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rapid bacterial genomic dna isolation kit  (Sangon Biotech)

 
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    Sangon Biotech rapid bacterial genomic dna isolation kit
    Rapid Bacterial Genomic Dna Isolation 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/bacterial+genome+dna/column+dna+extraction+gel+kit+sanprep/pmc13267575-116-9-16
    Average 86 stars, based on 1 article reviews
    rapid bacterial genomic dna isolation kit - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    Purification:

    Article Title: Enhanced nitrogen removal via simultaneous nitrification and denitrification by a newly isolated strain Enterobacter cloacae GW6 from estuarine sediment
    Article Snippet: .. The genome DNA of Strain GW6 was extracted and purified by using the bacterial genome DNA-extracting kit (Sangon Biotech, Shanghai, China). ..

    Article Title: Enhanced nitrogen removal via simultaneous nitrification and denitrification by a newly isolated strain Enterobacter cloacae GW6 from estuarine sediment
    Article Snippet: .. To identify Strain GW6, the genomic DNA of the strain was extracted and purified by using a bacterial genome DNA-extracting kit (Sangon Biotech, Shanghai, China), and the 16S rRNA gene was amplified by PCR. ..

    Amplification:

    Article Title: Enhanced nitrogen removal via simultaneous nitrification and denitrification by a newly isolated strain Enterobacter cloacae GW6 from estuarine sediment
    Article Snippet: .. To identify Strain GW6, the genomic DNA of the strain was extracted and purified by using a bacterial genome DNA-extracting kit (Sangon Biotech, Shanghai, China), and the 16S rRNA gene was amplified by PCR. ..

    Polymerase Chain Reaction:

    Article Title: Enhanced nitrogen removal via simultaneous nitrification and denitrification by a newly isolated strain Enterobacter cloacae GW6 from estuarine sediment
    Article Snippet: .. To identify Strain GW6, the genomic DNA of the strain was extracted and purified by using a bacterial genome DNA-extracting kit (Sangon Biotech, Shanghai, China), and the 16S rRNA gene was amplified by PCR. ..



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    Antibacterial mechanisms of ZnO@PEG200 QDs against Uropathogenic E. coli CFT073. (A) Zeta potential analysis of electrostatic interaction between ZnO@PEG200 QDs <t>and</t> <t>bacterial</t> surfaces. (B) Zn 2+ concentrations released by ZnO@PEG200 QDs at pH = 7.4 (C) Membrane fluidity disruption assessed by ANS fluorescence. (D) Agarose gel electrophoresis of CFT073 <t>DNA</t> after ZnO@PEG200 QD treatment. (E) DCFH-DA assay for intracellular ROS generation. (F) Dose-dependent O₂ − production measured by absorbance. (G) Relative mRNA expression of virulence genes (FimH, FliC, papG, gapA, FimA, motA) in CFT073, normalized to nusA, showing downregulation of adhesion/motility genes.
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    Image Search Results


    Antibacterial mechanisms of ZnO@PEG200 QDs against Uropathogenic E. coli CFT073. (A) Zeta potential analysis of electrostatic interaction between ZnO@PEG200 QDs and bacterial surfaces. (B) Zn 2+ concentrations released by ZnO@PEG200 QDs at pH = 7.4 (C) Membrane fluidity disruption assessed by ANS fluorescence. (D) Agarose gel electrophoresis of CFT073 DNA after ZnO@PEG200 QD treatment. (E) DCFH-DA assay for intracellular ROS generation. (F) Dose-dependent O₂ − production measured by absorbance. (G) Relative mRNA expression of virulence genes (FimH, FliC, papG, gapA, FimA, motA) in CFT073, normalized to nusA, showing downregulation of adhesion/motility genes.

    Journal: International Journal of Pharmaceutics: X

    Article Title: Precision PEGylation of ZnO quantum dots enables selective intracellular killing of Uropathogenic E. coli via multimodal antibacterial mechanisms without inducing resistance

    doi: 10.1016/j.ijpx.2025.100479

    Figure Lengend Snippet: Antibacterial mechanisms of ZnO@PEG200 QDs against Uropathogenic E. coli CFT073. (A) Zeta potential analysis of electrostatic interaction between ZnO@PEG200 QDs and bacterial surfaces. (B) Zn 2+ concentrations released by ZnO@PEG200 QDs at pH = 7.4 (C) Membrane fluidity disruption assessed by ANS fluorescence. (D) Agarose gel electrophoresis of CFT073 DNA after ZnO@PEG200 QD treatment. (E) DCFH-DA assay for intracellular ROS generation. (F) Dose-dependent O₂ − production measured by absorbance. (G) Relative mRNA expression of virulence genes (FimH, FliC, papG, gapA, FimA, motA) in CFT073, normalized to nusA, showing downregulation of adhesion/motility genes.

    Article Snippet: The Bacterial DNA Genome Kit was obtained from Sangon Biotech (China).

    Techniques: Zeta Potential Analyzer, Membrane, Disruption, Fluorescence, Agarose Gel Electrophoresis, DCFH-DA Assay, Expressing