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deconvolution software mass hunter unknown analysis 7.0  (Agilent technologies)


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    Agilent technologies deconvolution software mass hunter unknown analysis 7.0
    Deconvolution Software Mass Hunter Unknown Analysis 7.0, supplied by Agilent technologies, 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/deconvolution+software+analysis/pm37511506-256-3-5
    Average 90 stars, based on 1 article reviews
    deconvolution software mass hunter unknown analysis 7.0 - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Software:

    Article Title: Acetylene containing cyclo(L-Tyr-L-Tyr)-analogs as mechanism-based inhibitors of CYP121A1 from Mycobacterium tuberculosis.
    Article Snippet: .. The protein masses were calculated by deconvolution of the m/z-clusters obtained using Agilent MassHunter Qualitative 13 analysis software (version B.05.00). ..

    Article Title: NanoLC-EI-MS: Perspectives in Biochemical Analysis.
    Article Snippet: .. However, by employing deconvolution software (Agilent Mass Hunter Unknown Analysis 7.0), a distinct signal emerged beneath a prominent matrix peak, conclusively identified as benzo[a]pyrene (Figure 3). ..

    Article Title: The omnivorous predator Macrolophus pygmaeus induces production of plant volatiles that attract a specialist predator
    Article Snippet: It has become clear that omnivorous predators can induce plant defences that affect the performance and host plant choice of herbivores.. They are also known to induce the production of plant volatiles that can affect the behaviour of herbivores searching for plants.. These volatiles may also affect the searching behaviour of other predators, which was investigated here.

    Article Title: Volatile Metabolome and Aroma Differences of Six Cultivars of Prunus mume Blossoms
    Article Snippet: The total ion chromatograms (TIC) obtained in GC-MS analysis were checked using Agilent MassHunter Qualitative Analysis software (B.07.00, Agilent Technologies Inc., Palo Alto, CA, USA). .. Deconvolution processing, peak picking, and mass spectrometry comparison were performed by Agilent MassHunter Unknowns Analysis software (B.07.01, Agilent Technologies Inc., Palo Alto, CA, USA) and NIST 11 library (match factor > 75). ..

    Article Title: Control of Antibody Impurities Induced by Riboflavin in Culture Media During Production.
    Article Snippet: .. Mass determinations were performed on MassHunter Analysis deconvolution software (Agilent Technologies). ..

    other:

    Article Title: Discovery of Novel Benzothiazepinones as Irreversible Covalent Glycogen Synthase Kinase 3β Inhibitors for the Treatment of Acute Promyelocytic Leukemia.
    Article Snippet: Recently, irreversible inhibitors have attracted great interest in antitumors due to their advantages of forming covalent bonds to target proteins.. Herein, some benzothiazepinone compounds (BTZs) have been designed and synthesized as novel covalent GSK-3β inhibitors with high selectivity for the kinase panel.. The irreversible covalent binding mode was identified by kinetics and mass spectrometry, and the main labeled residue was confirmed to be the unique Cys14 that exists only in GSK-3β.

    Article Title: Mechanistic insights into the enzymatic activity of E3 ligase HOIL-1L and its regulation by the linear ubiquitin chain binding.
    Article Snippet: Mass deconvolution was later performed using Agilent MassHunter Qualitative Analysis B.06.00 software.

    Mass Spectrometry:

    Article Title: Volatile Metabolome and Aroma Differences of Six Cultivars of Prunus mume Blossoms
    Article Snippet: The total ion chromatograms (TIC) obtained in GC-MS analysis were checked using Agilent MassHunter Qualitative Analysis software (B.07.00, Agilent Technologies Inc., Palo Alto, CA, USA). .. Deconvolution processing, peak picking, and mass spectrometry comparison were performed by Agilent MassHunter Unknowns Analysis software (B.07.01, Agilent Technologies Inc., Palo Alto, CA, USA) and NIST 11 library (match factor > 75). ..

    Comparison:

    Article Title: Volatile Metabolome and Aroma Differences of Six Cultivars of Prunus mume Blossoms
    Article Snippet: The total ion chromatograms (TIC) obtained in GC-MS analysis were checked using Agilent MassHunter Qualitative Analysis software (B.07.00, Agilent Technologies Inc., Palo Alto, CA, USA). .. Deconvolution processing, peak picking, and mass spectrometry comparison were performed by Agilent MassHunter Unknowns Analysis software (B.07.01, Agilent Technologies Inc., Palo Alto, CA, USA) and NIST 11 library (match factor > 75). ..



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    Image Search Results


    Triple co-localization of β-catenin, NDRG1, and PKCα demonstrates the formation of a possible metabolon, decreasing β-catenin levels and nuclear localization. A – H , NDRG1 overexpression in PANC-1 cells significantly increases the co-localization between β-catenin, NDRG1, and PKCα. A and B , VC and NDRG1 overexpressing PANC-1 cells were incubated for 24 h/37 °C in the presence and absence of WNT3a (100 ng/ml). The cells were then examined for β-catenin ( green ), NDRG1 ( red ), and PKCα ( blue ) expression and triple co-localization ( white ) using confocal immunofluorescence microscopy. Studies were performed using a 100× objective at the same acquisition setting with Olympus Fluoview FV3000 software. Images were digitally magnified for better demonstration of the possible co-localization. The scale bar = 3 μm for all images except for the inset images, where the scale bar = 9 μm. C and D , deconvolution analysis was then implemented on the images in ( A and B ) using Olympus CellSens imaging software. White arrows demonstrate triple co-localization and possible formation of the metabolon. The scale bar = 3 μm for all deconvolution images except for the inset images, where the scale bar = 1.8 μm. In all studies, the images are representative of three experiments, and the quantitative analysis of the pixel intensities is shown for ( E ) β-catenin; ( F ) NDRG1; ( G ) PKCα; and ( H ) Co-localization between β-catenin, NDRG1, and PKCα. Quantitative analyses were performed using ImageJ software and were presented as the mean ± SD ( n = 3). Analysis of pixel intensity and co-localization were performed using 24 cells. Statistical significance is denoted as ∗∗ p < 0.01 and ∗∗∗ p < 0.001 comparing NDRG1 overexpressing PANC-1 cells in the presence and absence of WNT3a to VC cells in the absence of WNT3a; or ### p < 0.001 comparing NDRG1 overexpressing PANC-1 cells to VC cells in the presence of WNT3a.

    Journal: The Journal of Biological Chemistry

    Article Title: Multi-modal mechanisms of the metastasis suppressor, NDRG1: Inhibition of WNT/β-catenin signaling by stabilization of protein kinase Cα

    doi: 10.1016/j.jbc.2024.107417

    Figure Lengend Snippet: Triple co-localization of β-catenin, NDRG1, and PKCα demonstrates the formation of a possible metabolon, decreasing β-catenin levels and nuclear localization. A – H , NDRG1 overexpression in PANC-1 cells significantly increases the co-localization between β-catenin, NDRG1, and PKCα. A and B , VC and NDRG1 overexpressing PANC-1 cells were incubated for 24 h/37 °C in the presence and absence of WNT3a (100 ng/ml). The cells were then examined for β-catenin ( green ), NDRG1 ( red ), and PKCα ( blue ) expression and triple co-localization ( white ) using confocal immunofluorescence microscopy. Studies were performed using a 100× objective at the same acquisition setting with Olympus Fluoview FV3000 software. Images were digitally magnified for better demonstration of the possible co-localization. The scale bar = 3 μm for all images except for the inset images, where the scale bar = 9 μm. C and D , deconvolution analysis was then implemented on the images in ( A and B ) using Olympus CellSens imaging software. White arrows demonstrate triple co-localization and possible formation of the metabolon. The scale bar = 3 μm for all deconvolution images except for the inset images, where the scale bar = 1.8 μm. In all studies, the images are representative of three experiments, and the quantitative analysis of the pixel intensities is shown for ( E ) β-catenin; ( F ) NDRG1; ( G ) PKCα; and ( H ) Co-localization between β-catenin, NDRG1, and PKCα. Quantitative analyses were performed using ImageJ software and were presented as the mean ± SD ( n = 3). Analysis of pixel intensity and co-localization were performed using 24 cells. Statistical significance is denoted as ∗∗ p < 0.01 and ∗∗∗ p < 0.001 comparing NDRG1 overexpressing PANC-1 cells in the presence and absence of WNT3a to VC cells in the absence of WNT3a; or ### p < 0.001 comparing NDRG1 overexpressing PANC-1 cells to VC cells in the presence of WNT3a.

    Article Snippet: The images of visualized cells were then examined using Olympus Fluoview software, and in some studies, images were processed for deconvolution analysis with CellSens software (Olympus) to improve contrast and image resolution.

    Techniques: Over Expression, Incubation, Expressing, Immunofluorescence, Microscopy, Software, Imaging