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bio rad cfx connect real time pcr detection system  (Bio-Rad)


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    Bio-Rad bio rad cfx connect real time pcr detection system
    PCNA AI-CADD molecule thermal shift assay screening hits . AI-CADD screening: Left , plot of normalized melt curves of compounds + PCNA melt. Center , normalized derivative RFU of melt curve data. The DMSO control is plotted in black dashed lines. Right , . Calculated Δ Tm values of 19 AI-CADD hits. Thermal shift assays were performed using a Bio-Rad <t>CFX</t> <t>Connect</t> <t>Real-Time</t> <t>PCR</t> Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM. The reaction plates were heated from 25 °C to 95 °C with heating increments of 0.5 °C/min. Fluorescence intensity was measured within the excitation/emission ranges 470–505/540–700 nm. A negative control of 100% DMSO was included in each assay to obtain an apo- PCNA melting temperature (Tm apo ). The melting temperature of each reaction well was extrapolated from the midpoint of excitation of the produced melt curves by the CFX Maestro Software (Bio-Rad). The thermal shift values were calculated using the following equation: ΔTm = Tm + compound – Tm apo .
    Bio Rad Cfx Connect Real Time Pcr Detection System, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 98/100, based on 4019 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cfx+connect+real+time+pcr+detection+system+bio+rad/CFX+Maestro+Software/pmc12930076-116-7-7
    Average 98 stars, based on 4019 article reviews
    bio rad cfx connect real time pcr detection system - by Bioz Stars, 2026-10
    98/100 stars

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    1) Product Images from "Screening for novel chemical scaffolds targeting PCNA identifies the Hsp90alpha inhibitor SNX-2112"

    Article Title: Screening for novel chemical scaffolds targeting PCNA identifies the Hsp90alpha inhibitor SNX-2112

    Journal: Current Research in Structural Biology

    doi: 10.1016/j.crstbi.2026.100183

    PCNA AI-CADD molecule thermal shift assay screening hits . AI-CADD screening: Left , plot of normalized melt curves of compounds + PCNA melt. Center , normalized derivative RFU of melt curve data. The DMSO control is plotted in black dashed lines. Right , . Calculated Δ Tm values of 19 AI-CADD hits. Thermal shift assays were performed using a Bio-Rad CFX Connect Real-Time PCR Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM. The reaction plates were heated from 25 °C to 95 °C with heating increments of 0.5 °C/min. Fluorescence intensity was measured within the excitation/emission ranges 470–505/540–700 nm. A negative control of 100% DMSO was included in each assay to obtain an apo- PCNA melting temperature (Tm apo ). The melting temperature of each reaction well was extrapolated from the midpoint of excitation of the produced melt curves by the CFX Maestro Software (Bio-Rad). The thermal shift values were calculated using the following equation: ΔTm = Tm + compound – Tm apo .
    Figure Legend Snippet: PCNA AI-CADD molecule thermal shift assay screening hits . AI-CADD screening: Left , plot of normalized melt curves of compounds + PCNA melt. Center , normalized derivative RFU of melt curve data. The DMSO control is plotted in black dashed lines. Right , . Calculated Δ Tm values of 19 AI-CADD hits. Thermal shift assays were performed using a Bio-Rad CFX Connect Real-Time PCR Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM. The reaction plates were heated from 25 °C to 95 °C with heating increments of 0.5 °C/min. Fluorescence intensity was measured within the excitation/emission ranges 470–505/540–700 nm. A negative control of 100% DMSO was included in each assay to obtain an apo- PCNA melting temperature (Tm apo ). The melting temperature of each reaction well was extrapolated from the midpoint of excitation of the produced melt curves by the CFX Maestro Software (Bio-Rad). The thermal shift values were calculated using the following equation: ΔTm = Tm + compound – Tm apo .

    Techniques Used: Thermal Shift Assay, Control, Real-time Polymerase Chain Reaction, Concentration Assay, Recombinant, Purification, Fluorescence, Negative Control, Produced, Maestro Software

    Related Articles

    Real-time Polymerase Chain Reaction:

    Article Title: Effect of Nutraceutical Supplementation and Mediterranean Hypocaloric Diet on Calculated Steatosis Indices and Inflammation: Clinical and In Vitro Evidences
    Article Snippet: .. The qPCR was performed using iTaq Universal SYBR Green Supermix (Bio‐Rad) on a CFX Connect Real‐Time PCR Detection System (Bio‐Rad) with the following cycling conditions: 95°C for 3 min, then 40 cycles of 95°C for 15 s, and 60°C for 30 s, followed by melting curve analysis. ..

    Article Title: Ex Vivo Spatiotemporal Characterization of Spermatogenesis in Mouse Testicular Organoids
    Article Snippet: For gene expression analysis, mRNA was first reverse‐transcribed into cDNA using the PrimeScript RT Master Mix (TAKARA). .. Subsequently, quantitative PCR (qPCR) was performed with ChamQ SYBR qPCR Master Mix (Vazyme Biotech) on a CFX Connect Real‐Time PCR Detection System (Bio‐Rad) following the manufacturer's instructions. ..

    Article Title: DNA Aptamers Targeting BcSOD1: A Novel Strategy for Controlling Botrytis cinerea in Sustainable Agriculture
    Article Snippet: .. The assay was carried out in a CFX Connect Real‐Time PCR detection system (Bio‐Rad) with SsoFast EvaGreen Supermix (Bio‐Rad). ..

    Article Title: Gold Nanoturf‐Mediated Wireless Photothermal Upregulation of Human Adipose‐Derived Stem Cell Spheroids for Synergistic Skin‐Wound Closure
    Article Snippet: .. The SsoAdvanceed Universal SYBR Green Supermix kit (Bio‐Rad, Hercules, CA, USA) and CFX Connect real‐time PCR detection system (Bio‐Rad) were used for qRT‐PCR. ..

    Article Title: Macropinocytic Uptake and pH‐Responsive Endolysosomal Processing Drive Sustained Chemotherapeutic Efficacy of High‐Load Core@Shell Nanocarriers in Colorectal Cancer
    Article Snippet: Reverse transcription was performed using SuperScript (Invitrogen) with 1 μg of total RNA, following the supplier's instructions. .. The resulting cDNA was used as a template for quantitative real‐time PCR, conducted in triplicate on a CFX Connect Real‐Time PCR Detection System (Bio‐Rad) in a 25 μl reaction volume. .. Gene expression levels were quantified using SYBR Green I (Invitrogen), and relative transcript levels were calculated using the 2 ‐ΔΔCt method after normalization to the housekeeping gene RPLP0.

    Article Title: Identification of Genes Involved in Resistance to Flavescence Dorée Disease of Grapevine: A Model Study Using Arabidopsis thaliana
    Article Snippet: .. The presence of CYp and FDp was verified by quantitative PCR (qPCR) in a CFX Connect Real‐Time PCR Detection System (Bio‐Rad), according to Galetto et al. ( ) and Pelletier et al. , respectively. .. Universal phytoplasma primers CYS2Fw/Rv and FAM‐labelled TaqMan CYS2Probe designed on ribosomal 16S rRNA gene sequence (Marzachí and Bosco ) were used to detect CYp.

    Article Title: Silencing of the Metabolic Gene HKDC1 Is Associated With Aging and Neurodegeneration in Mice and Humans
    Article Snippet: .. Data were collected and analyzed using the CFX Connect Real‐Time PCR Detection System (Bio‐Rad) and CFX Maestro 2.2 software (Bio‐Rad), respectively. ..

    Article Title: Colistin and Biofilm‐Related Genes of Positive Escherichia coli O157:H7 in Cattle ( Bos taurus ) Carcasses Antibiotic Resistance Profiles, Biofilm and Molecular Characterisation of Isolates
    Article Snippet: .. CFX Connect Real‐Time PCR Detection System (Bio‐Rad) was used for expression analysis. qRT‐PCR analysis was performed using SYBR green (Biorad) with 10 pmol of each primer and 5 μL of cDNA in a 20 μL reaction volume in duplicate. ..

    SYBR Green Assay:

    Article Title: Effect of Nutraceutical Supplementation and Mediterranean Hypocaloric Diet on Calculated Steatosis Indices and Inflammation: Clinical and In Vitro Evidences
    Article Snippet: .. The qPCR was performed using iTaq Universal SYBR Green Supermix (Bio‐Rad) on a CFX Connect Real‐Time PCR Detection System (Bio‐Rad) with the following cycling conditions: 95°C for 3 min, then 40 cycles of 95°C for 15 s, and 60°C for 30 s, followed by melting curve analysis. ..

    Article Title: Gold Nanoturf‐Mediated Wireless Photothermal Upregulation of Human Adipose‐Derived Stem Cell Spheroids for Synergistic Skin‐Wound Closure
    Article Snippet: .. The SsoAdvanceed Universal SYBR Green Supermix kit (Bio‐Rad, Hercules, CA, USA) and CFX Connect real‐time PCR detection system (Bio‐Rad) were used for qRT‐PCR. ..

    Article Title: Colistin and Biofilm‐Related Genes of Positive Escherichia coli O157:H7 in Cattle ( Bos taurus ) Carcasses Antibiotic Resistance Profiles, Biofilm and Molecular Characterisation of Isolates
    Article Snippet: .. CFX Connect Real‐Time PCR Detection System (Bio‐Rad) was used for expression analysis. qRT‐PCR analysis was performed using SYBR green (Biorad) with 10 pmol of each primer and 5 μL of cDNA in a 20 μL reaction volume in duplicate. ..

    Software:

    Article Title: Silencing of the Metabolic Gene HKDC1 Is Associated With Aging and Neurodegeneration in Mice and Humans
    Article Snippet: .. Data were collected and analyzed using the CFX Connect Real‐Time PCR Detection System (Bio‐Rad) and CFX Maestro 2.2 software (Bio‐Rad), respectively. ..

    Expressing:

    Article Title: Colistin and Biofilm‐Related Genes of Positive Escherichia coli O157:H7 in Cattle ( Bos taurus ) Carcasses Antibiotic Resistance Profiles, Biofilm and Molecular Characterisation of Isolates
    Article Snippet: .. CFX Connect Real‐Time PCR Detection System (Bio‐Rad) was used for expression analysis. qRT‐PCR analysis was performed using SYBR green (Biorad) with 10 pmol of each primer and 5 μL of cDNA in a 20 μL reaction volume in duplicate. ..



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    PCNA AI-CADD molecule thermal shift assay screening hits . AI-CADD screening: Left , plot of normalized melt curves of compounds + PCNA melt. Center , normalized derivative RFU of melt curve data. The DMSO control is plotted in black dashed lines. Right , . Calculated Δ Tm values of 19 AI-CADD hits. Thermal shift assays were performed using a Bio-Rad <t>CFX</t> <t>Connect</t> <t>Real-Time</t> <t>PCR</t> Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM. The reaction plates were heated from 25 °C to 95 °C with heating increments of 0.5 °C/min. Fluorescence intensity was measured within the excitation/emission ranges 470–505/540–700 nm. A negative control of 100% DMSO was included in each assay to obtain an apo- PCNA melting temperature (Tm apo ). The melting temperature of each reaction well was extrapolated from the midpoint of excitation of the produced melt curves by the CFX Maestro Software (Bio-Rad). The thermal shift values were calculated using the following equation: ΔTm = Tm + compound – Tm apo .
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    PCNA AI-CADD molecule thermal shift assay screening hits . AI-CADD screening: Left , plot of normalized melt curves of compounds + PCNA melt. Center , normalized derivative RFU of melt curve data. The DMSO control is plotted in black dashed lines. Right , . Calculated Δ Tm values of 19 AI-CADD hits. Thermal shift assays were performed using a Bio-Rad <t>CFX</t> <t>Connect</t> <t>Real-Time</t> <t>PCR</t> Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM. The reaction plates were heated from 25 °C to 95 °C with heating increments of 0.5 °C/min. Fluorescence intensity was measured within the excitation/emission ranges 470–505/540–700 nm. A negative control of 100% DMSO was included in each assay to obtain an apo- PCNA melting temperature (Tm apo ). The melting temperature of each reaction well was extrapolated from the midpoint of excitation of the produced melt curves by the CFX Maestro Software (Bio-Rad). The thermal shift values were calculated using the following equation: ΔTm = Tm + compound – Tm apo .
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    PCNA AI-CADD molecule thermal shift assay screening hits . AI-CADD screening: Left , plot of normalized melt curves of compounds + PCNA melt. Center , normalized derivative RFU of melt curve data. The DMSO control is plotted in black dashed lines. Right , . Calculated Δ Tm values of 19 AI-CADD hits. Thermal shift assays were performed using a Bio-Rad <t>CFX</t> <t>Connect</t> <t>Real-Time</t> <t>PCR</t> Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM. The reaction plates were heated from 25 °C to 95 °C with heating increments of 0.5 °C/min. Fluorescence intensity was measured within the excitation/emission ranges 470–505/540–700 nm. A negative control of 100% DMSO was included in each assay to obtain an apo- PCNA melting temperature (Tm apo ). The melting temperature of each reaction well was extrapolated from the midpoint of excitation of the produced melt curves by the CFX Maestro Software (Bio-Rad). The thermal shift values were calculated using the following equation: ΔTm = Tm + compound – Tm apo .
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    PCNA AI-CADD molecule thermal shift assay screening hits . AI-CADD screening: Left , plot of normalized melt curves of compounds + PCNA melt. Center , normalized derivative RFU of melt curve data. The DMSO control is plotted in black dashed lines. Right , . Calculated Δ Tm values of 19 AI-CADD hits. Thermal shift assays were performed using a Bio-Rad <t>CFX</t> <t>Connect</t> <t>Real-Time</t> <t>PCR</t> Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM. The reaction plates were heated from 25 °C to 95 °C with heating increments of 0.5 °C/min. Fluorescence intensity was measured within the excitation/emission ranges 470–505/540–700 nm. A negative control of 100% DMSO was included in each assay to obtain an apo- PCNA melting temperature (Tm apo ). The melting temperature of each reaction well was extrapolated from the midpoint of excitation of the produced melt curves by the CFX Maestro Software (Bio-Rad). The thermal shift values were calculated using the following equation: ΔTm = Tm + compound – Tm apo .
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    PCNA AI-CADD molecule thermal shift assay screening hits . AI-CADD screening: Left , plot of normalized melt curves of compounds + PCNA melt. Center , normalized derivative RFU of melt curve data. The DMSO control is plotted in black dashed lines. Right , . Calculated Δ Tm values of 19 AI-CADD hits. Thermal shift assays were performed using a Bio-Rad CFX Connect Real-Time PCR Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM. The reaction plates were heated from 25 °C to 95 °C with heating increments of 0.5 °C/min. Fluorescence intensity was measured within the excitation/emission ranges 470–505/540–700 nm. A negative control of 100% DMSO was included in each assay to obtain an apo- PCNA melting temperature (Tm apo ). The melting temperature of each reaction well was extrapolated from the midpoint of excitation of the produced melt curves by the CFX Maestro Software (Bio-Rad). The thermal shift values were calculated using the following equation: ΔTm = Tm + compound – Tm apo .

    Journal: Current Research in Structural Biology

    Article Title: Screening for novel chemical scaffolds targeting PCNA identifies the Hsp90alpha inhibitor SNX-2112

    doi: 10.1016/j.crstbi.2026.100183

    Figure Lengend Snippet: PCNA AI-CADD molecule thermal shift assay screening hits . AI-CADD screening: Left , plot of normalized melt curves of compounds + PCNA melt. Center , normalized derivative RFU of melt curve data. The DMSO control is plotted in black dashed lines. Right , . Calculated Δ Tm values of 19 AI-CADD hits. Thermal shift assays were performed using a Bio-Rad CFX Connect Real-Time PCR Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM. The reaction plates were heated from 25 °C to 95 °C with heating increments of 0.5 °C/min. Fluorescence intensity was measured within the excitation/emission ranges 470–505/540–700 nm. A negative control of 100% DMSO was included in each assay to obtain an apo- PCNA melting temperature (Tm apo ). The melting temperature of each reaction well was extrapolated from the midpoint of excitation of the produced melt curves by the CFX Maestro Software (Bio-Rad). The thermal shift values were calculated using the following equation: ΔTm = Tm + compound – Tm apo .

    Article Snippet: Thermal shift assays were performed using a Bio-Rad CFX Connect Real-Time PCR Detection System. and the final concentration of recombinant purified PCNA was 9 μM, and the final concentration of each compound was 1 mM.

    Techniques: Thermal Shift Assay, Control, Real-time Polymerase Chain Reaction, Concentration Assay, Recombinant, Purification, Fluorescence, Negative Control, Produced, Maestro Software