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smartscribe reverse transcriptase  (TaKaRa)


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    Structured Review

    TaKaRa smartscribe reverse transcriptase
    Smartscribe Reverse Transcriptase, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1126 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/smartscribe+reverse+transcriptase/SMARTScribe+Reverse+Transcriptase/pmc13076092-32-22-25
    Average 96 stars, based on 1126 article reviews
    smartscribe reverse transcriptase - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Immunoprecipitation:

    Article Title: METTL3 mediates m 6 A methylation of ADAM17 to Downregulate ACE2–Ang-(1–7) axis and promote progression of hypertension
    Article Snippet: A minimum of 1 μg total RNA was fragmented with an NEBNext Magnesium RNA fragmentation module (New England Biolabs, Ipswich, MA, USA) by incubating at 94 °C for 5 min. Fragmented RNA, including rRNA, was enriched with m6A antibody–Dynabead complexes through immunoprecipitation. .. Immunoprecipitated RNA was then reverse-transcribed to yield first-strand cDNA via SMARTScribe reverse transcriptase (ClonTech, Japan). ..

    Reverse Transcription:

    Article Title: METTL3 mediates m 6 A methylation of ADAM17 to Downregulate ACE2–Ang-(1–7) axis and promote progression of hypertension
    Article Snippet: A minimum of 1 μg total RNA was fragmented with an NEBNext Magnesium RNA fragmentation module (New England Biolabs, Ipswich, MA, USA) by incubating at 94 °C for 5 min. Fragmented RNA, including rRNA, was enriched with m6A antibody–Dynabead complexes through immunoprecipitation. .. Immunoprecipitated RNA was then reverse-transcribed to yield first-strand cDNA via SMARTScribe reverse transcriptase (ClonTech, Japan). ..

    Article Title: Pan-cancer macrophage atlas uncovers that MHC-II high TAMs induce Treg activation through physical interactions.
    Article Snippet: For bulk RNA-seq, RNA extraction was performed using FastPure Cell/Tissue Total RNA Isolation Kit V2 (Vazyme RC112-01). .. Reverse transcription was performed using SMARTScribe Reverse Transcriptase (Clontech) according to the manufacturer’s instructions. .. The cDNA was amplified and the final library was constructed using TD501 kit (Vazyme).

    Article Title: Mesenchymal stroma cell-derived stem cell factor mediates cross-species compatibility of the hematopoietic stem cell niche
    Article Snippet: RNA was prepared using the miRNeasy Micro Kit (Qiagen). .. Total RNA was eluted in 10ul and 5ul were used for library preparation for next generation sequencing. cDNA was synthesized from 5 μl total RNA using the SmartScribe reverse transcriptase (Takara Bio, SMARTer HV Kit) with a universally tailed poly-dT primer and a template switching oligo followed by amplification for 12 cycles with the Advantage 2 DNA Polymerase (Takara Bio). .. After ultrasonic shearing (Covaris LE220), amplified cDNA samples were subjected to standard Illumina fragment library preparation using the NEBnext Ultra DNA library preparation chemistry (New England Biolabs).

    Article Title: A Recombinant Antibody Against Human DRP1 Serine 616 Phosphorylation Enables Detection of BRAF V600E -Associated Mitochondrial Division in Cancer
    Article Snippet: Sequencing of the 3G11 antibody was performed using SMARTer 5′ RACE technology (Takara Bio, MoutainView, CA, USA, Cat. No. 634858) adapted for immunoglobulins to amplify the variable genes from the heavy and kappa chains from the 3G11 hybridoma. .. Briefly, RNA was extracted from the hybridoma using a RNeasy Mini Kit (Qiagen, Hilden, Germany, Cat. No. 74104), followed by first-strand cDNA synthesis using constant gene-specific 3′ primers (GSP1) based on mouse IgG/mouse kappa constant isotypes and incubation with the SMARTer II A Oligonucleotide and SMARTscribe reverse transcriptase (Takara, MoutainView, CA, USA). ..

    Article Title: Direct-to-library methods, systems, and compositions
    Article Snippet: 2.0 μL 1 μM Poly dT primer (IDT) and 6 μL of SMARTScribe 1st Strand buffer (5×) (Takara, Kusatsu, Japan) was added to the eluate and the resulting mixture incubated at 95° C. for 1 minute before placing on ice. .. The Extension and Template-switching mix was prepared by combining 4.5 μL SMARTScribe 1st Strand buffer (5×) (Takara, Kusatsu, Japan), 0.5 μL dNTP mix (25 mM per nucleotide, Thermo-Fisher Scientific, Waltham, MA), 2.0 μL SMARTScribe Reverse Transcriptase (100 u/μL, Takara, Kusatsu, Japan), 2.0 μL 5 μM Template-switching Oligo (TS Oligo) (IDT), 5.0 μL of DTT (20M, Takara, Kusatsu, Japan), and 4 μL Nuclease-free water. .. The resulting reaction mixture was incubated for 90 min at 42° C. and the reaction was heat denatured at 70° C. for 15 min. Next, 50.0 μL of NEBNext Ultra II Q5 (NEB, Ipswich, MA), and 8.0 μL of indexing primer mixture (NEB, Ipswich, MA) were added to the reaction from the previous step.

    Article Title: Direct-to-library methods, systems, and compositions
    Article Snippet: .. For extension and template switching, 0.5×SMARTScribe RT buffer (Takara, Japan), 2 μM DTT (Takara, Japan), 0.25 mM dNTPs (Thermo-Fisher, Waltham, MA), 200 units of SMARTScribe Reverse Transcriptase (Takara Japan) and template switching oligo (0.2 uM, IDT DNA, Coralville, IA) was added and incubated for 90 minutes at 42° C. followed by 5 cycles of 50° C. for 2 minutes and 42° C. for 2 minutes and 5 cycles of 55° C. for 30 seconds and 42° C. for 2 minutes and then heat denatured at 70° C. for 15 minutes. .. This reaction was then amplified in 1× Terra Direct buffer (Takara, Japan) with 1.25 unit Terra Direct polymerase (Takara, Japan) and 200 nM PCR primers using the following conditions: 98° C. for 2 minutes, 12 cycles of 98° C. for 15 seconds, 60° C. for 30 seconds, 68° C. for 1 minute.

    Article Title: The circadian isoform landscape of mouse livers
    Article Snippet: .. First strand reverse transcription was performed for 1 h at 42°C, before being heat inactivated for 5 min at 70°C, using the Smartscribe Reverse Transcriptase (Clontech). ..

    Article Title: Human antibody targeting Crimean-Congo hemorrhagic fever virus glycoprotein 38 protects mice against heterologous virus challenge
    Article Snippet: .. Post incubation, added to the total RNA reaction was a mixture of 5× first-strand buffer (Clontech), dithiothreitol (20 mM), 5′ template switch oligo (10 μM), deoxynucleotide triphosphate (dNTP) solution (10 mM each), and 10× SMARTScribe Reverse Transcriptase (Clontech) (60 min incubation) at 42°C. .. The first-strand synthesis reaction was purified using Ampure Size Select Magnetic Bead Kit (ratio of 1.8× [Beckman Coulter]).

    Next-Generation Sequencing:

    Article Title: Mesenchymal stroma cell-derived stem cell factor mediates cross-species compatibility of the hematopoietic stem cell niche
    Article Snippet: RNA was prepared using the miRNeasy Micro Kit (Qiagen). .. Total RNA was eluted in 10ul and 5ul were used for library preparation for next generation sequencing. cDNA was synthesized from 5 μl total RNA using the SmartScribe reverse transcriptase (Takara Bio, SMARTer HV Kit) with a universally tailed poly-dT primer and a template switching oligo followed by amplification for 12 cycles with the Advantage 2 DNA Polymerase (Takara Bio). .. After ultrasonic shearing (Covaris LE220), amplified cDNA samples were subjected to standard Illumina fragment library preparation using the NEBnext Ultra DNA library preparation chemistry (New England Biolabs).

    Synthesized:

    Article Title: Mesenchymal stroma cell-derived stem cell factor mediates cross-species compatibility of the hematopoietic stem cell niche
    Article Snippet: RNA was prepared using the miRNeasy Micro Kit (Qiagen). .. Total RNA was eluted in 10ul and 5ul were used for library preparation for next generation sequencing. cDNA was synthesized from 5 μl total RNA using the SmartScribe reverse transcriptase (Takara Bio, SMARTer HV Kit) with a universally tailed poly-dT primer and a template switching oligo followed by amplification for 12 cycles with the Advantage 2 DNA Polymerase (Takara Bio). .. After ultrasonic shearing (Covaris LE220), amplified cDNA samples were subjected to standard Illumina fragment library preparation using the NEBnext Ultra DNA library preparation chemistry (New England Biolabs).

    Amplification:

    Article Title: Mesenchymal stroma cell-derived stem cell factor mediates cross-species compatibility of the hematopoietic stem cell niche
    Article Snippet: RNA was prepared using the miRNeasy Micro Kit (Qiagen). .. Total RNA was eluted in 10ul and 5ul were used for library preparation for next generation sequencing. cDNA was synthesized from 5 μl total RNA using the SmartScribe reverse transcriptase (Takara Bio, SMARTer HV Kit) with a universally tailed poly-dT primer and a template switching oligo followed by amplification for 12 cycles with the Advantage 2 DNA Polymerase (Takara Bio). .. After ultrasonic shearing (Covaris LE220), amplified cDNA samples were subjected to standard Illumina fragment library preparation using the NEBnext Ultra DNA library preparation chemistry (New England Biolabs).

    cDNA Synthesis:

    Article Title: A Recombinant Antibody Against Human DRP1 Serine 616 Phosphorylation Enables Detection of BRAF V600E -Associated Mitochondrial Division in Cancer
    Article Snippet: Sequencing of the 3G11 antibody was performed using SMARTer 5′ RACE technology (Takara Bio, MoutainView, CA, USA, Cat. No. 634858) adapted for immunoglobulins to amplify the variable genes from the heavy and kappa chains from the 3G11 hybridoma. .. Briefly, RNA was extracted from the hybridoma using a RNeasy Mini Kit (Qiagen, Hilden, Germany, Cat. No. 74104), followed by first-strand cDNA synthesis using constant gene-specific 3′ primers (GSP1) based on mouse IgG/mouse kappa constant isotypes and incubation with the SMARTer II A Oligonucleotide and SMARTscribe reverse transcriptase (Takara, MoutainView, CA, USA). ..

    Incubation:

    Article Title: A Recombinant Antibody Against Human DRP1 Serine 616 Phosphorylation Enables Detection of BRAF V600E -Associated Mitochondrial Division in Cancer
    Article Snippet: Sequencing of the 3G11 antibody was performed using SMARTer 5′ RACE technology (Takara Bio, MoutainView, CA, USA, Cat. No. 634858) adapted for immunoglobulins to amplify the variable genes from the heavy and kappa chains from the 3G11 hybridoma. .. Briefly, RNA was extracted from the hybridoma using a RNeasy Mini Kit (Qiagen, Hilden, Germany, Cat. No. 74104), followed by first-strand cDNA synthesis using constant gene-specific 3′ primers (GSP1) based on mouse IgG/mouse kappa constant isotypes and incubation with the SMARTer II A Oligonucleotide and SMARTscribe reverse transcriptase (Takara, MoutainView, CA, USA). ..

    Article Title: Direct-to-library methods, systems, and compositions
    Article Snippet: .. For extension and template switching, 0.5×SMARTScribe RT buffer (Takara, Japan), 2 μM DTT (Takara, Japan), 0.25 mM dNTPs (Thermo-Fisher, Waltham, MA), 200 units of SMARTScribe Reverse Transcriptase (Takara Japan) and template switching oligo (0.2 uM, IDT DNA, Coralville, IA) was added and incubated for 90 minutes at 42° C. followed by 5 cycles of 50° C. for 2 minutes and 42° C. for 2 minutes and 5 cycles of 55° C. for 30 seconds and 42° C. for 2 minutes and then heat denatured at 70° C. for 15 minutes. .. This reaction was then amplified in 1× Terra Direct buffer (Takara, Japan) with 1.25 unit Terra Direct polymerase (Takara, Japan) and 200 nM PCR primers using the following conditions: 98° C. for 2 minutes, 12 cycles of 98° C. for 15 seconds, 60° C. for 30 seconds, 68° C. for 1 minute.

    Article Title: Human antibody targeting Crimean-Congo hemorrhagic fever virus glycoprotein 38 protects mice against heterologous virus challenge
    Article Snippet: .. Post incubation, added to the total RNA reaction was a mixture of 5× first-strand buffer (Clontech), dithiothreitol (20 mM), 5′ template switch oligo (10 μM), deoxynucleotide triphosphate (dNTP) solution (10 mM each), and 10× SMARTScribe Reverse Transcriptase (Clontech) (60 min incubation) at 42°C. .. The first-strand synthesis reaction was purified using Ampure Size Select Magnetic Bead Kit (ratio of 1.8× [Beckman Coulter]).



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