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ex premier dna polymerase dye plus  (TaKaRa)


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    Structured Review

    TaKaRa ex premier dna polymerase dye plus
    Ex Premier Dna Polymerase Dye Plus, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 229 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ex+premier+dna+polymerase+dye+plus/Takara+Ex+Premier/pm42080289-123-1-0
    Average 96 stars, based on 229 article reviews
    ex premier dna polymerase dye plus - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    other:

    Article Title: Metatranscriptomic identification of novel RNA viruses from raccoon dog ( Nyctereutes procyonoides ) feces in Japan
    Article Snippet: For both frequency investigation and complete genome determination, PrimeScriptTM RT Master Mix (Takara Bio) and TaKaRa Ex PremierTM DNA Polymerase Dye plus (Takara Bio) were used for RT and PCR, respectively.

    Article Title: Evolution and diversification of the momilactone biosynthetic gene cluster in the genus Oryza
    Article Snippet: The PCR was carried out using Ex PremierTM DNA Polymerase Dye Plus (TaKaRa).

    Cloning:

    Article Title: Engineering a self-organized enzyme cascade for enhanced cell-free biosynthesis of 3-hydroxypropionic acid.
    Article Snippet: .. TaKaRa Ex Premier DNA Polymerase Dye Plus (2 ) from TaKaRa (Kusatsu, Japan) was used for cloning procedures. .. Plasmid DNA was isolated using plasmid extraction kits (Bioneer, Daejeon, Korea).

    Amplification:

    Article Title: Emergence of a natural reassortant between Shamonda and Sathuperi viruses of the species Orthobunyavirus schmallenbergense in Japan.
    Article Snippet: contains epitopes targeted by neutralizing antibodies, and the selection pressure by the hosts' immune systems results in a high degree of diversity of the Gc coding sequence in the M RNA segment among particular orthobunyaviruses [3].. Whole-genome sequencing and phylogenetic analysis of a large number of orthobunyaviruses has revealed that multiple instances of reassortment have occurred during the evolution of orthobunyaviruses [3].. Such reassortments might have generated novel human and animal pathogens, as has been suggested in the case of Ngari virus, which is associated with human hemorrhagic disease [4].

    Virus:

    Article Title: Emergence of a natural reassortant between Shamonda and Sathuperi viruses of the species Orthobunyavirus schmallenbergense in Japan.
    Article Snippet: contains epitopes targeted by neutralizing antibodies, and the selection pressure by the hosts' immune systems results in a high degree of diversity of the Gc coding sequence in the M RNA segment among particular orthobunyaviruses [3].. Whole-genome sequencing and phylogenetic analysis of a large number of orthobunyaviruses has revealed that multiple instances of reassortment have occurred during the evolution of orthobunyaviruses [3].. Such reassortments might have generated novel human and animal pathogens, as has been suggested in the case of Ngari virus, which is associated with human hemorrhagic disease [4].

    Polymerase Chain Reaction:

    Article Title: Isolation and identification of avian leukosis virus subgroup J from Luohé Ma chicken.
    Article Snippet: Henan Province is rich in livestock and poultry resources, home to well-known local breeds, including Gushi, Lushi, and Luohé Ma chickens.. These breeds are of substantial agricultural and economic importance and play a pivotal role in preserving biodiversity as well as fostering genetic innovation.. Avian leukosis (AL) is a major viral disease affecting the poultry industry, with the J subgroup of avian leukosis virus (ALV-J) emerging as a significant cause of economic losses.

    Article Title: Long-read sequencing of the ATP7B gene from Moroccan patients with suspected Wilson disease
    Article Snippet: .. The PCR mixture consisted of 12.5 μL of Takara Ex-Premier DNA Polymerase Dye plus (cat. #RR371A), 10.5 μL of nuclease-free H2O, and 1 μL of 10 pmol/μL forward and reverse primers ( ). ..

    Article Title: Identification of multiple inter- and intra-genotype reassortment mammalian orthoreoviruses from Japanese black cattle in a beef cattle farm
    Article Snippet: For MRV genotyping RT-PCR, RNA was extracted from the supernatant of cell culture using TRIzol LS Reagent (Life Technologies) and reverse transcription was performed using the PrimeScriptTM Reverse Transcriptase (Takara Bio) with random primers. .. PCR with MRV genotype discrimination primers designed in this study (Supplementary Table ) was performed using TaKaRa Ex Premier DNA Polymerase Dye plus (TaKaRa bio). ..



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