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primescripttm rt qpcr kit  (TaKaRa)


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    Structured Review

    TaKaRa primescripttm rt qpcr kit
    Primescripttm Rt Qpcr Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 88818 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primescripttm+rt+reagent+kit+for+qpcr/PrimeScript+RT+Reagent+Kit/pm42092926-370-11-14
    Average 99 stars, based on 88818 article reviews
    primescripttm rt qpcr kit - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Software:

    Article Title: Iron Deficiency Leads to Chlorosis Through Impacting Chlorophyll Synthesis and Nitrogen Metabolism in Areca catechu L.
    Article Snippet: .. All DEGs were analyzed by GO enrichment using GOseq (1.10.0) (Young et al., 2010) and KEGG enrichment using KOBAS software (Mao et al., 2005; Minoru et al., 2016). qPCR Analysis The extracted RNA of normal and albinotic leaf samples were converted into cDNA using PrimeScriptTM RT reagent Kit for qPCR (RR047Q, TaKaRa, Japan). ..

    Real-time Polymerase Chain Reaction:

    Article Title: Iron Deficiency Leads to Chlorosis Through Impacting Chlorophyll Synthesis and Nitrogen Metabolism in Areca catechu L.
    Article Snippet: .. All DEGs were analyzed by GO enrichment using GOseq (1.10.0) (Young et al., 2010) and KEGG enrichment using KOBAS software (Mao et al., 2005; Minoru et al., 2016). qPCR Analysis The extracted RNA of normal and albinotic leaf samples were converted into cDNA using PrimeScriptTM RT reagent Kit for qPCR (RR047Q, TaKaRa, Japan). ..

    Article Title: Identification of genes regulated by the two-component system response regulator NarP of Actinobacillus pleuropneumoniae via DNA-affinity-purified sequencing.
    Article Snippet: RNA was extracted from 3ml of the cells using the SV Total RNA Isolation System (Promega, Madison, USA). .. RNA was treated with gDNA Eraser (Takara, Beijing, China) to remove the contaminated chromosome DNA, which was subsequently used as template for reverse transcription using the PrimeScriptTM RT reagent Kit for qPCR (Takara, Beijing, China). qPCR was carried out using the cDNA as template and the SYBR® Premix Ex TaqTM II kit (TOYOBO, Osaka, Japan) with the primers listed in Table S1. ..

    Article Title: Phytohormones and candidate genes synergistically regulate fruitlet abscission in Areca catechu L.
    Article Snippet: Samples were sputter coated with gold, and were viewed at 5 kV on a Hitachi SU8100 Field Emission Scanning Electron Microscope. .. For the morphology analysis, the samples were collected from different individuals at least three times. qPCR analysis The extracted RNA of AB and CK samples were reversely transcripted into cDNA using the PrimeScriptTM RT reagent Kit for qPCR (TaKaRa, Japan). .. The qPCR reaction was performed using the PowerUpTM SYBRTM Green Master Mix (Applied Biosystems, United States) in an Applied Biosystem 7500 real-time PCR system.

    Article Title: Treat the “Untreatable” by a Photothermal Agent: Triggering Heat and Immunological Responses for Rabies Virus Inactivation
    Article Snippet: .. RNA isolation and quantitative real-time PCR (qPCR) The mouse brains and muscles were homogenized separately and centrifuged at 4 °C, 8000 r.p.m. for 5 min. RNA was isolated from the cell pellet using TRIzol reagent (0.1 g/ml) according to the manufacturer’s instructions (TIANGEN, China) and reverse transcribed into cDNA using the PrimeScriptTM RT reagent Kit for qPCR (TAKARA, Japan). ..

    Reverse Transcription:

    Article Title: Identification of genes regulated by the two-component system response regulator NarP of Actinobacillus pleuropneumoniae via DNA-affinity-purified sequencing.
    Article Snippet: RNA was extracted from 3ml of the cells using the SV Total RNA Isolation System (Promega, Madison, USA). .. RNA was treated with gDNA Eraser (Takara, Beijing, China) to remove the contaminated chromosome DNA, which was subsequently used as template for reverse transcription using the PrimeScriptTM RT reagent Kit for qPCR (Takara, Beijing, China). qPCR was carried out using the cDNA as template and the SYBR® Premix Ex TaqTM II kit (TOYOBO, Osaka, Japan) with the primers listed in Table S1. ..

    Article Title: Treat the “Untreatable” by a Photothermal Agent: Triggering Heat and Immunological Responses for Rabies Virus Inactivation
    Article Snippet: .. RNA isolation and quantitative real-time PCR (qPCR) The mouse brains and muscles were homogenized separately and centrifuged at 4 °C, 8000 r.p.m. for 5 min. RNA was isolated from the cell pellet using TRIzol reagent (0.1 g/ml) according to the manufacturer’s instructions (TIANGEN, China) and reverse transcribed into cDNA using the PrimeScriptTM RT reagent Kit for qPCR (TAKARA, Japan). ..

    Isolation:

    Article Title: Treat the “Untreatable” by a Photothermal Agent: Triggering Heat and Immunological Responses for Rabies Virus Inactivation
    Article Snippet: .. RNA isolation and quantitative real-time PCR (qPCR) The mouse brains and muscles were homogenized separately and centrifuged at 4 °C, 8000 r.p.m. for 5 min. RNA was isolated from the cell pellet using TRIzol reagent (0.1 g/ml) according to the manufacturer’s instructions (TIANGEN, China) and reverse transcribed into cDNA using the PrimeScriptTM RT reagent Kit for qPCR (TAKARA, Japan). ..

    Muscles:

    Article Title: Treat the “Untreatable” by a Photothermal Agent: Triggering Heat and Immunological Responses for Rabies Virus Inactivation
    Article Snippet: .. RNA isolation and quantitative real-time PCR (qPCR) The mouse brains and muscles were homogenized separately and centrifuged at 4 °C, 8000 r.p.m. for 5 min. RNA was isolated from the cell pellet using TRIzol reagent (0.1 g/ml) according to the manufacturer’s instructions (TIANGEN, China) and reverse transcribed into cDNA using the PrimeScriptTM RT reagent Kit for qPCR (TAKARA, Japan). ..



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