanjing, China). qPCR was conducted by using TB Green® Premix Ex TaqTM II (Tli RNaseH Plus) (Takara, Tokyo, Japan). ..

    Article Title: Inflammatory macrophage-derived plasminogen activator inhibitor-1 exacerbates inflammation through efferocytosis inhibition.
    Article Snippet: .. The RNA (0.5 μg) was reverse-transcribed to cDNA using the PrimeScriptTM RT-PCR kit (Takara Bio, Shiga, Japan), and gene expression levels were measured by qPCR analysis with TaqManTM Fast Advanced Master Mix and QuantStudioTM 3 Real Time PCR System (Thermo Fisher Scientific). .. Specific TaqMan TM primers/probes (Thermo Fisher Scientific) were used: mouse PAI-1 (Mm00435858_m1), TNF (Mm00443258_m1), IFN (Mm01168134_m1), IL-1 (Mm00434228_m1), IL-10 (Mm012883386_m1), CCL2 (Mm00441242_m1), AR TI CL E IN P RE SS and 18S RNA (Hs99999901_s1).

    Article Title: Multi-strategy engineering of Saccharomyces cerevisiae for enhanced β-ionone biosynthesis
    Article Snippet: β-Ionone is a natural volatile compound known for its distinctive violet and woody aroma, with broad application potential in the flavor, fragrance, and pharmaceutical industries.. To meet the growing market demand for natural products and overcome the limitations of chemical synthesis and plant extraction, microbial cell factories have emerged as a sustainable and environmentally friendly alternative.. In this study, a positive correlation was established between β-ionone production and the accumulation of its precursor, β-carotene.

    Isolation:

    Article Title: Intelligent nanoliposome ameliorate chronic intermittent hypoxia-mediated neuronal injury via a dual regulation microglial inflammation strategy
    Article Snippet: Levels of IL-1β and TNF-α in supernatants were measured by ELISA kits (BioLegend) following the manufacturers’ instructions. .. Total RNA was isolated by Trizol reagent (10296028, Invitrogen), and complementary DNA was generated using the Takara RNA PCR kit (RR420A, Takara). qRT‐PCR was performed with PrimeScriptTM RT-PCR kit (RR036A, Takara) using the QuantStudio 3 Real-Time PCR Systems (Applied Biosystems). ..

    Generated:

    Article Title: Intelligent nanoliposome ameliorate chronic intermittent hypoxia-mediated neuronal injury via a dual regulation microglial inflammation strategy
    Article Snippet: Levels of IL-1β and TNF-α in supernatants were measured by ELISA kits (BioLegend) following the manufacturers’ instructions. .. Total RNA was isolated by Trizol reagent (10296028, Invitrogen), and complementary DNA was generated using the Takara RNA PCR kit (RR420A, Takara). qRT‐PCR was performed with PrimeScriptTM RT-PCR kit (RR036A, Takara) using the QuantStudio 3 Real-Time PCR Systems (Applied Biosystems). ..

    Polymerase Chain Reaction:

    Article Title: Intelligent nanoliposome ameliorate chronic intermittent hypoxia-mediated neuronal injury via a dual regulation microglial inflammation strategy
    Article Snippet: Levels of IL-1β and TNF-α in supernatants were measured by ELISA kits (BioLegend) following the manufacturers’ instructions. .. Total RNA was isolated by Trizol reagent (10296028, Invitrogen), and complementary DNA was generated using the Takara RNA PCR kit (RR420A, Takara). qRT‐PCR was performed with PrimeScriptTM RT-PCR kit (RR036A, Takara) using the QuantStudio 3 Real-Time PCR Systems (Applied Biosystems). ..

    Real-time Polymerase Chain Reaction:

    Article Title: Intelligent nanoliposome ameliorate chronic intermittent hypoxia-mediated neuronal injury via a dual regulation microglial inflammation strategy
    Article Snippet: Levels of IL-1β and TNF-α in supernatants were measured by ELISA kits (BioLegend) following the manufacturers’ instructions. .. Total RNA was isolated by Trizol reagent (10296028, Invitrogen), and complementary DNA was generated using the Takara RNA PCR kit (RR420A, Takara). qRT‐PCR was performed with PrimeScriptTM RT-PCR kit (RR036A, Takara) using the QuantStudio 3 Real-Time PCR Systems (Applied Biosystems). ..

    Article Title: DHT-Induced lncRNA AC092718.4 Promotes Prostate Cancer Cell Proliferation via ceRNA Mechanism
    Article Snippet: Total RNA was isolated using the RNeasy®Plus mini Kit (QIAGEN, Dusseldorf, Germany) according to the manufacturer’s protocol. .. Reverse transcription of total RNA was carried out using the PrimeScriptTM RT-PCR Kit (Takara, Tokyo, Japan), while reverse transcription of miRNAs was carried out with the miRNA 1st Strand cDNA Synthesis Kit (Vazyme, Nanjing, China). qPCR was conducted by using TB Green® Premix Ex TaqTM II (Tli RNaseH Plus) (Takara, Tokyo, Japan). ..

    Article Title: Inflammatory macrophage-derived plasminogen activator inhibitor-1 exacerbates inflammation through efferocytosis inhibition.
    Article Snippet: .. The RNA (0.5 μg) was reverse-transcribed to cDNA using the PrimeScriptTM RT-PCR kit (Takara Bio, Shiga, Japan), and gene expression levels were measured by qPCR analysis with TaqManTM Fast Advanced Master Mix and QuantStudioTM 3 Real Time PCR System (Thermo Fisher Scientific). .. Specific TaqMan TM primers/probes (Thermo Fisher Scientific) were used: mouse PAI-1 (Mm00435858_m1), TNF (Mm00443258_m1), IFN (Mm01168134_m1), IL-1 (Mm00434228_m1), IL-10 (Mm012883386_m1), CCL2 (Mm00441242_m1), AR TI CL E IN P RE SS and 18S RNA (Hs99999901_s1).

    Article Title: Multi-strategy engineering of Saccharomyces cerevisiae for enhanced β-ionone biosynthesis
    Article Snippet: β-Ionone is a natural volatile compound known for its distinctive violet and woody aroma, with broad application potential in the flavor, fragrance, and pharmaceutical industries.. To meet the growing market demand for natural products and overcome the limitations of chemical synthesis and plant extraction, microbial cell factories have emerged as a sustainable and environmentally friendly alternative.. In this study, a positive correlation was established between β-ionone production and the accumulation of its precursor, β-carotene.

    Reverse Transcription:


    Article Title: DHT-Induced lncRNA AC092718.4 Promotes Prostate Cancer Cell Proliferation via ceRNA Mechanism
    Article Snippet: Total RNA was isolated using the RNeasy®Plus mini Kit (QIAGEN, Dusseldorf, Germany) according to the manufacturer’s protocol. .. Reverse transcription of total RNA was carried out using the PrimeScriptTM RT-PCR Kit (Takara, Tokyo, Japan), while reverse transcription of miRNAs was carried out with the miRNA 1st Strand cDNA Synthesis Kit (Vazyme, Nanjing, China). qPCR was conducted by using TB Green® Premix Ex TaqTM II (Tli RNaseH Plus) (Takara, Tokyo, Japan). ..

    Article Title: Inflammatory macrophage-derived plasminogen activator inhibitor-1 exacerbates inflammation through efferocytosis inhibition.
    Article Snippet: .. The RNA (0.5 μg) was reverse-transcribed to cDNA using the PrimeScriptTM RT-PCR kit (Takara Bio, Shiga, Japan), and gene expression levels were measured by qPCR analysis with TaqManTM Fast Advanced Master Mix and QuantStudioTM 3 Real Time PCR System (Thermo Fisher Scientific). .. Specific TaqMan TM primers/probes (Thermo Fisher Scientific) were used: mouse PAI-1 (Mm00435858_m1), TNF (Mm00443258_m1), IFN (Mm01168134_m1), IL-1 (Mm00434228_m1), IL-10 (Mm012883386_m1), CCL2 (Mm00441242_m1), AR TI CL E IN P RE SS and 18S RNA (Hs99999901_s1).

    Selection:

    Article Title: Pathogenic mechanism of the PLS1 gene variant in hearing loss and functional validation in a zebrafish model.
    Article Snippet: Lentiviral overexpression vectors (Ubc-3FLAG-CBh-gcGFP-IRES-puromycin; PLS1-WT and PLS1-ΔExon8) were produced by GeneChem and transduced into HEK293T and HEI-OC1 (Pls1-KO) cells according to the manufacturer’s protocol. .. Puromycin selection was performed at 72 h post-transduction to establish stable cell lines. qRT-PCR Total RNA was extracted using an RNA extraction kit (Promega, Shanghai, China), according to the manufacturer’s protocol. cDNA synthesis was performed using the PrimeScriptTM RT-PCR Kit (Takara Bio, Japan). qRT-PCR was performed using the PrimeScript RT-PCR Kit (Takara, Japan). ..

    Stable Transfection:

    Article Title: Pathogenic mechanism of the PLS1 gene variant in hearing loss and functional validation in a zebrafish model.
    Article Snippet: Lentiviral overexpression vectors (Ubc-3FLAG-CBh-gcGFP-IRES-puromycin; PLS1-WT and PLS1-ΔExon8) were produced by GeneChem and transduced into HEK293T and HEI-OC1 (Pls1-KO) cells according to the manufacturer’s protocol. .. Puromycin selection was performed at 72 h post-transduction to establish stable cell lines. qRT-PCR Total RNA was extracted using an RNA extraction kit (Promega, Shanghai, China), according to the manufacturer’s protocol. cDNA synthesis was performed using the PrimeScriptTM RT-PCR Kit (Takara Bio, Japan). qRT-PCR was performed using the PrimeScript RT-PCR Kit (Takara, Japan). ..

    Quantitative RT-PCR:

    Article Title: Pathogenic mechanism of the PLS1 gene variant in hearing loss and functional validation in a zebrafish model.
    Article Snippet: Lentiviral overexpression vectors (Ubc-3FLAG-CBh-gcGFP-IRES-puromycin; PLS1-WT and PLS1-ΔExon8) were produced by GeneChem and transduced into HEK293T and HEI-OC1 (Pls1-KO) cells according to the manufacturer’s protocol. .. Puromycin selection was performed at 72 h post-transduction to establish stable cell lines. qRT-PCR Total RNA was extracted using an RNA extraction kit (Promega, Shanghai, China), according to the manufacturer’s protocol. cDNA synthesis was performed using the PrimeScriptTM RT-PCR Kit (Takara Bio, Japan). qRT-PCR was performed using the PrimeScript RT-PCR Kit (Takara, Japan). ..

    Article Title: Multi-strategy engineering of Saccharomyces cerevisiae for enhanced β-ionone biosynthesis
    Article Snippet: β-Ionone is a natural volatile compound known for its distinctive violet and woody aroma, with broad application potential in the flavor, fragrance, and pharmaceutical industries.. To meet the growing market demand for natural products and overcome the limitations of chemical synthesis and plant extraction, microbial cell factories have emerged as a sustainable and environmentally friendly alternative.. In this study, a positive correlation was established between β-ionone production and the accumulation of its precursor, β-carotene.

    RNA Extraction:

    Article Title: Pathogenic mechanism of the PLS1 gene variant in hearing loss and functional validation in a zebrafish model.
    Article Snippet: Lentiviral overexpression vectors (Ubc-3FLAG-CBh-gcGFP-IRES-puromycin; PLS1-WT and PLS1-ΔExon8) were produced by GeneChem and transduced into HEK293T and HEI-OC1 (Pls1-KO) cells according to the manufacturer’s protocol. .. Puromycin selection was performed at 72 h post-transduction to establish stable cell lines. qRT-PCR Total RNA was extracted using an RNA extraction kit (Promega, Shanghai, China), according to the manufacturer’s protocol. cDNA synthesis was performed using the PrimeScriptTM RT-PCR Kit (Takara Bio, Japan). qRT-PCR was performed using the PrimeScript RT-PCR Kit (Takara, Japan). ..

    cDNA Synthesis:

    Article Title: Pathogenic mechanism of the PLS1 gene variant in hearing loss and functional validation in a zebrafish model.
    Article Snippet: Lentiviral overexpression vectors (Ubc-3FLAG-CBh-gcGFP-IRES-puromycin; PLS1-WT and PLS1-ΔExon8) were produced by GeneChem and transduced into HEK293T and HEI-OC1 (Pls1-KO) cells according to the manufacturer’s protocol. .. Puromycin selection was performed at 72 h post-transduction to establish stable cell lines. qRT-PCR Total RNA was extracted using an RNA extraction kit (Promega, Shanghai, China), according to the manufacturer’s protocol. cDNA synthesis was performed using the PrimeScriptTM RT-PCR Kit (Takara Bio, Japan). qRT-PCR was performed using the PrimeScript RT-PCR Kit (Takara, Japan). ..

    Article Title: DHT-Induced lncRNA AC092718.4 Promotes Prostate Cancer Cell Proliferation via ceRNA Mechanism
    Article Snippet: Total RNA was isolated using the RNeasy®Plus mini Kit (QIAGEN, Dusseldorf, Germany) according to the manufacturer’s protocol. .. Reverse transcription of total RNA was carried out using the PrimeScriptTM RT-PCR Kit (Takara, Tokyo, Japan), while reverse transcription of miRNAs was carried out with the miRNA 1st Strand cDNA Synthesis Kit (Vazyme, Nanjing, China). qPCR was conducted by using TB Green® Premix Ex TaqTM II (Tli RNaseH Plus) (Takara, Tokyo, Japan). ..

    Article Title: Red light pretreatment promotes esters biosynthesis by activating the CmBBX7/14-CmLOX18-CmAAT1 module in postharvest oriental melon at low temperature
    Article Snippet: Combining light quality regulation with postharvest low-temperature storage holds promise for mitigating postharvest aroma loss in fruits.. However, the molecular mechanism by which light quality modulates postharvest aroma biosynthesis remains unclear.. In this study, ‘Bali Xiang’ oriental melon fruit at the early stage of ethylene release were selected as experimental material and subjected to red light (RLT) or blue light (BLT) pretreatment prior to low-temperature storage.

    Gene Expression:

    Article Title: Inflammatory macrophage-derived plasminogen activator inhibitor-1 exacerbates inflammation through efferocytosis inhibition.
    Article Snippet: .. The RNA (0.5 μg) was reverse-transcribed to cDNA using the PrimeScriptTM RT-PCR kit (Takara Bio, Shiga, Japan), and gene expression levels were measured by qPCR analysis with TaqManTM Fast Advanced Master Mix and QuantStudioTM 3 Real Time PCR System (Thermo Fisher Scientific). .. Specific TaqMan TM primers/probes (Thermo Fisher Scientific) were used: mouse PAI-1 (Mm00435858_m1), TNF (Mm00443258_m1), IFN (Mm01168134_m1), IL-1 (Mm00434228_m1), IL-10 (Mm012883386_m1), CCL2 (Mm00441242_m1), AR TI CL E IN P RE SS and 18S RNA (Hs99999901_s1).



    Similar Products

    98
    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 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+pcr+kit/PrimeScript+RT-PCR+Kit/pmc13195868-92-16-21
    Average 98 stars, based on 1 article reviews
    primescripttm one step rt pcr kit - by Bioz Stars, 2026-09
    98/100 stars
      Buy from Supplier

    97
    TaKaRa one step sybr primescripttm 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.
    One Step Sybr Primescripttm Rt Pcr Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+pcr+kit/One+Step+PrimeScript+RT-PCR+Kit/pm42134762-109-6-14
    Average 97 stars, based on 1 article reviews
    one step sybr primescripttm rt pcr kit - by Bioz Stars, 2026-09
    97/100 stars
      Buy from Supplier

    98
    TaKaRa primescripttm rt 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 Rt Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 98/100, based on 1 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 1 article reviews
    primescripttm rt kit - by Bioz Stars, 2026-09
    98/100 stars
      Buy from Supplier

    98
    TaKaRa primescripttm 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 Rt Pcr Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+pcr+kit/PrimeScript+RT-PCR+Kit/10__3390_slash_genes17050538-93-10-13
    Average 98 stars, based on 1 article reviews
    primescripttm rt pcr kit - by Bioz Stars, 2026-09
    98/100 stars
      Buy from Supplier

    97
    TaKaRa one step primescripttm 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.
    One Step Primescripttm Rt Pcr Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+pcr+kit/One+Step+PrimeScript+RT-PCR+Kit/pmc13128697-57-7-15
    Average 97 stars, based on 1 article reviews
    one step primescripttm rt pcr kit - by Bioz Stars, 2026-09
    97/100 stars
      Buy from Supplier

    95
    TaKaRa primescripttm ii high fidelity 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 Ii High Fidelity One Step Rt Pcr Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+pcr+kit/High+Fidelity+one-step+RT-PCR/pm42056564-62-12-19
    Average 95 stars, based on 1 article reviews
    primescripttm ii high fidelity one step rt pcr kit - by Bioz Stars, 2026-09
    95/100 stars
      Buy from Supplier

    96
    TaKaRa primescripttm ii high fidelity 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 Ii High Fidelity Rt Pcr Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+pcr+kit/PrimeScript+High+Fidelity+RT-PCR+Kit/pmc13167943-53-4-11
    Average 96 stars, based on 1 article reviews
    primescripttm ii high fidelity rt pcr kit - by Bioz Stars, 2026-09
    96/100 stars
      Buy from Supplier

    96
    TaKaRa primescripttm rt qpcr 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 Rt Qpcr Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+pcr+kit/One-Step+TB+Green+PrimeScript+RT-PCR+Kit+II/pmc13104215-77-7-11
    Average 96 stars, based on 1 article reviews
    primescripttm rt qpcr kit - by Bioz Stars, 2026-09
    96/100 stars
      Buy from Supplier

    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