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imagequant image analysis software  (Cytiva Europe)


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    Structured Review

    Cytiva Europe imagequant image analysis software
    Imagequant Image Analysis Software, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/image+analysis+software+imagequant/pmc11344278-232-21-25
    Average 86 stars, based on 1 article reviews
    imagequant image analysis software - by Bioz Stars, 2026-10
    86/100 stars

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    Related Articles

    Fluorescence:

    Article Title: Polymerase incorporation of fluorescein or rhodamine modified 2'-deoxyuridine-5'-triphosphates into double-stranded DNA for direct electrochemical detection.
    Article Snippet: The 2′-deoxyuridine-5′-triphosphates modified with fluorescein (dUTP-Fl) or rhodamine (dUTP-Rh) were tested as bearers of electroactive labels and as proper substrates for polymerases used in polymerase chain reaction (PCR) and isothermal recombinase polymerase amplification (RPA) with the aim of electrochemical detection of double-stranded DNA (dsDNA) amplification products.. For this purpose, electrochemical behavior of free fluorescein and rhodamine as well as the modified nucleotides, dUTP-Fl and dUTP-Rh, was studied by cyclic (CV) and square wave (SWV) voltammetry on carbon screen printed electrodes.. Both free fluorescein and dUTP-Fl underwent a two-step oxidation at the peak potentials (Ep) of 0.6–0.7 V and 0.8–0.9 V (phosphate buffer, pH 7.4).

    Modification:

    Article Title: Polymerase incorporation of fluorescein or rhodamine modified 2'-deoxyuridine-5'-triphosphates into double-stranded DNA for direct electrochemical detection.
    Article Snippet: The 2′-deoxyuridine-5′-triphosphates modified with fluorescein (dUTP-Fl) or rhodamine (dUTP-Rh) were tested as bearers of electroactive labels and as proper substrates for polymerases used in polymerase chain reaction (PCR) and isothermal recombinase polymerase amplification (RPA) with the aim of electrochemical detection of double-stranded DNA (dsDNA) amplification products.. For this purpose, electrochemical behavior of free fluorescein and rhodamine as well as the modified nucleotides, dUTP-Fl and dUTP-Rh, was studied by cyclic (CV) and square wave (SWV) voltammetry on carbon screen printed electrodes.. Both free fluorescein and dUTP-Fl underwent a two-step oxidation at the peak potentials (Ep) of 0.6–0.7 V and 0.8–0.9 V (phosphate buffer, pH 7.4).

    Software:

    Article Title: Polymerase incorporation of fluorescein or rhodamine modified 2'-deoxyuridine-5'-triphosphates into double-stranded DNA for direct electrochemical detection.
    Article Snippet: The 2′-deoxyuridine-5′-triphosphates modified with fluorescein (dUTP-Fl) or rhodamine (dUTP-Rh) were tested as bearers of electroactive labels and as proper substrates for polymerases used in polymerase chain reaction (PCR) and isothermal recombinase polymerase amplification (RPA) with the aim of electrochemical detection of double-stranded DNA (dsDNA) amplification products.. For this purpose, electrochemical behavior of free fluorescein and rhodamine as well as the modified nucleotides, dUTP-Fl and dUTP-Rh, was studied by cyclic (CV) and square wave (SWV) voltammetry on carbon screen printed electrodes.. Both free fluorescein and dUTP-Fl underwent a two-step oxidation at the peak potentials (Ep) of 0.6–0.7 V and 0.8–0.9 V (phosphate buffer, pH 7.4).

    Article Title: Bacterial hyaluronidase and process for its production
    Article Snippet: The molecular weight of the purified protein was assessed by comparison with standard low molecular weight proteins (BIO-RAD). .. The polyacrylamide gels suitably stained with Silver Stain Plus (BIO_RAD) or Coomassie (BIO-RAD) after the electrophoretic run, were acquired by a laboratory image capturing device ImageQuant 300 TL (GE Healthcare), while (quantitative and qualitative) assays were performed using the image analysis software ImageQuant TL (GE Healthcare). .. The N-terminal amino acid sequencing was carried out according to Edman's degradation method using an automated protein sequencer in pulsed liquid phase (ABI-Perkin Elmer Mod.

    Article Title: TGF-receptor II isoform, fusion peptide, methods of treatment and methods in vitro
    Article Snippet: .. For densitometry analysis of the arrays, Typhoon 9410 Variable mode Imager (GE Healthcare Life Sciences) was used, and signal intensity values were measured using the Image analysis software ImageQuant TL 7.0 (GE Healthcare Life Sciences). .. Microarray data were analyzed with RayBio® Antibody Array Analysis Tool.

    Staining:

    Article Title: Bacterial hyaluronidase and process for its production
    Article Snippet: The molecular weight of the purified protein was assessed by comparison with standard low molecular weight proteins (BIO-RAD). .. The polyacrylamide gels suitably stained with Silver Stain Plus (BIO_RAD) or Coomassie (BIO-RAD) after the electrophoretic run, were acquired by a laboratory image capturing device ImageQuant 300 TL (GE Healthcare), while (quantitative and qualitative) assays were performed using the image analysis software ImageQuant TL (GE Healthcare). .. The N-terminal amino acid sequencing was carried out according to Edman's degradation method using an automated protein sequencer in pulsed liquid phase (ABI-Perkin Elmer Mod.

    Silver Staining:

    Article Title: Bacterial hyaluronidase and process for its production
    Article Snippet: The molecular weight of the purified protein was assessed by comparison with standard low molecular weight proteins (BIO-RAD). .. The polyacrylamide gels suitably stained with Silver Stain Plus (BIO_RAD) or Coomassie (BIO-RAD) after the electrophoretic run, were acquired by a laboratory image capturing device ImageQuant 300 TL (GE Healthcare), while (quantitative and qualitative) assays were performed using the image analysis software ImageQuant TL (GE Healthcare). .. The N-terminal amino acid sequencing was carried out according to Edman's degradation method using an automated protein sequencer in pulsed liquid phase (ABI-Perkin Elmer Mod.



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