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candidate genes genomic dna  (Thermo Fisher)


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    Structured Review

    Thermo Fisher candidate genes genomic dna
    Candidate Genes Genomic Dna, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 465742 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/candidate genes genomic dna/product/Thermo Fisher
    Average 99 stars, based on 465742 article reviews
    candidate genes genomic dna - by Bioz Stars, 2026-02
    99/100 stars

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    Santa Cruz Biotechnology genomic dna reference sequences of candidate gene prrt2
    (A) Sequencing chromatograms indicating the <t>PRRT2</t> variants detected in family A. (a) The mutated sequence and (b) the wild-type sequence. (B) Sequencing chromatograms displaying the PRRT2 variants detected in family B. (a) The mutated sequence and (b) the wild-type sequence. (C) Sequencing chromatograms indicating the PRRT2 variants detected in family C. (a) The mutated sequence and (b) the wild-type sequence. The red arrows indicate the variant site. Position numbers are displayed above the sequences. PRRT2, proline-rich transmembrane protein 2.
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    Thermo Fisher candidate genes genomic dna amplification
    (A) Sequencing chromatograms indicating the <t>PRRT2</t> variants detected in family A. (a) The mutated sequence and (b) the wild-type sequence. (B) Sequencing chromatograms displaying the PRRT2 variants detected in family B. (a) The mutated sequence and (b) the wild-type sequence. (C) Sequencing chromatograms indicating the PRRT2 variants detected in family C. (a) The mutated sequence and (b) the wild-type sequence. The red arrows indicate the variant site. Position numbers are displayed above the sequences. PRRT2, proline-rich transmembrane protein 2.
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    Image Search Results


    (A) Sequencing chromatograms indicating the PRRT2 variants detected in family A. (a) The mutated sequence and (b) the wild-type sequence. (B) Sequencing chromatograms displaying the PRRT2 variants detected in family B. (a) The mutated sequence and (b) the wild-type sequence. (C) Sequencing chromatograms indicating the PRRT2 variants detected in family C. (a) The mutated sequence and (b) the wild-type sequence. The red arrows indicate the variant site. Position numbers are displayed above the sequences. PRRT2, proline-rich transmembrane protein 2.

    Journal: Experimental and Therapeutic Medicine

    Article Title: Novel PRRT2 gene variants identified in paroxysmal kinesigenic dyskinesia and benign familial infantile epilepsy in Chinese families

    doi: 10.3892/etm.2021.9935

    Figure Lengend Snippet: (A) Sequencing chromatograms indicating the PRRT2 variants detected in family A. (a) The mutated sequence and (b) the wild-type sequence. (B) Sequencing chromatograms displaying the PRRT2 variants detected in family B. (a) The mutated sequence and (b) the wild-type sequence. (C) Sequencing chromatograms indicating the PRRT2 variants detected in family C. (a) The mutated sequence and (b) the wild-type sequence. The red arrows indicate the variant site. Position numbers are displayed above the sequences. PRRT2, proline-rich transmembrane protein 2.

    Article Snippet: Genomic DNA reference sequences of candidate gene PRRT2 (NM_001256442.2) were obtained from the University of California Santa Cruz (UCSC) Genome Browser database ( http://genome.ucsc.edu/ ).

    Techniques: Sequencing, Variant Assay