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electrode gap electroporation cuvette  (Bio-Rad)


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    Structured Review

    Bio-Rad electrode gap electroporation cuvette
    Electrode Gap Electroporation Cuvette, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 848 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/electrode+gap+electroporation+cuvette/pm41053365-182-16-20?v=Bio-Rad
    Average 96 stars, based on 848 article reviews
    electrode gap electroporation cuvette - by Bioz Stars, 2026-07
    96/100 stars

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    Image Search Results


    The composition of used  electroporation  buffers.

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Effects of buffer composition and plasmid toxicity on electroporation-based non-viral gene delivery in mammalian cells using bursts of nanosecond and microsecond pulses

    doi: 10.3389/fbioe.2024.1430637

    Figure Lengend Snippet: The composition of used electroporation buffers.

    Article Snippet: Electroctroporation experiments were performed using a 3 kV, 100 ns–1 m square-wave pulse generator (VilniusTECH, Vilnius, Lithuania) ( ) and a commercially available electroporation cuvette with a 1 mm gap between electrodes (Biorad, Hercules, United States).

    Techniques: Electroporation

    CHO-K1 cell line electrotransfection efficiency dependence on EP buffers composition (No. 1–8) and applied protocols with pEGFP-N1 plasmid encoding green fluorescent protein (GFP). Dashed line indicates average transfection efficacy using 1.2 kV/cm × 100 μs × 8 protocol and electroporation buffer No.1, which serves as a positive control. Asterisk (*) corresponds to statistically significant differences ( p < 0.05) versus positive control.

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Effects of buffer composition and plasmid toxicity on electroporation-based non-viral gene delivery in mammalian cells using bursts of nanosecond and microsecond pulses

    doi: 10.3389/fbioe.2024.1430637

    Figure Lengend Snippet: CHO-K1 cell line electrotransfection efficiency dependence on EP buffers composition (No. 1–8) and applied protocols with pEGFP-N1 plasmid encoding green fluorescent protein (GFP). Dashed line indicates average transfection efficacy using 1.2 kV/cm × 100 μs × 8 protocol and electroporation buffer No.1, which serves as a positive control. Asterisk (*) corresponds to statistically significant differences ( p < 0.05) versus positive control.

    Article Snippet: Electroctroporation experiments were performed using a 3 kV, 100 ns–1 m square-wave pulse generator (VilniusTECH, Vilnius, Lithuania) ( ) and a commercially available electroporation cuvette with a 1 mm gap between electrodes (Biorad, Hercules, United States).

    Techniques: Plasmid Preparation, Transfection, Electroporation, Positive Control

    CHO-K1 cells viability dependence on EP buffers composition (No. 1, 2, 5, and 7) and applied protocols with pEGFP-N1 plasmid encoding green fluorescent protein (GFP). Dot line indicates transfection efficacy using 1.2 kV/cm × 100 μs × 8 protocol. CTRL refers to cells with plasmid in different buffer without electroporation treatment. Asterisk (*) corresponds to statistically significant differences ( p < 0.05).

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Effects of buffer composition and plasmid toxicity on electroporation-based non-viral gene delivery in mammalian cells using bursts of nanosecond and microsecond pulses

    doi: 10.3389/fbioe.2024.1430637

    Figure Lengend Snippet: CHO-K1 cells viability dependence on EP buffers composition (No. 1, 2, 5, and 7) and applied protocols with pEGFP-N1 plasmid encoding green fluorescent protein (GFP). Dot line indicates transfection efficacy using 1.2 kV/cm × 100 μs × 8 protocol. CTRL refers to cells with plasmid in different buffer without electroporation treatment. Asterisk (*) corresponds to statistically significant differences ( p < 0.05).

    Article Snippet: Electroctroporation experiments were performed using a 3 kV, 100 ns–1 m square-wave pulse generator (VilniusTECH, Vilnius, Lithuania) ( ) and a commercially available electroporation cuvette with a 1 mm gap between electrodes (Biorad, Hercules, United States).

    Techniques: Plasmid Preparation, Transfection, Electroporation

    CHO-K1 (blue) and 4T1 (grey) normalized cell viability after electroporation with Luciferase-pcDNA3 plasmid. Both experiments were performed using No.1 EP buffer. Asterisk (*) corresponds to statistically significant ( p < 0.05) difference.

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Effects of buffer composition and plasmid toxicity on electroporation-based non-viral gene delivery in mammalian cells using bursts of nanosecond and microsecond pulses

    doi: 10.3389/fbioe.2024.1430637

    Figure Lengend Snippet: CHO-K1 (blue) and 4T1 (grey) normalized cell viability after electroporation with Luciferase-pcDNA3 plasmid. Both experiments were performed using No.1 EP buffer. Asterisk (*) corresponds to statistically significant ( p < 0.05) difference.

    Article Snippet: Electroctroporation experiments were performed using a 3 kV, 100 ns–1 m square-wave pulse generator (VilniusTECH, Vilnius, Lithuania) ( ) and a commercially available electroporation cuvette with a 1 mm gap between electrodes (Biorad, Hercules, United States).

    Techniques: Electroporation, Luciferase, Plasmid Preparation