uv transilluminator geldoc-it imaging system (EuroClone)
90
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EuroClone
uv transilluminator geldoc-it imaging system
Uv Transilluminator Geldoc It Imaging System, supplied by EuroClone, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/uv+transilluminator+geldoc-it+imaging+system/uv+transilluminator+geldoc+it+imaging+system/pmc09866474-88-6-11
Average 90 stars, based on 1 article reviews
Uv Transilluminator Geldoc It Imaging System, supplied by EuroClone, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/uv+transilluminator+geldoc-it+imaging+system/uv+transilluminator+geldoc+it+imaging+system/pmc09866474-88-6-11
Average 90 stars, based on 1 article reviews
uv transilluminator geldoc-it imaging system - by Bioz Stars,
2026-11
90/100 stars
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Imaging:Article Title: Occurrence and Molecular Characterization of Potentially Pathogenic Vibrio spp. in Seafood Collected in Sicily Article Snippet: PCR assays targeting ToxR and VVH loci were performed under the following conditions: a first step denaturation at 96 °C for 5 min and 30 cycles of a 3-step amplification (denaturation at 94 °C for 1 min, annealing at 63 °C for 1.5 min, and extension at 72 °C for 1.5 min), followed by a final extension step at 72 °C for 7 min. PCR assays targeting the VC locus were performed under the following conditions: a first step denaturation at 94 °C for 2 min and 30 cycles of a 3-step amplification (denaturation at 94 °C for 1 min, annealing at 50 °C for 1 min, and extension at 72 °C for 1.5 min) followed by a final extension step at 72 °C for 10 min. PCR assays targeting tdh and trh loci were performed under the following conditions: a first step denaturation at 94 °C for 3 min and 30 cycles of a 3-step amplification (denaturation at 94 °C for 1 min, annealing at 58 °C for 1 min, and extension at 72 °C for 1 min) followed by a final extension step at 72 °C for 5 min. After PCR amplification, 10 μL of each reaction product were loaded into 2.0% agarose gels in Tris-acetate-EDTA buffer (Bio-Rad Laboratories, Hercules, CA, USA), containing 5 μL SYBR ® Safe DNA gel stain (Thermo Fisher Scientific, Waltham, MA, USA). .. The amplicons were visualized under a |