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superscript ii cdna synthesis kit  (Sangon Biotech)

 
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    Sangon Biotech superscript ii cdna synthesis kit
    Superscript Ii Cdna Synthesis Kit, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/superscript+cdna+kit/cdna+first+kit+mirna+strand+synthesis/pm42277600-52-21-26
    Average 86 stars, based on 1 article reviews
    superscript ii cdna synthesis kit - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    other:

    Article Title: Aqueous extracts from asparagus stems prevent memory impairments in scopolamine-treated mice.
    Article Snippet: Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content.. The journal’s standard Terms & Conditions and the ethical guidelines, outlined in our author and reviewer resource centre, still apply.. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains.

    cDNA Synthesis:

    Article Title: FTO-Catalysed Demethylation of LUR1 mRNA Suppresses Macrophage Lipid Accumulation and Aortic Atherosclerosis.
    Article Snippet: .. RNA was extracted using TRIzol Reagent (Sangon Biotech, B511311, China). cDNA was prepared by amplifying 500 ng of RNA with a SuperScript- II cDNA Synthesis Kit (Sangon Biotech, B639277, China). .. Quantitative PCR was performed using a RevertAid First Strand cDNA Synthesis Kit (Sangon Biotech, B300538, China) with 1 mg of RNA, and qRT–PCR was performed using an UltraSYBR One Step RT–qPCR Kit (Sangon Biotech, B300540, China) following the manufacturer's instructions.



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    RT-PCR analysis revealed the endogenous expression of krt4, krtt1c19e, notch1a, notch 2, notch 3, and dlc in keratinocytes. These cells were FACS-sorted for EGFP+ cells from Tg(krt4:lyn-EGFP ) and for tdTomato+ cells from Tg(krtt1c19e:tdTomato ). Whole genome cDNA was used as a positive control, and reactions without a template served as negative controls. Figure 4—figure supplement 1—source data 1. Original gel images for RT-PCR analysis displayed in , with labels. Figure 4—figure supplement 1—source data 2. Original files for RT-PCR analysis displayed in , without labels.

    Journal: eLife

    Article Title: Cytoneme-mediated intercellular signaling in keratinocytes is essential for epidermal remodeling in zebrafish

    doi: 10.7554/eLife.97400

    Figure Lengend Snippet: RT-PCR analysis revealed the endogenous expression of krt4, krtt1c19e, notch1a, notch 2, notch 3, and dlc in keratinocytes. These cells were FACS-sorted for EGFP+ cells from Tg(krt4:lyn-EGFP ) and for tdTomato+ cells from Tg(krtt1c19e:tdTomato ). Whole genome cDNA was used as a positive control, and reactions without a template served as negative controls. Figure 4—figure supplement 1—source data 1. Original gel images for RT-PCR analysis displayed in , with labels. Figure 4—figure supplement 1—source data 2. Original files for RT-PCR analysis displayed in , without labels.

    Article Snippet: Commercial assay or kit , SuperScript III CellsDirect cDNA Synthesis Kit , Fisher Scientific , 18-080-200 , .

    Techniques: Reverse Transcription Polymerase Chain Reaction, Expressing, Positive Control