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data analysis software origin (pro)  (OriginLab corp)


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    Structured Review

    OriginLab corp data analysis software origin (pro)
    Data Analysis Software Origin (Pro), supplied by OriginLab corp, 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/origin+analysis+software/data+analysis+software+origin/pmc08921600-103-11-18
    Average 90 stars, based on 1 article reviews
    data analysis software origin (pro) - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    other:

    Article Title: Multifunctional platform for future applications in cell and tissue engineering based on silicate phosphate hydroxyapatite co-doped with Li+, Eu3+ and Gd3+ ions
    Article Snippet: Although hydroxyapatite has established itself as a promising biomaterial for the simultaneous diagnosis and treatment of bone defects, several physicochemical properties can be further refined to achieve a specialized theranostic platform for cell and tissue engineering.. In this context, we synthesized silicate-substituted hydroxyapatites co-doped with Li, Eu3+, and Gd3+ ions (abbr.. as Si-HAp-LEG) using a microwave-assisted hydrothermal method.

    Article Title: Molecular bioprospection of Helianthus annuus L. (sunflower) cypselae for antidiabetic therapeutics through network pharmacology, density functional theory and molecular dynamics simulation
    Article Snippet: Helianthus annuus cypsela (sunflower) is a staple oilseed crop with significant therapeutic applications against diverse diseases including type 2 diabetes mellitus (T2DM).. Despite its reported antidiabetic potential, the implicated molecular mechanism of action is yet to be unravelled to date.. This study evaluated the molecular mechanism of the antidiabetic activity of sunflower cypsela using network pharmacology (NP), density functional theory, and molecular dynamics (MD) simulation approaches.

    Article Title: Salicylic Acid Solubility and Thermodynamic Dissociation Constant at Various Temperatures in Water: Variable Ionic Strength Titrimetric Analysis
    Article Snippet: Titrimetric methods were used to estimate the molar solubility and apparent acid dissociation constant (Kc) of salicylic acid in water.. This was done with varied ionic strength values ranging from 0.00 to 0.75 mol·L−1 and over a temperature range of 15 to 60 °C.. The thermodynamic dissociation constant (as pKa) of salicylic acid was found to be 2.985 at 25 °C.

    Software:

    Article Title: LIBS assisted PCA analysis of multiple rare-earth elements (La, Ce, Nd, Sm, and Yb) in phosphorite deposits
    Article Snippet: .. The data analysis software (Origin-pro/2022 (Origin Lab, USA)) was used for the PCA analysis. .. XLSTAT (version 2022 , addinsoft, USA) was used for the pre-processing of the data employed for the PCA.

    Article Title: Bioresorbable composites based on magnesium and hydroxyapatite for use in bone tissue engineering: focus on controlling and minimizing corrosion activity
    Article Snippet: A biodegradable matrix with a significant content of bioactive components can be applied for bone tissue replacement, including load-bearing applications in orthopedic surgery.. The study outlines the optimized procedure for the production of bioresorbable magnesium-hydroxyapatite (Mg-HA) composites and their corrosion resistance properties.. Composites were meticulously crafted by combining pure magnesium with microwavesynthesized hydroxyapatite nanopowder.

    Article Title: Durability of Ultem 9085 in Marine Environments: A Consideration in Fused Filament Fabrication of Structural Components
    Article Snippet: .. Baseline correction, normalization and smoothing of the Raman spectra were achieved by data analysis software (Origin, OriginLab, Northampton, MA, USA). ..

    Article Title: Robust Wet Milling Technique for Producing Micronized Ibuprofen Particles with Improved Solubility and Dissolution.
    Article Snippet: This study investigated a systematic approach for producing ibuprofen (IBF) particles with leucine by wet milling.. Using a high shear homogenizer, the particles size of the IBF was reduced.. Prepared IBF microparticles were freeze-dried and characterized by using Mastersizer, SEM, DSC, XRD, ATR-FTIR, and TGA.

    Article Title: Solid-State Nuclear Magnetic Resonance Investigations of the Lithium- and Sodium-Storage Mechanisms of Pyrolytic Phosphorus-Carbon Composites.
    Article Snippet: Raman spectroscopy mapping measurements were performed using a Renishaw InVia with a 2400 Lmm 1 grating and 512 nm laser. .. Peak fitting was performed using OriginLab Origin data analysis software using a Gaussian fit. .. Powder X-ray diffraction data were collected on a Malvern Panalytical X’Pert Pro instrument, equipped with an X’celerator detector using nonmonochromated CuKα radiation (λ= 1.5418 Å).



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    H3Q5ser stabilizes Taf3-PHD/H3K4me2 and Taf3-PHD/H3K4me3 complexes. ( A ) Experimental (blue) and fitted (red) spectra of free, ∼50% bound, and fully bound TAF3-PHD resonances E862 and C896 for H3K4me3/H3K4me3Q5ser complex. Transfer peaks indicated with *. Experimental spectrum of E862 is also shown separately for clarity. ( B ) <t>ITC</t> analysis of GST-tagged Taf3-PHD binding to H3K4me3 in yellow and H3K4me3Q5ser in navy blue. Top panel displays the raw heat change per injection of H3 peptide. Bottom panel represents the binding isotherm. The solid line represents the best fit to the one-set-of-sites model using MicroCal-ITC Origin 7 software.
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    H3Q5ser stabilizes Taf3-PHD/H3K4me2 and Taf3-PHD/H3K4me3 complexes. ( A ) Experimental (blue) and fitted (red) spectra of free, ∼50% bound, and fully bound TAF3-PHD resonances E862 and C896 for H3K4me3/H3K4me3Q5ser complex. Transfer peaks indicated with *. Experimental spectrum of E862 is also shown separately for clarity. ( B ) <t>ITC</t> analysis of GST-tagged Taf3-PHD binding to H3K4me3 in yellow and H3K4me3Q5ser in navy blue. Top panel displays the raw heat change per injection of H3 peptide. Bottom panel represents the binding isotherm. The solid line represents the best fit to the one-set-of-sites model using MicroCal-ITC Origin 7 software.
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    Image Search Results


    ITC traces of CP titrated with CBR126 wt (panel A) or CBR126 mut (panel B). Upper panels are raw traces of thermograms, with differential power for each injection of CBR. Lower panels are binding isotherms, with integrated enthalpy vs molar ratio. Fitted values for K D , with a stoichiometry of one, are listed.

    Journal: bioRxiv

    Article Title: Biochemical Functions of the Membrane-Binding Domain of CARMIL

    doi: 10.64898/2026.01.05.697744

    Figure Lengend Snippet: ITC traces of CP titrated with CBR126 wt (panel A) or CBR126 mut (panel B). Upper panels are raw traces of thermograms, with differential power for each injection of CBR. Lower panels are binding isotherms, with integrated enthalpy vs molar ratio. Fitted values for K D , with a stoichiometry of one, are listed.

    Article Snippet: Binding constants were determined by fitting the change in enthalpy to a single site binding model using MicroCal ITC Origin analysis software.

    Techniques: Injection, Binding Assay

    H3Q5ser stabilizes Taf3-PHD/H3K4me2 and Taf3-PHD/H3K4me3 complexes. ( A ) Experimental (blue) and fitted (red) spectra of free, ∼50% bound, and fully bound TAF3-PHD resonances E862 and C896 for H3K4me3/H3K4me3Q5ser complex. Transfer peaks indicated with *. Experimental spectrum of E862 is also shown separately for clarity. ( B ) ITC analysis of GST-tagged Taf3-PHD binding to H3K4me3 in yellow and H3K4me3Q5ser in navy blue. Top panel displays the raw heat change per injection of H3 peptide. Bottom panel represents the binding isotherm. The solid line represents the best fit to the one-set-of-sites model using MicroCal-ITC Origin 7 software.

    Journal: Nucleic Acids Research

    Article Title: Molecular determinants for recognition of serotonylated chromatin

    doi: 10.1093/nar/gkaf612

    Figure Lengend Snippet: H3Q5ser stabilizes Taf3-PHD/H3K4me2 and Taf3-PHD/H3K4me3 complexes. ( A ) Experimental (blue) and fitted (red) spectra of free, ∼50% bound, and fully bound TAF3-PHD resonances E862 and C896 for H3K4me3/H3K4me3Q5ser complex. Transfer peaks indicated with *. Experimental spectrum of E862 is also shown separately for clarity. ( B ) ITC analysis of GST-tagged Taf3-PHD binding to H3K4me3 in yellow and H3K4me3Q5ser in navy blue. Top panel displays the raw heat change per injection of H3 peptide. Bottom panel represents the binding isotherm. The solid line represents the best fit to the one-set-of-sites model using MicroCal-ITC Origin 7 software.

    Article Snippet: ITC data were subsequently analysed and fitted with the one-site binding model in the MicroCal ITC Origin Analysis software 7.0 (Table , Figs and , , and ).

    Techniques: Binding Assay, Injection, Software

    Taf3-PHD P881 and W894 form key interaction surface with the serotonin group. ( A ) ITC analysis of GST-tagged Taf3-PHD mutants, BPTF-PHD , PHF2-PHD, or PHF8-PHD with the peptides H3K4me3 (in yellow) and H3K4me3Q5ser (in blue). Top panels display the raw heat change per injection of H3 peptide. Bottom panels represent the binding isotherm. The solid line represents the best fit to the one-set-of-sites model using MicroCal-ITC Origin 7 software. ( B ) Multiple sequence alignment (MSA) of human PHD fingers for which high-resolution structures in complex with H3K4me3 are available (ASH1L PDB: 8VLF; BPTF(2) PDB: 2FUU; DIDO1 PDB: 4L7X; ING1 PDB: 2QIC; ING4 PDB: 2PNX/2VNF; ING5 PDB: 3C6W; KMT2E PDB: 4L58; PHF2 PDB: 3KQI; PHF13 PDB: 3O7A; UHRF1 PDB: 3SOW). Consensus Cys4–His–Cys3 positions are highlighted in grey and indicated on top. Locations of the secondary structure elements of TAF3-PHD are indicated on top. S880 and A902 are highlighted in purple, while P881 and W894 are highlighted in yellow.

    Journal: Nucleic Acids Research

    Article Title: Molecular determinants for recognition of serotonylated chromatin

    doi: 10.1093/nar/gkaf612

    Figure Lengend Snippet: Taf3-PHD P881 and W894 form key interaction surface with the serotonin group. ( A ) ITC analysis of GST-tagged Taf3-PHD mutants, BPTF-PHD , PHF2-PHD, or PHF8-PHD with the peptides H3K4me3 (in yellow) and H3K4me3Q5ser (in blue). Top panels display the raw heat change per injection of H3 peptide. Bottom panels represent the binding isotherm. The solid line represents the best fit to the one-set-of-sites model using MicroCal-ITC Origin 7 software. ( B ) Multiple sequence alignment (MSA) of human PHD fingers for which high-resolution structures in complex with H3K4me3 are available (ASH1L PDB: 8VLF; BPTF(2) PDB: 2FUU; DIDO1 PDB: 4L7X; ING1 PDB: 2QIC; ING4 PDB: 2PNX/2VNF; ING5 PDB: 3C6W; KMT2E PDB: 4L58; PHF2 PDB: 3KQI; PHF13 PDB: 3O7A; UHRF1 PDB: 3SOW). Consensus Cys4–His–Cys3 positions are highlighted in grey and indicated on top. Locations of the secondary structure elements of TAF3-PHD are indicated on top. S880 and A902 are highlighted in purple, while P881 and W894 are highlighted in yellow.

    Article Snippet: ITC data were subsequently analysed and fitted with the one-site binding model in the MicroCal ITC Origin Analysis software 7.0 (Table , Figs and , , and ).

    Techniques: Injection, Binding Assay, Software, Sequencing