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gene pulser apparatus  (Bio-Rad)


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    Structured Review

    Bio-Rad gene pulser apparatus
    Gene Pulser Apparatus, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1942 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gene+pulser+electroporation+apparatus/Gene+Pulser+Electroporation+Buffer/10__1094_slash_phyto___07___25___0261___r-48-15-18
    Average 96 stars, based on 1942 article reviews
    gene pulser apparatus - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Electroporation:

    Article Title: Dual-function protein for lipid and blood glucose regulation
    Article Snippet: .. A Gene Pulser electroporation apparatus (Bio-Rad Laboratories, Hercules, CA) setting at 300 V of electric field and 1500 pFd of capacitance was used in the present experiment and 50 pg pure expression plasmid was mixed with 5×107 CHO cells in the cuvette. ..

    Article Title: Enhancing β-Carotene Production in Escherichia coli by Perturbing Central Carbon Metabolism and Improving the NADPH Supply.
    Article Snippet: .. The target DNA fragment was dispensed into 1-mm-gap cuvettes (Thermo Fisher Scientific, Waltham, MA, USA) containing Frontiers in Bioengineering and Biotechnology | www.frontiersin.org 3 June 2020 | Volume 8 | Article 585 pTKRED-carrying competent cells and electroporated into the cells at 1.8 kV, 25 μF, and 200 using a gene pulser electroporation apparatus (Bio-Rad, Hercules, CA, USA). ..

    Article Title: MEK1/2 regulate normal BCR and ABL1 tumor-suppressor functions to dictate ATO response in TKI-resistant Ph+ leukemia
    Article Snippet: Flow cytometry assay to evaluate Mitochondrial Transmembrane Potential (ΔΨm) was performed according to the manufacturer’s protocols (MitoLight®, Chemicon®). siRNA transfections Prior to electroporation, CML cells were washed twice with serum-free RPMI 1640 medium and resuspended in Opti-MEM (GibcoBRL, Grand Island, NY) to a final concentration of 24x106 cells/mL. .. Subsequently, 0.4 mL of cells suspension was mixed with 1 nmol of a smart pool small interfering double-stranded RNAs (siRNA) against TAp73, ΔNp73, MEK1/2 (manuscript, ref. 13-16) or nonspecific control siRNA obtained from Dharmacon Tech (Lafayette, Co) and electroporated in a 0.4- cm cuvette using the Gene Pulser electroporation apparatus (Bio-Rad Laboratories Inc, Herculex, California) using a single-pulse protocol (voltage 250 mV/capacitance 1050 μF). ..

    Article Title: Vaccine against infectious bronchitis virus
    Article Snippet: As infection of most IBV is not possible in continuous cell lines, IBV viral RNA was transfected into BHK-21 cells instead, a cell line known to support replication of the cell culture-adapted IBV strain Beaudette. .. Twenty microliters of IBV-H52 viral RNA, together with 10 μl transcript reaction mixtures of p-mIBV and p-IBV-N, were transfected into BHK-21 cells by electroporation using two pulses at 850V and 25 μF in a Gene Pulser electroporation apparatus (Bio-Rad). ..

    Article Title: Genetically modified yeast cell and improved process for production of clot-specific streptokinase
    Article Snippet: .. The cells were transformed with the linearized DNA using a gene-pulser electroporation apparatus (Biorad) at the settings of 1.5 KV, 25 μF with 200Ω resistance and 1 ml of ice-cold 1 M sorbitol was immediately added to the cuvette as described in the Invitrogen users manual. ..

    Article Title: Improvement of the dP-nucleoside-mediated herpes simplex virus thymidine kinase negative-selection system by manipulating dP metabolism genes.
    Article Snippet: Please cite selection sy A variety of positive/negative selection systems have been exploited as genome engineering tools and screening platforms for genetic switches.. While numerous positive-selection systems are available, only a handful of negativeselection systems are useful for such applications.. We previously reported a powerful negative-selection system using herpes simplex virus thymidine kinase (HsvTK) and the mutagenic nucleoside analog 6-(b-D-2-deoxyribofuranosyl)-3,4dihydro-8H-pyrimido [4,5-c][1,2] oxazin-7-one (dP).

    Article Title: Development of novel reagents to chicken FLT3, XCR1 and CSF2R for the identification and characterization of avian conventional dendritic cells
    Article Snippet: .. The cuvettes were left to equilibrate at room temperature (RT) for 10 min before electroporation at 975 μF and 300 V using a Bio‐Rad Gene Pulser electroporation apparatus. .. After electroporation, cells were washed in complete medium to remove surplus DNA, plated out in 6‐well plates and then incubated at 37 oC for 24 h before adding 40 μg/ml blasticidin (Fisher Bioreagents, Fisher Scientific) for three weeks.

    Article Title: Enhancing β-Carotene Production in Escherichia coli by Perturbing Central Carbon Metabolism and Improving the NADPH Supply
    Article Snippet: .. The target DNA fragment was dispensed into 1-mm-gap cuvettes (Thermo Fisher Scientific, Waltham, MA, USA) containing pTKRED-carrying competent cells and electroporated into the cells at 1.8 kV, 25 μF, and 200 Ω using a gene pulser electroporation apparatus (Bio-Rad, Hercules, CA, USA). ..

    Expressing:

    Article Title: Dual-function protein for lipid and blood glucose regulation
    Article Snippet: .. A Gene Pulser electroporation apparatus (Bio-Rad Laboratories, Hercules, CA) setting at 300 V of electric field and 1500 pFd of capacitance was used in the present experiment and 50 pg pure expression plasmid was mixed with 5×107 CHO cells in the cuvette. ..

    Plasmid Preparation:

    Article Title: Dual-function protein for lipid and blood glucose regulation
    Article Snippet: .. A Gene Pulser electroporation apparatus (Bio-Rad Laboratories, Hercules, CA) setting at 300 V of electric field and 1500 pFd of capacitance was used in the present experiment and 50 pg pure expression plasmid was mixed with 5×107 CHO cells in the cuvette. ..

    Suspension:

    Article Title: MEK1/2 regulate normal BCR and ABL1 tumor-suppressor functions to dictate ATO response in TKI-resistant Ph+ leukemia
    Article Snippet: Flow cytometry assay to evaluate Mitochondrial Transmembrane Potential (ΔΨm) was performed according to the manufacturer’s protocols (MitoLight®, Chemicon®). siRNA transfections Prior to electroporation, CML cells were washed twice with serum-free RPMI 1640 medium and resuspended in Opti-MEM (GibcoBRL, Grand Island, NY) to a final concentration of 24x106 cells/mL. .. Subsequently, 0.4 mL of cells suspension was mixed with 1 nmol of a smart pool small interfering double-stranded RNAs (siRNA) against TAp73, ΔNp73, MEK1/2 (manuscript, ref. 13-16) or nonspecific control siRNA obtained from Dharmacon Tech (Lafayette, Co) and electroporated in a 0.4- cm cuvette using the Gene Pulser electroporation apparatus (Bio-Rad Laboratories Inc, Herculex, California) using a single-pulse protocol (voltage 250 mV/capacitance 1050 μF). ..

    Control:

    Article Title: MEK1/2 regulate normal BCR and ABL1 tumor-suppressor functions to dictate ATO response in TKI-resistant Ph+ leukemia
    Article Snippet: Flow cytometry assay to evaluate Mitochondrial Transmembrane Potential (ΔΨm) was performed according to the manufacturer’s protocols (MitoLight®, Chemicon®). siRNA transfections Prior to electroporation, CML cells were washed twice with serum-free RPMI 1640 medium and resuspended in Opti-MEM (GibcoBRL, Grand Island, NY) to a final concentration of 24x106 cells/mL. .. Subsequently, 0.4 mL of cells suspension was mixed with 1 nmol of a smart pool small interfering double-stranded RNAs (siRNA) against TAp73, ΔNp73, MEK1/2 (manuscript, ref. 13-16) or nonspecific control siRNA obtained from Dharmacon Tech (Lafayette, Co) and electroporated in a 0.4- cm cuvette using the Gene Pulser electroporation apparatus (Bio-Rad Laboratories Inc, Herculex, California) using a single-pulse protocol (voltage 250 mV/capacitance 1050 μF). ..

    Transfection:

    Article Title: Vaccine against infectious bronchitis virus
    Article Snippet: As infection of most IBV is not possible in continuous cell lines, IBV viral RNA was transfected into BHK-21 cells instead, a cell line known to support replication of the cell culture-adapted IBV strain Beaudette. .. Twenty microliters of IBV-H52 viral RNA, together with 10 μl transcript reaction mixtures of p-mIBV and p-IBV-N, were transfected into BHK-21 cells by electroporation using two pulses at 850V and 25 μF in a Gene Pulser electroporation apparatus (Bio-Rad). ..

    Transformation Assay:

    Article Title: Genetically modified yeast cell and improved process for production of clot-specific streptokinase
    Article Snippet: .. The cells were transformed with the linearized DNA using a gene-pulser electroporation apparatus (Biorad) at the settings of 1.5 KV, 25 μF with 200Ω resistance and 1 ml of ice-cold 1 M sorbitol was immediately added to the cuvette as described in the Invitrogen users manual. ..

    Purification:

    Article Title: Improvement of the dP-nucleoside-mediated herpes simplex virus thymidine kinase negative-selection system by manipulating dP metabolism genes.
    Article Snippet: Please cite selection sy A variety of positive/negative selection systems have been exploited as genome engineering tools and screening platforms for genetic switches.. While numerous positive-selection systems are available, only a handful of negativeselection systems are useful for such applications.. We previously reported a powerful negative-selection system using herpes simplex virus thymidine kinase (HsvTK) and the mutagenic nucleoside analog 6-(b-D-2-deoxyribofuranosyl)-3,4dihydro-8H-pyrimido [4,5-c][1,2] oxazin-7-one (dP).

    Polymerase Chain Reaction:

    Article Title: Improvement of the dP-nucleoside-mediated herpes simplex virus thymidine kinase negative-selection system by manipulating dP metabolism genes.
    Article Snippet: Please cite selection sy A variety of positive/negative selection systems have been exploited as genome engineering tools and screening platforms for genetic switches.. While numerous positive-selection systems are available, only a handful of negativeselection systems are useful for such applications.. We previously reported a powerful negative-selection system using herpes simplex virus thymidine kinase (HsvTK) and the mutagenic nucleoside analog 6-(b-D-2-deoxyribofuranosyl)-3,4dihydro-8H-pyrimido [4,5-c][1,2] oxazin-7-one (dP).



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