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electroporation cuvette  (Bio-Rad)


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    Bio-Rad electroporation cuvette
    Electroporation Cuvette, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 718 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/electroporation+cuvette/Gene+Pulser+%2FMicroPulser+Electroporation+Cuvettes/pm42838434-48-32-34
    Average 96 stars, based on 718 article reviews
    electroporation cuvette - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Electroporation:

    Article Title: Genome-wide screening reveals producer-cell modifications that improve virus-like particle production and delivery potency
    Article Snippet: First, electrocompetent cells were generated from NEB ® Stable (New England Biolabs; C3040H) chemically competent E. coli by growing single colonies to mid-log phase in LB media containing 10 μg/mL tetracycline and 50 μg/mL streptomycin, collecting cells by centrifugation at 5000 × g for 1 min at 4 °C, washing with cold 10% (v/v) glycerol, and repeating for a total of four washes. .. Freshly prepared electrocompetent cells were transferred to a chilled 0.1 cm electroporation cuvette (Bio-Rad; 1652089) and mixed with the purified, assembled library plasmids. ..

    Article Title: Integrating design-of-experiments (DOE) optimization and risk assessment towards a safe and simplified electroporation protocol for Toxoplasma gondii
    Article Snippet: All electroporation experiments were performed on a Biorad Gene Pulser (Biorad 165–2076) with modified parameters described previously [ ]. .. Briefly, required number of tachyzoites released by shearing infected cells with a 27G blunt needle were resuspended in 150 μl pre-chilled electroporation buffer, mixed with pTub:dYFPpSAG1:CAT and transferred to a 0.4 cm electroporation cuvette (Biorad 1652088) on ice [ ]. ..

    Article Title: Utilization of a CRISPRi-based ex vivo challenge model to reveal temporally dependent gene essentiality in intracellular Mycobacterium tuberculosis .
    Article Snippet: .. The cells:DNA mix was transferred to a 2 mm electroporation cuvette (Bio-Rad #1652082) and electroporated at 2,500 kV, 700 ohms, and 25 μF. .. Each transformation was recovered in 5 mL 7H9 media supplemented with OADC, glycerol, and Tween 80 for 16–24 h. The recovered cells were harvested at 4,000 rpm for 10 min, resuspended in 1 mL remaining media per transformation, and plated on 7H10 agar supplemented with OADC, glycerol, Tween 80, and kanamycin in Corning Bioassay dishes (Sigma #CLS431111-16EA).

    Article Title: Utilization of a CRISPRi-based ex vivo challenge model to reveal temporally dependent gene essentiality in intracellular Mycobacterium tuberculosis .
    Article Snippet: .. For each transformation, 75 μL of the cells:DNA mix was transferred to a 0.1 cm electroporation cuvette (BioRad #1652089) and electroporated at 2,000 V, 200 ohms, and 25 μF. ..

    Article Title: Genome-wide screening reveals producer-cell modifications that improve virus-like particle production and delivery potency.
    Article Snippet: First, electrocompetent cells were generated from NEB® Stable (New England Biolabs; C3040H) chemically competent E. coli by growing single colonies to mid-log phase in LB media containing 10 μg/mL tetracycline and 50 μg/mL streptomycin, collecting cells by centrifugation at 5000× g for 1min at 4 °C, washing with cold 10% (v/v) glycerol, and repeating for a total of fourwashes. .. Freshly prepared electrocompetent cells were transferred to a chilled 0.1 cm electroporation cuvette (Bio-Rad; 1652089) and mixed with the purified, assembled library plasmids. ..

    Article Title: Lipid droplet-associated proteins integrate lipid metabolism, cell cycle, and cytoskeletal remodeling in colon cancer.
    Article Snippet: .. siRNA Transfection Colon cancer cells were diluted to a concentration of 5×106 cells/ml in Gene Pulser Electroporation Buffer (Bio-Rad, 1652677), 400 μl of this suspension was then transferred to a 0.4 cm electroporation cuvette (Bio-Rad, 1652081). .. Cells were then transfected with siRNA targeting ACSL4, PRR11, LASP1, MICAL2 (20 nM, Dharmacon J-009364-050005, J-007019-19-0005, J-010519-10-0005, J-010189-05-0005), non-targeting scrambled siRNA control (20 nM, Dharmacon D-001810-10-05), or electroporation buffer alone (negative control).

    Article Title: Isolation and biocontrol potential of the indigenous endophyte Bacillus amyloliquefaciens XJYM-Y9 from oat leaves against oat anthracnose
    Article Snippet: The plasmid pGFP4412 [58] was extracted using a TIANprep Mini Plasmid Kit (Tiangen, China) and quantified via a NanoDrop One spectrophotometer. .. For the transformation, 70 μL of competent cells were mixed with 7 μL of plasmid DNA in a pre-chilled 0.1 cm electroporation cuvette (Bio-Rad, USA) and incubation on ice for 20 min. Electroporation was performed using a MicroPulser electroporator (Bio-Rad, USA) under optimized parameters (20.5 kV/cm, 200 Ω, 5–6 ms. ..

    Purification:

    Article Title: Genome-wide screening reveals producer-cell modifications that improve virus-like particle production and delivery potency
    Article Snippet: First, electrocompetent cells were generated from NEB ® Stable (New England Biolabs; C3040H) chemically competent E. coli by growing single colonies to mid-log phase in LB media containing 10 μg/mL tetracycline and 50 μg/mL streptomycin, collecting cells by centrifugation at 5000 × g for 1 min at 4 °C, washing with cold 10% (v/v) glycerol, and repeating for a total of four washes. .. Freshly prepared electrocompetent cells were transferred to a chilled 0.1 cm electroporation cuvette (Bio-Rad; 1652089) and mixed with the purified, assembled library plasmids. ..

    Article Title: Genome-wide screening reveals producer-cell modifications that improve virus-like particle production and delivery potency.
    Article Snippet: First, electrocompetent cells were generated from NEB® Stable (New England Biolabs; C3040H) chemically competent E. coli by growing single colonies to mid-log phase in LB media containing 10 μg/mL tetracycline and 50 μg/mL streptomycin, collecting cells by centrifugation at 5000× g for 1min at 4 °C, washing with cold 10% (v/v) glycerol, and repeating for a total of fourwashes. .. Freshly prepared electrocompetent cells were transferred to a chilled 0.1 cm electroporation cuvette (Bio-Rad; 1652089) and mixed with the purified, assembled library plasmids. ..

    Infection:

    Article Title: Integrating design-of-experiments (DOE) optimization and risk assessment towards a safe and simplified electroporation protocol for Toxoplasma gondii
    Article Snippet: All electroporation experiments were performed on a Biorad Gene Pulser (Biorad 165–2076) with modified parameters described previously [ ]. .. Briefly, required number of tachyzoites released by shearing infected cells with a 27G blunt needle were resuspended in 150 μl pre-chilled electroporation buffer, mixed with pTub:dYFPpSAG1:CAT and transferred to a 0.4 cm electroporation cuvette (Biorad 1652088) on ice [ ]. ..

    Transformation Assay:

    Article Title: Utilization of a CRISPRi-based ex vivo challenge model to reveal temporally dependent gene essentiality in intracellular Mycobacterium tuberculosis .
    Article Snippet: .. For each transformation, 75 μL of the cells:DNA mix was transferred to a 0.1 cm electroporation cuvette (BioRad #1652089) and electroporated at 2,000 V, 200 ohms, and 25 μF. ..

    Article Title: Isolation and biocontrol potential of the indigenous endophyte Bacillus amyloliquefaciens XJYM-Y9 from oat leaves against oat anthracnose
    Article Snippet: The plasmid pGFP4412 [58] was extracted using a TIANprep Mini Plasmid Kit (Tiangen, China) and quantified via a NanoDrop One spectrophotometer. .. For the transformation, 70 μL of competent cells were mixed with 7 μL of plasmid DNA in a pre-chilled 0.1 cm electroporation cuvette (Bio-Rad, USA) and incubation on ice for 20 min. Electroporation was performed using a MicroPulser electroporator (Bio-Rad, USA) under optimized parameters (20.5 kV/cm, 200 Ω, 5–6 ms. ..

    other:

    Article Title: Utilization of a CRISPRi-based ex vivo challenge model to reveal temporally dependent gene essentiality in intracellular Mycobacterium tuberculosis
    Article Snippet: Each 20 μL Golden Gate reaction (six reactions for each sublibrary) contained 800 fmol of PCR amplicon, 80 fmol of BsmBI-digested plRL2, 20 mM DTT, 20 mM ATP, 1× FastDigest Buffer, 10 U of FastDigest Esp3I (Thermo Scientific #FD0454) and 1,000 units T4 DNA ligase (NEB #M0202M).

    Transfection:

    Article Title: Lipid droplet-associated proteins integrate lipid metabolism, cell cycle, and cytoskeletal remodeling in colon cancer.
    Article Snippet: .. siRNA Transfection Colon cancer cells were diluted to a concentration of 5×106 cells/ml in Gene Pulser Electroporation Buffer (Bio-Rad, 1652677), 400 μl of this suspension was then transferred to a 0.4 cm electroporation cuvette (Bio-Rad, 1652081). .. Cells were then transfected with siRNA targeting ACSL4, PRR11, LASP1, MICAL2 (20 nM, Dharmacon J-009364-050005, J-007019-19-0005, J-010519-10-0005, J-010189-05-0005), non-targeting scrambled siRNA control (20 nM, Dharmacon D-001810-10-05), or electroporation buffer alone (negative control).

    Concentration Assay:

    Article Title: Lipid droplet-associated proteins integrate lipid metabolism, cell cycle, and cytoskeletal remodeling in colon cancer.
    Article Snippet: .. siRNA Transfection Colon cancer cells were diluted to a concentration of 5×106 cells/ml in Gene Pulser Electroporation Buffer (Bio-Rad, 1652677), 400 μl of this suspension was then transferred to a 0.4 cm electroporation cuvette (Bio-Rad, 1652081). .. Cells were then transfected with siRNA targeting ACSL4, PRR11, LASP1, MICAL2 (20 nM, Dharmacon J-009364-050005, J-007019-19-0005, J-010519-10-0005, J-010189-05-0005), non-targeting scrambled siRNA control (20 nM, Dharmacon D-001810-10-05), or electroporation buffer alone (negative control).

    Suspension:

    Article Title: Lipid droplet-associated proteins integrate lipid metabolism, cell cycle, and cytoskeletal remodeling in colon cancer.
    Article Snippet: .. siRNA Transfection Colon cancer cells were diluted to a concentration of 5×106 cells/ml in Gene Pulser Electroporation Buffer (Bio-Rad, 1652677), 400 μl of this suspension was then transferred to a 0.4 cm electroporation cuvette (Bio-Rad, 1652081). .. Cells were then transfected with siRNA targeting ACSL4, PRR11, LASP1, MICAL2 (20 nM, Dharmacon J-009364-050005, J-007019-19-0005, J-010519-10-0005, J-010189-05-0005), non-targeting scrambled siRNA control (20 nM, Dharmacon D-001810-10-05), or electroporation buffer alone (negative control).

    Plasmid Preparation:

    Article Title: Isolation and biocontrol potential of the indigenous endophyte Bacillus amyloliquefaciens XJYM-Y9 from oat leaves against oat anthracnose
    Article Snippet: The plasmid pGFP4412 [58] was extracted using a TIANprep Mini Plasmid Kit (Tiangen, China) and quantified via a NanoDrop One spectrophotometer. .. For the transformation, 70 μL of competent cells were mixed with 7 μL of plasmid DNA in a pre-chilled 0.1 cm electroporation cuvette (Bio-Rad, USA) and incubation on ice for 20 min. Electroporation was performed using a MicroPulser electroporator (Bio-Rad, USA) under optimized parameters (20.5 kV/cm, 200 Ω, 5–6 ms. ..

    Incubation:

    Article Title: Isolation and biocontrol potential of the indigenous endophyte Bacillus amyloliquefaciens XJYM-Y9 from oat leaves against oat anthracnose
    Article Snippet: The plasmid pGFP4412 [58] was extracted using a TIANprep Mini Plasmid Kit (Tiangen, China) and quantified via a NanoDrop One spectrophotometer. .. For the transformation, 70 μL of competent cells were mixed with 7 μL of plasmid DNA in a pre-chilled 0.1 cm electroporation cuvette (Bio-Rad, USA) and incubation on ice for 20 min. Electroporation was performed using a MicroPulser electroporator (Bio-Rad, USA) under optimized parameters (20.5 kV/cm, 200 Ω, 5–6 ms. ..



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