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bio rad gene pulser xcell electroporation system  (Bio-Rad)


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    Bio-Rad bio rad gene pulser xcell electroporation system
    Bio Rad Gene Pulser Xcell Electroporation System, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 97/100, based on 5935 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gene+pulser+electroporation+system/Gene+Pulser+Xcell+Total+System/pmc12811641-358-13-13
    Average 97 stars, based on 5935 article reviews
    bio rad gene pulser xcell electroporation system - by Bioz Stars, 2026-10
    97/100 stars

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    Related Articles

    Negative Control:

    Article Title: Improvement of carboplatin chemosensitivity in lung cancer cells by siRNA-mediated downregulation of DLGAP1-AS2 expression
    Article Snippet: .. To optimize the dosage of siRNA, scramble siRNA (negative control, 5’ UUCUCCGAACGUGUCACGUUU 3’) and siRNA-DLGAP1-AS2 (Table ) were transfected separately into A549 cells at varying doses (10, 20, and 40 pmol) using a gene pulser electroporation system (BioRad). ..

    Article Title: Improvement of carboplatin chemosensitivity in lung cancer cells by siRNA-mediated downregulation of DLGAP1-AS2 expression.
    Article Snippet: To detach the cells, 0.25% Trypsin/EDTA from Gibco was used, and trypsin activity was subsequently neutralized in complete medium containing 10% FBS. .. After being subcultured three times to achieve the logarithmic growth phase, characterized by clear cell morphology and stable cell function, the cell lines were ready for further experimentation. siRNA transfection To optimize the dosage of siRNA, scramble siRNA (negative control, 5’ U U C U C C G A A C G U G U C A C G U U U 3’) and siRNA-DLGAP1-AS2 (Table 1) were transfected separately into A549 cells at varying doses (10, 20, and 40 pmol) using a gene pulser electroporation system (BioRad). ..

    Transfection:

    Article Title: Improvement of carboplatin chemosensitivity in lung cancer cells by siRNA-mediated downregulation of DLGAP1-AS2 expression
    Article Snippet: .. To optimize the dosage of siRNA, scramble siRNA (negative control, 5’ UUCUCCGAACGUGUCACGUUU 3’) and siRNA-DLGAP1-AS2 (Table ) were transfected separately into A549 cells at varying doses (10, 20, and 40 pmol) using a gene pulser electroporation system (BioRad). ..

    Article Title: Improvement of carboplatin chemosensitivity in lung cancer cells by siRNA-mediated downregulation of DLGAP1-AS2 expression.
    Article Snippet: To detach the cells, 0.25% Trypsin/EDTA from Gibco was used, and trypsin activity was subsequently neutralized in complete medium containing 10% FBS. .. After being subcultured three times to achieve the logarithmic growth phase, characterized by clear cell morphology and stable cell function, the cell lines were ready for further experimentation. siRNA transfection To optimize the dosage of siRNA, scramble siRNA (negative control, 5’ U U C U C C G A A C G U G U C A C G U U U 3’) and siRNA-DLGAP1-AS2 (Table 1) were transfected separately into A549 cells at varying doses (10, 20, and 40 pmol) using a gene pulser electroporation system (BioRad). ..

    Article Title: Immediate early splicing controls translation in activated T-cells and is mediated by hnRNPC2 phosphorylation
    Article Snippet: Transfections of HEK293 and HeLa cells using either ROTIFect (Carl Roth) or Lipofectamine 2000, respectively were performed according to the manufacturer’s instructions. .. Transfections of Jurkat cells were performed using a Gene Pulser electroporation system (Bio-Rad) for morpholino experiments and Nucleofector II from Amaxa Biosystems for siRNAs transfections. ..

    Electroporation:

    Article Title: Improvement of carboplatin chemosensitivity in lung cancer cells by siRNA-mediated downregulation of DLGAP1-AS2 expression
    Article Snippet: .. To optimize the dosage of siRNA, scramble siRNA (negative control, 5’ UUCUCCGAACGUGUCACGUUU 3’) and siRNA-DLGAP1-AS2 (Table ) were transfected separately into A549 cells at varying doses (10, 20, and 40 pmol) using a gene pulser electroporation system (BioRad). ..

    Article Title: Heterogeneity of iridoid biosynthesis in catmints: Molecular background in a phylogenetic context
    Article Snippet: .. Agrobacterium tumefaciens strain LBA4404 was transformed with 300 ng of plasmid DNA using the electroporation method with the Gene Pulser Electroporation System (Bio‐Rad, Hercules, CA, USA). ..

    Article Title: The role of PD-L1 gene silencing on growth, migration, and apoptosis in oral squamous carcinoma cell line HN-5
    Article Snippet: .. A Gene Pulser Electroporation System (Bio-Rad) was utilized for electroporation at a time constant of 12.5 ms and a voltage of 160 V. After transferring the cells into a 6-well plate with RPMI-1640 media containing 10% FBS, they were incubated for 24 hours at a temperature of 37°C. ..

    Article Title: Improvement of carboplatin chemosensitivity in lung cancer cells by siRNA-mediated downregulation of DLGAP1-AS2 expression.
    Article Snippet: To detach the cells, 0.25% Trypsin/EDTA from Gibco was used, and trypsin activity was subsequently neutralized in complete medium containing 10% FBS. .. After being subcultured three times to achieve the logarithmic growth phase, characterized by clear cell morphology and stable cell function, the cell lines were ready for further experimentation. siRNA transfection To optimize the dosage of siRNA, scramble siRNA (negative control, 5’ U U C U C C G A A C G U G U C A C G U U U 3’) and siRNA-DLGAP1-AS2 (Table 1) were transfected separately into A549 cells at varying doses (10, 20, and 40 pmol) using a gene pulser electroporation system (BioRad). ..

    Article Title: Plasticity in a bacterial global regulatory switch that drives a shift in antibiotic resistance and virulence
    Article Snippet: .. Electrocompetent PA cells were prepared by washing in 300 mM sucrose and transformation with the constructs was performed using a Gene Pulser Electroporation System (Bio-Rad, U.S.A.) with the following settings: 200 Ω, 2.5 kV before plating onto sucrose agar to counter select the plasmid. .. Colonies with the insert were then confirmed by sequencing (Eurofins Scientific, Luxembourg) and thereafter named PAΔ.

    Article Title: Immediate early splicing controls translation in activated T-cells and is mediated by hnRNPC2 phosphorylation
    Article Snippet: Transfections of HEK293 and HeLa cells using either ROTIFect (Carl Roth) or Lipofectamine 2000, respectively were performed according to the manufacturer’s instructions. .. Transfections of Jurkat cells were performed using a Gene Pulser electroporation system (Bio-Rad) for morpholino experiments and Nucleofector II from Amaxa Biosystems for siRNAs transfections. ..

    other:

    Article Title: Immediate early splicing controls translation in activated T-cells and is mediated by hnRNPC2 phosphorylation.
    Article Snippet: Events were then clustered into bins centred between −0.15 and −0.65 (in 0.05 steps) using GraphPad Prism.

    Article Title: Heterogeneity of iridoid biosynthesis in catmints: Molecular background in a phylogenetic context.
    Article Snippet: Reconstitution of nepetalactone production in chemotype B N. grandiflora leaves Cloning Coding sequences for NrNEPS1, identified in the N. rtanjensis transcriptome (Aničić et al., 2020), and NcNEPS5 from N. cataria (Lichman et al., 2020) were assembled into expression constructs using the Modular Cloning (MoClo) toolkit (Addgene, Watertown, MA, USA) and the Plant MoClo toolkit (Weber et al., 2011; Engler et al., 2014).

    Transformation Assay:

    Article Title: Heterogeneity of iridoid biosynthesis in catmints: Molecular background in a phylogenetic context
    Article Snippet: .. Agrobacterium tumefaciens strain LBA4404 was transformed with 300 ng of plasmid DNA using the electroporation method with the Gene Pulser Electroporation System (Bio‐Rad, Hercules, CA, USA). ..

    Article Title: Plasticity in a bacterial global regulatory switch that drives a shift in antibiotic resistance and virulence
    Article Snippet: .. Electrocompetent PA cells were prepared by washing in 300 mM sucrose and transformation with the constructs was performed using a Gene Pulser Electroporation System (Bio-Rad, U.S.A.) with the following settings: 200 Ω, 2.5 kV before plating onto sucrose agar to counter select the plasmid. .. Colonies with the insert were then confirmed by sequencing (Eurofins Scientific, Luxembourg) and thereafter named PAΔ.

    Plasmid Preparation:

    Article Title: Heterogeneity of iridoid biosynthesis in catmints: Molecular background in a phylogenetic context
    Article Snippet: .. Agrobacterium tumefaciens strain LBA4404 was transformed with 300 ng of plasmid DNA using the electroporation method with the Gene Pulser Electroporation System (Bio‐Rad, Hercules, CA, USA). ..

    Article Title: Plasticity in a bacterial global regulatory switch that drives a shift in antibiotic resistance and virulence
    Article Snippet: .. Electrocompetent PA cells were prepared by washing in 300 mM sucrose and transformation with the constructs was performed using a Gene Pulser Electroporation System (Bio-Rad, U.S.A.) with the following settings: 200 Ω, 2.5 kV before plating onto sucrose agar to counter select the plasmid. .. Colonies with the insert were then confirmed by sequencing (Eurofins Scientific, Luxembourg) and thereafter named PAΔ.

    Transferring:

    Article Title: The role of PD-L1 gene silencing on growth, migration, and apoptosis in oral squamous carcinoma cell line HN-5
    Article Snippet: .. A Gene Pulser Electroporation System (Bio-Rad) was utilized for electroporation at a time constant of 12.5 ms and a voltage of 160 V. After transferring the cells into a 6-well plate with RPMI-1640 media containing 10% FBS, they were incubated for 24 hours at a temperature of 37°C. ..

    Incubation:

    Article Title: The role of PD-L1 gene silencing on growth, migration, and apoptosis in oral squamous carcinoma cell line HN-5
    Article Snippet: .. A Gene Pulser Electroporation System (Bio-Rad) was utilized for electroporation at a time constant of 12.5 ms and a voltage of 160 V. After transferring the cells into a 6-well plate with RPMI-1640 media containing 10% FBS, they were incubated for 24 hours at a temperature of 37°C. ..

    Stable Transfection:

    Article Title: Improvement of carboplatin chemosensitivity in lung cancer cells by siRNA-mediated downregulation of DLGAP1-AS2 expression.
    Article Snippet: To detach the cells, 0.25% Trypsin/EDTA from Gibco was used, and trypsin activity was subsequently neutralized in complete medium containing 10% FBS. .. After being subcultured three times to achieve the logarithmic growth phase, characterized by clear cell morphology and stable cell function, the cell lines were ready for further experimentation. siRNA transfection To optimize the dosage of siRNA, scramble siRNA (negative control, 5’ U U C U C C G A A C G U G U C A C G U U U 3’) and siRNA-DLGAP1-AS2 (Table 1) were transfected separately into A549 cells at varying doses (10, 20, and 40 pmol) using a gene pulser electroporation system (BioRad). ..

    Construct:

    Article Title: Plasticity in a bacterial global regulatory switch that drives a shift in antibiotic resistance and virulence
    Article Snippet: .. Electrocompetent PA cells were prepared by washing in 300 mM sucrose and transformation with the constructs was performed using a Gene Pulser Electroporation System (Bio-Rad, U.S.A.) with the following settings: 200 Ω, 2.5 kV before plating onto sucrose agar to counter select the plasmid. .. Colonies with the insert were then confirmed by sequencing (Eurofins Scientific, Luxembourg) and thereafter named PAΔ.



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    Image Search Results


    Schematic illustration of the preparation of M2-exo@HI and its mediated therapeutic mechanisms and signaling pathways. (a) RAW264.7 macrophages were polarized to M2 phenotype using DEX, followed by M2-exo isolation from cell supernatant via differential centrifugation. M2-exo@HI was prepared through encapsulating HI into M2-exo by electroporation. (b) M2-exo@HI crossed the BBB and localized to microglia in the hemorrhagic brain, delivering the HI plasmid into the nucleus. This prompted expression and secretion of Hp and IL-10 by microglia. The released Hp inhibited Hb toxicity by binding to Hb. IL-10 shifted microglial polarization from the pro-inflammatory M1 phenotype toward the reparative M2 phenotype, removing hematoma by engulfing erythrocyte and Hb-Hp complex, and decreasing pro-inflammatory cytokine levels—collectively enhancing neuroprotection and BBB repair. These beneficial outcomes were linked to the inhibition of the IL-17 and NF-κB signaling pathways and activation of the PI3K-Akt and ferroptosis pathways.

    Journal: Bioactive Materials

    Article Title: M2 macrophage-derived exosomes delivering haptoglobin and interleukin-10 plasmids for synergistic therapy of intracerebral hemorrhage

    doi: 10.1016/j.bioactmat.2026.01.047

    Figure Lengend Snippet: Schematic illustration of the preparation of M2-exo@HI and its mediated therapeutic mechanisms and signaling pathways. (a) RAW264.7 macrophages were polarized to M2 phenotype using DEX, followed by M2-exo isolation from cell supernatant via differential centrifugation. M2-exo@HI was prepared through encapsulating HI into M2-exo by electroporation. (b) M2-exo@HI crossed the BBB and localized to microglia in the hemorrhagic brain, delivering the HI plasmid into the nucleus. This prompted expression and secretion of Hp and IL-10 by microglia. The released Hp inhibited Hb toxicity by binding to Hb. IL-10 shifted microglial polarization from the pro-inflammatory M1 phenotype toward the reparative M2 phenotype, removing hematoma by engulfing erythrocyte and Hb-Hp complex, and decreasing pro-inflammatory cytokine levels—collectively enhancing neuroprotection and BBB repair. These beneficial outcomes were linked to the inhibition of the IL-17 and NF-κB signaling pathways and activation of the PI3K-Akt and ferroptosis pathways.

    Article Snippet: M2-exo (100 μL, 1 mg/mL), HI plasmid (circular pBudCE4.1, 100 μg, TsingkeBiotechnology., Ltd.), and 100 μL PBS were added to the electroporation cuvettes (Bio-Rad 165-2088).

    Techniques: Protein-Protein interactions, Isolation, Centrifugation, Electroporation, Plasmid Preparation, Expressing, Binding Assay, Inhibition, Activation Assay