Review



465767_mat  (Thermo Fisher)


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  • 94

    Structured Review

    Thermo Fisher 465767_mat
    465767 Mat, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/465767_mat/465767_mat/pmc06370886-336-66-34
    Average 94 stars, based on 1 article reviews
    465767_mat - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Injection:

    Article Title: A cell cycle-coordinated Polymerase II transcription compartment encompasses gene expression before global genome activation
    Article Snippet: Three RNA samples for each group (MOs injected and non-injected) from three independent experiments were prepared. cDNA was synthesized from equal amounts of total RNA (100 ng) using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer’s protocol. cDNA samples were diluted 1:30 with nuclease-free water. qPCR reactions were prepared using the ddSupermix for Probes (Bio-rad) and Taqman miRNA probes miR430a (004365_mat) and miR430b (465767_mat).

    Article Title: A cell cycle-coordinated nuclear compartment for Polymerase II transcription encompasses the earliest gene expression before global genome activation
    Article Snippet: Three RNA samples for each group (MOs injected and noninjected) from three independent experiments were prepared. cDNA was synthesized from equal amounts of total RNA (100ng) using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer’s protocol. cDNA samples were diluted 1:30 with nuclease-free water. qPCR reactions were prepared using the ddSupermix for Probes (Bio-rad) and Taqman miRNA probes miR430a (004365_mat) and miR430b (465767_mat).

    Synthesized:

    Article Title: A cell cycle-coordinated Polymerase II transcription compartment encompasses gene expression before global genome activation
    Article Snippet: Three RNA samples for each group (MOs injected and non-injected) from three independent experiments were prepared. cDNA was synthesized from equal amounts of total RNA (100 ng) using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer’s protocol. cDNA samples were diluted 1:30 with nuclease-free water. qPCR reactions were prepared using the ddSupermix for Probes (Bio-rad) and Taqman miRNA probes miR430a (004365_mat) and miR430b (465767_mat).

    Article Title: A cell cycle-coordinated nuclear compartment for Polymerase II transcription encompasses the earliest gene expression before global genome activation
    Article Snippet: Three RNA samples for each group (MOs injected and noninjected) from three independent experiments were prepared. cDNA was synthesized from equal amounts of total RNA (100ng) using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer’s protocol. cDNA samples were diluted 1:30 with nuclease-free water. qPCR reactions were prepared using the ddSupermix for Probes (Bio-rad) and Taqman miRNA probes miR430a (004365_mat) and miR430b (465767_mat).

    Reverse Transcription:

    Article Title: A cell cycle-coordinated Polymerase II transcription compartment encompasses gene expression before global genome activation
    Article Snippet: Three RNA samples for each group (MOs injected and non-injected) from three independent experiments were prepared. cDNA was synthesized from equal amounts of total RNA (100 ng) using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer’s protocol. cDNA samples were diluted 1:30 with nuclease-free water. qPCR reactions were prepared using the ddSupermix for Probes (Bio-rad) and Taqman miRNA probes miR430a (004365_mat) and miR430b (465767_mat).

    Article Title: A cell cycle-coordinated nuclear compartment for Polymerase II transcription encompasses the earliest gene expression before global genome activation
    Article Snippet: Three RNA samples for each group (MOs injected and noninjected) from three independent experiments were prepared. cDNA was synthesized from equal amounts of total RNA (100ng) using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer’s protocol. cDNA samples were diluted 1:30 with nuclease-free water. qPCR reactions were prepared using the ddSupermix for Probes (Bio-rad) and Taqman miRNA probes miR430a (004365_mat) and miR430b (465767_mat).

    Real-time Polymerase Chain Reaction:

    Article Title: A cell cycle-coordinated Polymerase II transcription compartment encompasses gene expression before global genome activation
    Article Snippet: Three RNA samples for each group (MOs injected and non-injected) from three independent experiments were prepared. cDNA was synthesized from equal amounts of total RNA (100 ng) using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer’s protocol. cDNA samples were diluted 1:30 with nuclease-free water. qPCR reactions were prepared using the ddSupermix for Probes (Bio-rad) and Taqman miRNA probes miR430a (004365_mat) and miR430b (465767_mat).

    Article Title: A cell cycle-coordinated nuclear compartment for Polymerase II transcription encompasses the earliest gene expression before global genome activation
    Article Snippet: Three RNA samples for each group (MOs injected and noninjected) from three independent experiments were prepared. cDNA was synthesized from equal amounts of total RNA (100ng) using the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems) following the manufacturer’s protocol. cDNA samples were diluted 1:30 with nuclease-free water. qPCR reactions were prepared using the ddSupermix for Probes (Bio-rad) and Taqman miRNA probes miR430a (004365_mat) and miR430b (465767_mat).



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