Review



one step tb green primescript rt pcr kit ii  (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 one step tb green primescript rt pcr kit ii
    One Step Tb Green Primescript Rt Pcr Kit Ii, supplied by TaKaRa, used in various techniques. Bioz Stars score: 98/100, based on 10933 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/pmc13107096-64-9-23
    Average 98 stars, based on 10933 article reviews
    one step tb green primescript rt pcr kit ii - by Bioz Stars, 2026-10
    98/100 stars

    Images

    Related Articles

    Quantitative RT-PCR:

    Article Title: Inhibition of Farnesoid-x-receptor signaling during abdominal sepsis by dysbiosis exacerbates gut barrier dysfunction.
    Article Snippet: To determine relative gene expression in the ileum, RNA was isolated by using TRIZOL (Invitrogen, Carlsbard, CA, USA) following the manufacturer’s instructions, and quantified by a NanoDrop1000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA). cDNA was processed with the cDNA synthesis kit (Thermo Fisher Scientific, Waltham, MA, USA) according to the standard protocol. .. RT-qPCR was conducted on the QuantStudioTM 7 Flex System using one step PrimeScript® RT-PCR Kit (Takara, RR064 A, Tokyo, Japan). ..

    Article Title: NLRP3 Inflammasome Activation Mediates Hepatitis E Virus-Induced Neuroinflammation.
    Article Snippet: Hepatitis E virus (HEV) is a foodborne zoonotic pathogen that is supposed to be one of the most common causes of acute viral hepatitis.. However, HEV infection has been recently associated with a wide spectrum of extrahepatic manifestations, particularly neurological disorders.. Previous studies have shown that HEV is able to cross the blood–brain barrier (BBB) and induce inflammatory response of the central nervous system.

    Article Title: Inhibition of Farnesoid-x-receptor signaling during abdominal sepsis by dysbiosis exacerbates gut barrier dysfunction
    Article Snippet: To determine relative gene expression in the ileum, RNA was isolated by using TRIZOL (Invitrogen, Carlsbard, CA, USA) following the manufacturer’s instructions, and quantified by a NanoDrop1000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA). cDNA was processed with the cDNA synthesis kit (Thermo Fisher Scientific, Waltham, MA, USA) according to the standard protocol. .. RT-qPCR was conducted on the QuantStudioTM 7 Flex System using one step PrimeScript® RT-PCR Kit (Takara, RR064 A, Tokyo, Japan). ..

    Article Title: HSF1–DBC1 axis drives prostate cancer progression by activating a metastatic transcriptional program
    Article Snippet: .. Real-time quantitative reverse transcription-PCR (qRT-PCR) Total RNA was extracted using TRIzol reagent (Invitrogen), and qRT-PCR was performed using the One- step PrimeScript RT-PCR Kit (Takara Bio). qRT-PCR was performed in triplicate using gene-specific primers on QuantStudio 6 Flex real-time PCR system (Applied Biosystems). ..

    Article Title: Characterization of the virus-host RNA-RNA interactome across important human pathogenic RNA viruses.
    Article Snippet: .. SYBR Green RT-qPCR was performed using the One step primescript RT-PCR kit (Takara) according to manufacturer’s instructions. ..

    Reverse Transcription Polymerase Chain Reaction:

    Article Title: Inhibition of Farnesoid-x-receptor signaling during abdominal sepsis by dysbiosis exacerbates gut barrier dysfunction.
    Article Snippet: To determine relative gene expression in the ileum, RNA was isolated by using TRIZOL (Invitrogen, Carlsbard, CA, USA) following the manufacturer’s instructions, and quantified by a NanoDrop1000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA). cDNA was processed with the cDNA synthesis kit (Thermo Fisher Scientific, Waltham, MA, USA) according to the standard protocol. .. RT-qPCR was conducted on the QuantStudioTM 7 Flex System using one step PrimeScript® RT-PCR Kit (Takara, RR064 A, Tokyo, Japan). ..

    Article Title: Transcriptome Profiling Reveals That the African Swine Fever Virus C315R Exploits the IL-6 STAT3 Signaling Axis to Facilitate Virus Replication
    Article Snippet: 3D4/21 cells were transfected with 2 μg of either pcDNA3.1-HA (NC control) or pcDNA3.1-HA-C315R for 24 h. Total RNA was extracted from each sample using Trizol (Invitrogen, 15596026, Waltham, MA, USA), and cDNA was synthesized using the PrimeScript RT Reagent Kit with gDNA Eraser (Takara, RR092S, Osaka, Japan) according to the manufacturer’s instructions. .. Reverse transcription PCR (RT-PCR) was performed using the Step PrimeScript RT-PCR Kit (Takara, RR064B, Osaka, Japan). ..

    Article Title: NLRP3 Inflammasome Activation Mediates Hepatitis E Virus-Induced Neuroinflammation.
    Article Snippet: Hepatitis E virus (HEV) is a foodborne zoonotic pathogen that is supposed to be one of the most common causes of acute viral hepatitis.. However, HEV infection has been recently associated with a wide spectrum of extrahepatic manifestations, particularly neurological disorders.. Previous studies have shown that HEV is able to cross the blood–brain barrier (BBB) and induce inflammatory response of the central nervous system.

    Article Title: Transcriptome Profiling Reveals That the African Swine Fever Virus C315R Exploits the IL-6 STAT3 Signaling Axis to Facilitate Virus Replication.
    Article Snippet: 3D4/21 cells were transfected with 2 μg of either pcDNA3.1-HA (NC control) or pcDNA3.1-HA-C315R for 24 h. Total RNA was extracted from each sample using Trizol (Invitrogen, 15596026, Waltham, MA, USA), and cDNA was synthesized using the PrimeScriptTM RT Reagent Kit with gDNA Eraser (Takara, RR092S, Osaka, Japan) according to the manufacturer’s instructions. .. Reverse transcription PCR (RT-PCR) was performed using the Step PrimeScript RT-PCR Kit (Takara, RR064B, Osaka, Japan). ..

    Article Title: Identification of mutations in viral proteins involved in cell adaptation using a reverse genetic system of the live attenuated hepatitis A virus vaccine H2 strain.
    Article Snippet: Reverse transcription-quantitative PCR (RT-qPCR) 148 The virus RNA was extracted from preserved supernatant using a PureLink RNA mini kit 149 (Thermo Fisher Scientific, USA, 12183018A). .. Then, the viral genome was amplified using the 150 One Step PrimeScript RT-PCR kit (Takara, Japan, RR096A). ..

    Article Title: Inhibition of Farnesoid-x-receptor signaling during abdominal sepsis by dysbiosis exacerbates gut barrier dysfunction
    Article Snippet: To determine relative gene expression in the ileum, RNA was isolated by using TRIZOL (Invitrogen, Carlsbard, CA, USA) following the manufacturer’s instructions, and quantified by a NanoDrop1000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA). cDNA was processed with the cDNA synthesis kit (Thermo Fisher Scientific, Waltham, MA, USA) according to the standard protocol. .. RT-qPCR was conducted on the QuantStudioTM 7 Flex System using one step PrimeScript® RT-PCR Kit (Takara, RR064 A, Tokyo, Japan). ..

    Article Title: HSF1–DBC1 axis drives prostate cancer progression by activating a metastatic transcriptional program
    Article Snippet: .. Real-time quantitative reverse transcription-PCR (qRT-PCR) Total RNA was extracted using TRIzol reagent (Invitrogen), and qRT-PCR was performed using the One- step PrimeScript RT-PCR Kit (Takara Bio). qRT-PCR was performed in triplicate using gene-specific primers on QuantStudio 6 Flex real-time PCR system (Applied Biosystems). ..

    Article Title: Characterization of the virus-host RNA-RNA interactome across important human pathogenic RNA viruses.
    Article Snippet: .. SYBR Green RT-qPCR was performed using the One step primescript RT-PCR kit (Takara) according to manufacturer’s instructions. ..

    Reverse Transcription:

    Article Title: Transcriptome Profiling Reveals That the African Swine Fever Virus C315R Exploits the IL-6 STAT3 Signaling Axis to Facilitate Virus Replication
    Article Snippet: 3D4/21 cells were transfected with 2 μg of either pcDNA3.1-HA (NC control) or pcDNA3.1-HA-C315R for 24 h. Total RNA was extracted from each sample using Trizol (Invitrogen, 15596026, Waltham, MA, USA), and cDNA was synthesized using the PrimeScript RT Reagent Kit with gDNA Eraser (Takara, RR092S, Osaka, Japan) according to the manufacturer’s instructions. .. Reverse transcription PCR (RT-PCR) was performed using the Step PrimeScript RT-PCR Kit (Takara, RR064B, Osaka, Japan). ..

    Article Title: NLRP3 Inflammasome Activation Mediates Hepatitis E Virus-Induced Neuroinflammation.
    Article Snippet: Hepatitis E virus (HEV) is a foodborne zoonotic pathogen that is supposed to be one of the most common causes of acute viral hepatitis.. However, HEV infection has been recently associated with a wide spectrum of extrahepatic manifestations, particularly neurological disorders.. Previous studies have shown that HEV is able to cross the blood–brain barrier (BBB) and induce inflammatory response of the central nervous system.

    Article Title: Transcriptome Profiling Reveals That the African Swine Fever Virus C315R Exploits the IL-6 STAT3 Signaling Axis to Facilitate Virus Replication.
    Article Snippet: 3D4/21 cells were transfected with 2 μg of either pcDNA3.1-HA (NC control) or pcDNA3.1-HA-C315R for 24 h. Total RNA was extracted from each sample using Trizol (Invitrogen, 15596026, Waltham, MA, USA), and cDNA was synthesized using the PrimeScriptTM RT Reagent Kit with gDNA Eraser (Takara, RR092S, Osaka, Japan) according to the manufacturer’s instructions. .. Reverse transcription PCR (RT-PCR) was performed using the Step PrimeScript RT-PCR Kit (Takara, RR064B, Osaka, Japan). ..

    Polymerase Chain Reaction:

    Article Title: Transcriptome Profiling Reveals That the African Swine Fever Virus C315R Exploits the IL-6 STAT3 Signaling Axis to Facilitate Virus Replication
    Article Snippet: 3D4/21 cells were transfected with 2 μg of either pcDNA3.1-HA (NC control) or pcDNA3.1-HA-C315R for 24 h. Total RNA was extracted from each sample using Trizol (Invitrogen, 15596026, Waltham, MA, USA), and cDNA was synthesized using the PrimeScript RT Reagent Kit with gDNA Eraser (Takara, RR092S, Osaka, Japan) according to the manufacturer’s instructions. .. Reverse transcription PCR (RT-PCR) was performed using the Step PrimeScript RT-PCR Kit (Takara, RR064B, Osaka, Japan). ..

    Article Title: NLRP3 Inflammasome Activation Mediates Hepatitis E Virus-Induced Neuroinflammation.
    Article Snippet: Hepatitis E virus (HEV) is a foodborne zoonotic pathogen that is supposed to be one of the most common causes of acute viral hepatitis.. However, HEV infection has been recently associated with a wide spectrum of extrahepatic manifestations, particularly neurological disorders.. Previous studies have shown that HEV is able to cross the blood–brain barrier (BBB) and induce inflammatory response of the central nervous system.

    Article Title: Transcriptome Profiling Reveals That the African Swine Fever Virus C315R Exploits the IL-6 STAT3 Signaling Axis to Facilitate Virus Replication.
    Article Snippet: 3D4/21 cells were transfected with 2 μg of either pcDNA3.1-HA (NC control) or pcDNA3.1-HA-C315R for 24 h. Total RNA was extracted from each sample using Trizol (Invitrogen, 15596026, Waltham, MA, USA), and cDNA was synthesized using the PrimeScriptTM RT Reagent Kit with gDNA Eraser (Takara, RR092S, Osaka, Japan) according to the manufacturer’s instructions. .. Reverse transcription PCR (RT-PCR) was performed using the Step PrimeScript RT-PCR Kit (Takara, RR064B, Osaka, Japan). ..

    Amplification:

    Article Title: Identification of mutations in viral proteins involved in cell adaptation using a reverse genetic system of the live attenuated hepatitis A virus vaccine H2 strain.
    Article Snippet: Reverse transcription-quantitative PCR (RT-qPCR) 148 The virus RNA was extracted from preserved supernatant using a PureLink RNA mini kit 149 (Thermo Fisher Scientific, USA, 12183018A). .. Then, the viral genome was amplified using the 150 One Step PrimeScript RT-PCR kit (Takara, Japan, RR096A). ..

    Real-time Polymerase Chain Reaction:

    Article Title: HSF1–DBC1 axis drives prostate cancer progression by activating a metastatic transcriptional program
    Article Snippet: .. Real-time quantitative reverse transcription-PCR (qRT-PCR) Total RNA was extracted using TRIzol reagent (Invitrogen), and qRT-PCR was performed using the One- step PrimeScript RT-PCR Kit (Takara Bio). qRT-PCR was performed in triplicate using gene-specific primers on QuantStudio 6 Flex real-time PCR system (Applied Biosystems). ..

    SYBR Green Assay:

    Article Title: Characterization of the virus-host RNA-RNA interactome across important human pathogenic RNA viruses.
    Article Snippet: .. SYBR Green RT-qPCR was performed using the One step primescript RT-PCR kit (Takara) according to manufacturer’s instructions. ..



    Similar Products

    98
    TaKaRa one step tb green primescript rt pcr kit ii
    One Step Tb Green Primescript Rt Pcr Kit Ii, 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/step+primescript+rt+pcr+kit/PrimeScript+RT-PCR+Kit/pmc13107096-64-9-23
    Average 98 stars, based on 1 article reviews
    one step tb green primescript rt pcr kit ii - by Bioz Stars, 2026-10
    98/100 stars
      Buy from Supplier

    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/step+primescript+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, 2026-10
    98/100 stars
      Buy from Supplier

    96
    TaKaRa one step tb green primescript plus 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 Tb Green Primescript Plus 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/step+primescript+rt+pcr+kit/One-Step+TB+Green+PrimeScript+RT-PCR+Kit+II/pm42138434-535-8-18
    Average 96 stars, based on 1 article reviews
    one step tb green primescript plus rt pcr kit - by Bioz Stars, 2026-10
    96/100 stars
      Buy from Supplier

    98
    TaKaRa step primescript 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.
    Step Primescript 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/step+primescript+rt+pcr+kit/PrimeScript+RT-PCR+Kit/pm42139316-359-8-12
    Average 98 stars, based on 1 article reviews
    step primescript rt pcr kit - by Bioz Stars, 2026-10
    98/100 stars
      Buy from Supplier

    97
    TaKaRa 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.
    One Step 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/step+primescript+rt+pcr+kit/One+Step+PrimeScript+RT-PCR+Kit/pmc13173371-90-10-13
    Average 97 stars, based on 1 article reviews
    one step rt pcr kit - by Bioz Stars, 2026-10
    97/100 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/step+primescript+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, 2026-10
    97/100 stars
      Buy from Supplier

    96
    TaKaRa one step primescript iii rt qpcr mix
    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 Primescript Iii Rt Qpcr Mix, 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/step+primescript+rt+pcr+kit/One+Step+PrimeScript+III+RT-PCR+Kit/pm42087199-347-20-37
    Average 96 stars, based on 1 article reviews
    one step primescript iii rt qpcr mix - by Bioz Stars, 2026-10
    96/100 stars
      Buy from Supplier

    96
    TaKaRa one step tb green primescript rt pcr kit ii rr086a
    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 Tb Green Primescript Rt Pcr Kit Ii Rr086a, 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/step+primescript+rt+pcr+kit/One-Step+TB+Green+PrimeScript+RT-PCR+Kit+II/pm42087199-347-28-37
    Average 96 stars, based on 1 article reviews
    one step tb green primescript rt pcr kit ii rr086a - by Bioz Stars, 2026-10
    96/100 stars
      Buy from Supplier

    98
    TaKaRa one step tb green primescript 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 Tb Green Primescript 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/step+primescript+rt+pcr+kit/PrimeScript+RT-PCR+Kit/pmc13129499-66-31-39
    Average 98 stars, based on 1 article reviews
    one step tb green primescript rt pcr kit - by Bioz Stars, 2026-10
    98/100 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