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custom designed sybr plate  (Bio-Rad)


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    Structured Review

    Bio-Rad custom designed sybr plate
    Custom Designed Sybr Plate, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 217 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/custom-designed+software/PrimePCR+Analysis+Software/pm40646626-121-64-67
    Average 99 stars, based on 217 article reviews
    custom designed sybr plate - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Isothermal and protein-free cascade catalytic hairpin assembly induced-DNAzyme sensing strategy for sensitive miRNA analysis
    Article Snippet: Electrophoresis was performed using a gel electrophoresis unit (Bio-Rad Laboratories, USA) submerged in 1× TBE running buffer (89 mM Tris-borate, 2 mM EDTA, pH 8.3). .. Separation was carried out at a constant voltage of 80 V for 70 min. Post-electrophoresis, the gel was immersed in a diluted solution of Super GelRedTM nucleic acid stain for 20 min. Gel images were subsequently captured and documented using a Gel DocTM EZ system equipped with Image LabTM imaging and analysis software (Bio-Rad Laboratories, USA). ..

    Article Title: Isothermal and protein-free cascade catalytic hairpin assembly induced-DNAzyme sensing strategy for sensitive miRNA analysis.
    Article Snippet: Electrophoresis was performed using a gel electrophoresis unit (Bio-Rad Laboratories, USA) submerged in 1× TBE running buffer (89 mM Tris-borate, 2 mM EDTA, pH 8.3). .. Separation was carried out at a constant voltage of 80 V for 70 min. Post-electrophoresis, the gel was immersed in a diluted solution of Super GelRedTM nucleic acid stain for 20 min. Gel images were subsequently captured and documented using a Gel DocTM EZ system equipped with Image LabTM imaging and analysis software (Bio-Rad Laboratories, USA). ..

    Imaging:

    Article Title: Isothermal and protein-free cascade catalytic hairpin assembly induced-DNAzyme sensing strategy for sensitive miRNA analysis
    Article Snippet: Electrophoresis was performed using a gel electrophoresis unit (Bio-Rad Laboratories, USA) submerged in 1× TBE running buffer (89 mM Tris-borate, 2 mM EDTA, pH 8.3). .. Separation was carried out at a constant voltage of 80 V for 70 min. Post-electrophoresis, the gel was immersed in a diluted solution of Super GelRedTM nucleic acid stain for 20 min. Gel images were subsequently captured and documented using a Gel DocTM EZ system equipped with Image LabTM imaging and analysis software (Bio-Rad Laboratories, USA). ..

    Article Title: Isothermal and protein-free cascade catalytic hairpin assembly induced-DNAzyme sensing strategy for sensitive miRNA analysis.
    Article Snippet: Electrophoresis was performed using a gel electrophoresis unit (Bio-Rad Laboratories, USA) submerged in 1× TBE running buffer (89 mM Tris-borate, 2 mM EDTA, pH 8.3). .. Separation was carried out at a constant voltage of 80 V for 70 min. Post-electrophoresis, the gel was immersed in a diluted solution of Super GelRedTM nucleic acid stain for 20 min. Gel images were subsequently captured and documented using a Gel DocTM EZ system equipped with Image LabTM imaging and analysis software (Bio-Rad Laboratories, USA). ..

    Software:

    Article Title: Isothermal and protein-free cascade catalytic hairpin assembly induced-DNAzyme sensing strategy for sensitive miRNA analysis
    Article Snippet: Electrophoresis was performed using a gel electrophoresis unit (Bio-Rad Laboratories, USA) submerged in 1× TBE running buffer (89 mM Tris-borate, 2 mM EDTA, pH 8.3). .. Separation was carried out at a constant voltage of 80 V for 70 min. Post-electrophoresis, the gel was immersed in a diluted solution of Super GelRedTM nucleic acid stain for 20 min. Gel images were subsequently captured and documented using a Gel DocTM EZ system equipped with Image LabTM imaging and analysis software (Bio-Rad Laboratories, USA). ..

    Article Title: Shen-Ling-Bai-Zhu-San alleviates ulcerative colitis by enhancing mitophagy via the Nrf2/PINK1/Parkin pathway.
    Article Snippet: weight loss, diarrhea, rectal bleeding, abdominal pain, and mucosal inflammation that spreads from the rectum to the distal colon(Chen et al. 2023).. Currently, 5-aminosalicylic acid drugs, corticosteroids, immunosuppressants, and biologics represent the most prevalent non-surgical treatment options for UC, but the one-year clinical remission rate hovers at merely around 40% (Liang et al. 2024).. Surgical intervention presents itself as the ultimate remedy for eradicating UC, but postoperative complications like stenosis and anastomotic fistula significantly undermine the patients’ quality of life (Kobayashi et al. 2020).

    Article Title: Isothermal and protein-free cascade catalytic hairpin assembly induced-DNAzyme sensing strategy for sensitive miRNA analysis.
    Article Snippet: Electrophoresis was performed using a gel electrophoresis unit (Bio-Rad Laboratories, USA) submerged in 1× TBE running buffer (89 mM Tris-borate, 2 mM EDTA, pH 8.3). .. Separation was carried out at a constant voltage of 80 V for 70 min. Post-electrophoresis, the gel was immersed in a diluted solution of Super GelRedTM nucleic acid stain for 20 min. Gel images were subsequently captured and documented using a Gel DocTM EZ system equipped with Image LabTM imaging and analysis software (Bio-Rad Laboratories, USA). ..

    Article Title: Surface Acoustic Waves-Based Molecular Recognition of a Collagen Receptor on Human Erythrocytes.
    Article Snippet: The membranes were incubated for 45 min with horseradish peroxidase (HRP) linked secondary antibody diluted in blocking buffer (Table 3) after 5 washes with deionized water and 5 min incubation with TBS-T. Then the membranes were washed 7 times with deionized water and incubated for 5 min in TBS-T. At the end, the chemiluminescent HRP substrate (Millipore, Burlington, MA, USA) was applied to the blots for 5 min, initiating the chemiluminescence reaction catalyzed by the peroxidase conjugated to the secondary antibody. .. The emitted light was detected with a ChemiDoc XRS system (Bio-Rad, Hercules, CA, USA); the image acquisition was conducted using Quantity One 1-D Analysis software v4.6.9 (Bio-Rad, Hercules, CA, USA). .. FIJI-ImageJ 2.0.0-rc-2 software was used for image processing analysis [68].

    Variant Assay:

    Article Title: Harnessing liquid biopsy to unveil RAS-MEK pathway somatic pathogenic variants in extracranial arterio-venous malformations.
    Article Snippet: .. Orthogonal confirmation ddPCR –NM_004985(KRAS):c.35 G > A (p.G12D) [KRAS p.G12D]was analysed using PrimePCR variant detection assay dHsaMDV2510596 (KRAS:c.35 G > A, p.G12D, 6-FAM, KRAS WT reference gene, HEX; Bio-Rad Laboratories) as described in Kahana-Edwin et al., 202119. .. Controls included a non-template control (NTC), which contained purified water instead of cfDNA, and the artificial cfDNA reference standards described above (Horizon Discovery).

    Article Title: Harnessing liquid biopsy to unveil RAS-MEK pathway somatic pathogenic variants in extracranial arterio-venous malformations
    Article Snippet: .. ddPCR – NM_004985 (KRAS):c.35 G > A (p.G12D) [KRAS p.G12D] was analysed using PrimePCR variant detection assay dHsaMDV2510596 (KRAS:c.35 G > A, p.G12D, 6-FAM, KRAS WT reference gene, HEX; Bio-Rad Laboratories) as described in Kahana-Edwin et al., 2021 . .. Controls included a non-template control (NTC), which contained purified water instead of cfDNA, and the artificial cfDNA reference standards described above (Horizon Discovery).

    Detection Assay:

    Article Title: Harnessing liquid biopsy to unveil RAS-MEK pathway somatic pathogenic variants in extracranial arterio-venous malformations.
    Article Snippet: .. Orthogonal confirmation ddPCR –NM_004985(KRAS):c.35 G > A (p.G12D) [KRAS p.G12D]was analysed using PrimePCR variant detection assay dHsaMDV2510596 (KRAS:c.35 G > A, p.G12D, 6-FAM, KRAS WT reference gene, HEX; Bio-Rad Laboratories) as described in Kahana-Edwin et al., 202119. .. Controls included a non-template control (NTC), which contained purified water instead of cfDNA, and the artificial cfDNA reference standards described above (Horizon Discovery).

    Article Title: Harnessing liquid biopsy to unveil RAS-MEK pathway somatic pathogenic variants in extracranial arterio-venous malformations
    Article Snippet: .. ddPCR – NM_004985 (KRAS):c.35 G > A (p.G12D) [KRAS p.G12D] was analysed using PrimePCR variant detection assay dHsaMDV2510596 (KRAS:c.35 G > A, p.G12D, 6-FAM, KRAS WT reference gene, HEX; Bio-Rad Laboratories) as described in Kahana-Edwin et al., 2021 . .. Controls included a non-template control (NTC), which contained purified water instead of cfDNA, and the artificial cfDNA reference standards described above (Horizon Discovery).

    Quantitative RT-PCR:

    Article Title: Exploring the differentiation potential of adipose tissue-derived mesenchymal stromal/stem cells and progenitor buccal epithelial cells into urothelial cells
    Article Snippet: .. RT-qPCR was performed using PrimePCRTM primers ( , Bio-Rad, Hercules, CA, United States) and the LightCycler 480 SYBR Green I Master Kit (Roche Diagnostics, Basel, Switzerland). ..

    SYBR Green Assay:

    Article Title: Exploring the differentiation potential of adipose tissue-derived mesenchymal stromal/stem cells and progenitor buccal epithelial cells into urothelial cells
    Article Snippet: .. RT-qPCR was performed using PrimePCRTM primers ( , Bio-Rad, Hercules, CA, United States) and the LightCycler 480 SYBR Green I Master Kit (Roche Diagnostics, Basel, Switzerland). ..



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    Image Search Results


    Open Field test in different experimental groups (control, sham, and α-syn) at one, two, and four months post-injection. Spontaneous global activity (a) , locomotion (b) , and mean velocity (c) were measured in an Open Field arena. Activity detection was fully automated using custom-designed software Actitrack (Panlab, Spain). Data are presented as mean ± SEM. * p < 0.05, ** p < 0.01 (one-way ANOVA with post hoc corrections; n = 12 in each experimental group). (d) Temporal analysis assessing the progression of global activity. Data are presented as mean ± SEM. ***(time) p < 0.001; # (α-syn vs. control) p < 0.05 (multivariate linear regression analysis)

    Journal: Brain Structure & Function

    Article Title: Temporal progression of pathological features in an α-synuclein overexpression model of Parkinson’s disease

    doi: 10.1007/s00429-025-02959-9

    Figure Lengend Snippet: Open Field test in different experimental groups (control, sham, and α-syn) at one, two, and four months post-injection. Spontaneous global activity (a) , locomotion (b) , and mean velocity (c) were measured in an Open Field arena. Activity detection was fully automated using custom-designed software Actitrack (Panlab, Spain). Data are presented as mean ± SEM. * p < 0.05, ** p < 0.01 (one-way ANOVA with post hoc corrections; n = 12 in each experimental group). (d) Temporal analysis assessing the progression of global activity. Data are presented as mean ± SEM. ***(time) p < 0.001; # (α-syn vs. control) p < 0.05 (multivariate linear regression analysis)

    Article Snippet: The detection of global activity, locomotion and mean velocity was fully automated using the custom-designed software Actitrack (Panlab, Spain).

    Techniques: Control, Injection, Activity Assay, Software