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bio‐rad universal hood ii gel documentation system  (Bio-Rad)


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    Bio-Rad bio‐rad universal hood ii gel documentation system
    Bio‐Rad Universal Hood Ii Gel Documentation System, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bio+rad+universal+hood+ii+gel+documentation+system/Bio-Gel+P-2+Gel/pmc06093152-119-8-14
    Average 90 stars, based on 1 article reviews
    bio‐rad universal hood ii gel documentation system - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Polymerase Chain Reaction:

    Article Title: First report of histopathological and molecular characterizations of bovine herpesvirus-1 from outbreak at dairy farm in India
    Article Snippet: .. Horizontal gel electro-phoresis was conducted to determine the size of PCR products by 1.50% agarose gel, and the products were then visualized by Gel Documentation System (Universal Hood II; Bio-Rad, Hercules, USA). ..

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: Each reaction was performed in a final volume of 25 μL containing 1× PCR buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer (Macrogen, South Korea), 1.25 U of Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions included an initial denaturation at 94–95 °C for 5 min, followed by 30–35 cycles of denaturation at 94 °C for 30– 60 s, annealing at 44–60 °C for 1 min, and extension at 72 °C for 1 min, with a final extension at 72 °C for 7 min. PCR products were analysed by electrophoresis on a 2% agarose gel prepared in 1× TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: The PCR was performed in a total volume of 25 μL containing 1X reaction buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer, 1.25 U Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions consisted of an initial denaturation at 95 °C for 30 s, followed by 30 cycles of 95 °C for 30 s, 55 °C for 1 min, and 68 °C for 1 min 20 s, with a final extension at 68 °C for 10 min. PCR products were checked by electrophoresis on a 1% agarose gel prepared in 1X TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Agarose Gel Electrophoresis:

    Article Title: First report of histopathological and molecular characterizations of bovine herpesvirus-1 from outbreak at dairy farm in India
    Article Snippet: .. Horizontal gel electro-phoresis was conducted to determine the size of PCR products by 1.50% agarose gel, and the products were then visualized by Gel Documentation System (Universal Hood II; Bio-Rad, Hercules, USA). ..

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: Each reaction was performed in a final volume of 25 μL containing 1× PCR buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer (Macrogen, South Korea), 1.25 U of Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions included an initial denaturation at 94–95 °C for 5 min, followed by 30–35 cycles of denaturation at 94 °C for 30– 60 s, annealing at 44–60 °C for 1 min, and extension at 72 °C for 1 min, with a final extension at 72 °C for 7 min. PCR products were analysed by electrophoresis on a 2% agarose gel prepared in 1× TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: The PCR was performed in a total volume of 25 μL containing 1X reaction buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer, 1.25 U Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions consisted of an initial denaturation at 95 °C for 30 s, followed by 30 cycles of 95 °C for 30 s, 55 °C for 1 min, and 68 °C for 1 min 20 s, with a final extension at 68 °C for 10 min. PCR products were checked by electrophoresis on a 1% agarose gel prepared in 1X TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Article Title: Evaluation of bacteriophage cocktail on Urinary Tract Infection caused by colistin-resistant Klebsiella pneumoniae in mice model.
    Article Snippet: .. The agarose gel image was captured using a gel documentation system (BIO-RAD, Universal Hood II, USA). .. Whole genome sequencing of bacteriophage ΦKpnBHU1, ΦKpnBHU2, and ΦKpnBHU3 was done using NextSeq/ 2 × 150 Illumina sequencing technology at 100× coverage as described earlier [29].

    Hood:

    Article Title: First report of histopathological and molecular characterizations of bovine herpesvirus-1 from outbreak at dairy farm in India
    Article Snippet: .. Horizontal gel electro-phoresis was conducted to determine the size of PCR products by 1.50% agarose gel, and the products were then visualized by Gel Documentation System (Universal Hood II; Bio-Rad, Hercules, USA). ..

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: Each reaction was performed in a final volume of 25 μL containing 1× PCR buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer (Macrogen, South Korea), 1.25 U of Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions included an initial denaturation at 94–95 °C for 5 min, followed by 30–35 cycles of denaturation at 94 °C for 30– 60 s, annealing at 44–60 °C for 1 min, and extension at 72 °C for 1 min, with a final extension at 72 °C for 7 min. PCR products were analysed by electrophoresis on a 2% agarose gel prepared in 1× TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Article Title: Metformin instigates cellular autophagy to ameliorate high-fat diet-induced pancreatic inflammation and fibrosis/EMT in mice.
    Article Snippet: Background: Chronic pancreatic dysfunction is frequently observed as a consequence of prolonged high-fat diet consumption and is a serious public health concern.. This pro-diabetic insult aggravates inflammation-influenced fibrotic lesions and is associated with deregulated autophagy.. Metformin, a conventional anti-hyperglycemic drug, might be beneficial for pancreatic health, but the complex molecular regulations are not clarified.

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: The PCR was performed in a total volume of 25 μL containing 1X reaction buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer, 1.25 U Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions consisted of an initial denaturation at 95 °C for 30 s, followed by 30 cycles of 95 °C for 30 s, 55 °C for 1 min, and 68 °C for 1 min 20 s, with a final extension at 68 °C for 10 min. PCR products were checked by electrophoresis on a 1% agarose gel prepared in 1X TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Article Title: Molecular Characterisation of Escherichia coli Collected From an Urban River in Johannesburg, South Africa
    Article Snippet: .. The gels were visualised under UV transillumination, and electrophoretic images were captured using the Gel Doc EZ System (Universal Hood II Gel Doc System, Bio‐Rad, CA, USA). ..

    Article Title: Identification of protein aggregates in the aging vertebrate brain with prion-like and phase-separation properties.
    Article Snippet: In case of preparing purified recombinant protein inputs for the ATPase activity assay, we used dialysis exclusively to remove excess dye while adjusting the salt concentration to a desired level (50 mM NaCl) at the same time (Slide-A-Lyzer 20K MWCOMini dialysis cassette were used, Thermo Cat#69590). .. Successful labeling was verified by running SDS-PAGE and image the gel directly using Bio-Rad Universal Hood II Gel Doc Molecular Imaging System CFW-1212M (using the protein blot DyLight 550 setting, excitation/emission: 550/518). .. We ran a small amount (1 mL) of Bio-Rad Precision Plus Protein WesternC standards along with the labeled protein while keeping at least one open lane in between the protein ladder and sample to avoid signal bleed-through.

    Article Title: Evaluation of bacteriophage cocktail on Urinary Tract Infection caused by colistin-resistant Klebsiella pneumoniae in mice model.
    Article Snippet: .. The agarose gel image was captured using a gel documentation system (BIO-RAD, Universal Hood II, USA). .. Whole genome sequencing of bacteriophage ΦKpnBHU1, ΦKpnBHU2, and ΦKpnBHU3 was done using NextSeq/ 2 × 150 Illumina sequencing technology at 100× coverage as described earlier [29].

    Electrophoresis:

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: Each reaction was performed in a final volume of 25 μL containing 1× PCR buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer (Macrogen, South Korea), 1.25 U of Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions included an initial denaturation at 94–95 °C for 5 min, followed by 30–35 cycles of denaturation at 94 °C for 30– 60 s, annealing at 44–60 °C for 1 min, and extension at 72 °C for 1 min, with a final extension at 72 °C for 7 min. PCR products were analysed by electrophoresis on a 2% agarose gel prepared in 1× TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: The PCR was performed in a total volume of 25 μL containing 1X reaction buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer, 1.25 U Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions consisted of an initial denaturation at 95 °C for 30 s, followed by 30 cycles of 95 °C for 30 s, 55 °C for 1 min, and 68 °C for 1 min 20 s, with a final extension at 68 °C for 10 min. PCR products were checked by electrophoresis on a 1% agarose gel prepared in 1X TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Staining:

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: Each reaction was performed in a final volume of 25 μL containing 1× PCR buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer (Macrogen, South Korea), 1.25 U of Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions included an initial denaturation at 94–95 °C for 5 min, followed by 30–35 cycles of denaturation at 94 °C for 30– 60 s, annealing at 44–60 °C for 1 min, and extension at 72 °C for 1 min, with a final extension at 72 °C for 7 min. PCR products were analysed by electrophoresis on a 2% agarose gel prepared in 1× TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Article Title: Plant growth-promoting traits of Rhizophora mangle-associated bacteria and their effects on tomato (Solanum lycopersicum)
    Article Snippet: The PCR was performed in a total volume of 25 μL containing 1X reaction buffer (New England Biolabs, USA), 200 μM of each dNTP (New England Biolabs), 0.2 μM of each primer, 1.25 U Taq DNA polymerase (New England Biolabs), and ≤1 μg of template DNA. .. Thermal cycling conditions consisted of an initial denaturation at 95 °C for 30 s, followed by 30 cycles of 95 °C for 30 s, 55 °C for 1 min, and 68 °C for 1 min 20 s, with a final extension at 68 °C for 10 min. PCR products were checked by electrophoresis on a 1% agarose gel prepared in 1X TAE buffer, stained with GelRed (Biotium, USA), and visualised using a gel documentation system (Bio-Rad Universal Hood II). ..

    Membrane:

    Article Title: Metformin instigates cellular autophagy to ameliorate high-fat diet-induced pancreatic inflammation and fibrosis/EMT in mice.
    Article Snippet: Background: Chronic pancreatic dysfunction is frequently observed as a consequence of prolonged high-fat diet consumption and is a serious public health concern.. This pro-diabetic insult aggravates inflammation-influenced fibrotic lesions and is associated with deregulated autophagy.. Metformin, a conventional anti-hyperglycemic drug, might be beneficial for pancreatic health, but the complex molecular regulations are not clarified.

    Labeling:

    Article Title: Identification of protein aggregates in the aging vertebrate brain with prion-like and phase-separation properties.
    Article Snippet: In case of preparing purified recombinant protein inputs for the ATPase activity assay, we used dialysis exclusively to remove excess dye while adjusting the salt concentration to a desired level (50 mM NaCl) at the same time (Slide-A-Lyzer 20K MWCOMini dialysis cassette were used, Thermo Cat#69590). .. Successful labeling was verified by running SDS-PAGE and image the gel directly using Bio-Rad Universal Hood II Gel Doc Molecular Imaging System CFW-1212M (using the protein blot DyLight 550 setting, excitation/emission: 550/518). .. We ran a small amount (1 mL) of Bio-Rad Precision Plus Protein WesternC standards along with the labeled protein while keeping at least one open lane in between the protein ladder and sample to avoid signal bleed-through.

    SDS Page:

    Article Title: Identification of protein aggregates in the aging vertebrate brain with prion-like and phase-separation properties.
    Article Snippet: In case of preparing purified recombinant protein inputs for the ATPase activity assay, we used dialysis exclusively to remove excess dye while adjusting the salt concentration to a desired level (50 mM NaCl) at the same time (Slide-A-Lyzer 20K MWCOMini dialysis cassette were used, Thermo Cat#69590). .. Successful labeling was verified by running SDS-PAGE and image the gel directly using Bio-Rad Universal Hood II Gel Doc Molecular Imaging System CFW-1212M (using the protein blot DyLight 550 setting, excitation/emission: 550/518). .. We ran a small amount (1 mL) of Bio-Rad Precision Plus Protein WesternC standards along with the labeled protein while keeping at least one open lane in between the protein ladder and sample to avoid signal bleed-through.

    Imaging:

    Article Title: Identification of protein aggregates in the aging vertebrate brain with prion-like and phase-separation properties.
    Article Snippet: In case of preparing purified recombinant protein inputs for the ATPase activity assay, we used dialysis exclusively to remove excess dye while adjusting the salt concentration to a desired level (50 mM NaCl) at the same time (Slide-A-Lyzer 20K MWCOMini dialysis cassette were used, Thermo Cat#69590). .. Successful labeling was verified by running SDS-PAGE and image the gel directly using Bio-Rad Universal Hood II Gel Doc Molecular Imaging System CFW-1212M (using the protein blot DyLight 550 setting, excitation/emission: 550/518). .. We ran a small amount (1 mL) of Bio-Rad Precision Plus Protein WesternC standards along with the labeled protein while keeping at least one open lane in between the protein ladder and sample to avoid signal bleed-through.



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    Bio-Rad bio‐rad universal hood ii gel documentation system
    Bio‐Rad Universal Hood Ii Gel Documentation System, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bio+rad+universal+hood+ii+gel+documentation+system/Bio-Gel+P-2+Gel/pmc06093152-119-8-14
    Average 90 stars, based on 1 article reviews
    bio‐rad universal hood ii gel documentation system - by Bioz Stars, 2026-09
    90/100 stars
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