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four-parameter dose−response fit function graphpad prism6  (GraphPad Software Inc)


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    GraphPad Software Inc four-parameter dose−response fit function graphpad prism6
    Four Parameter Dose−Response Fit Function Graphpad Prism6, supplied by GraphPad Software Inc, 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/four-parameter+dose-response+function/prism+6/pm33476150-149-16-15
    Average 90 stars, based on 1 article reviews
    four-parameter dose−response fit function graphpad prism6 - by Bioz Stars, 2026-09
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    Article Title: Phosphorylation of myelin regulatory factor by PRKG2 mediates demyelination in Huntington's disease
    Article Snippet: The data meet the assumptions of the statistical test. we have included the tests in the text as follows: Prism6 (GraphPad Software) was used for statistical analysis.

    Article Title: Small-molecule inhibitors reveal an indispensable scaffolding role of RIPK2 in NOD2 signaling APPENDIX
    Article Snippet: Statistical analysis and calculation of IC 50 values was performed using Prism 6 (GraphPad Software).

    Article Title: Method for preparing recombinant human nerve growth factor
    Article Snippet: After mixing, OD450 values were read using a microplate reader, data analysis and graphing were performed using GraphPad Prism6, and EC50 values were calculated.


    Software:

    Article Title: Permanent magnetic droplet-derived microrobots.
    Article Snippet: .. All statistical analyses of the experimental data were performed using Origin 2023b (OriginLab Co., Northampton, MA) and Prism 6 (GraphPad Inc.) software. ..


    Article Title: The Deubiquitinase USP36 Funtions Through Catalytic-Dependent and Catalytic-Independent Mechanisms in Drosophila.
    Article Snippet: .. Statistical analyses were performed using the GraphPad Prism6 software. ..

    Concentration Assay:

    Article Title: Oxidative Desymmetrization Enables the Concise Synthesis of a trans-Cyclooctene Linker for Bioorthogonal Bond Cleavage
    Article Snippet: .. Data was analyzed by fitting an exponential decay using Prism 6 (Graphpad) and the resulting pseudo-first-order rate constants were divided by the TCO concentration to calculate the second-order rate constants (Table S1). .. Data was analyzed by fitting an exponential decay using Prism 6 (Graphpad) and the resulting pseudo-first-order rate constants were divided by the TCO concentration to calculate the second-order rate constants (Table S1).



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    vmab-mIL22 exhibits dual functionality, and the functional integrity of the cytokine payloads is preserved. (A, B) Biacore sensorgrams of the interaction of vmab with mIL17A and BIAcore sensorgrams of the interaction of vmab-mIL22 with mIL17A. vmab-mIL22 retained a high affinity for the cognate antigen, similar to that of the parental antibody Vmab, which was confirmed by surface plasmon resonance analysis. Sensorgrams display the response values at IL17A concentrations of 0.01 to 0.2 μg/mL, with a CM5 chip and capture with 100 RU vmab or vmab-mIL22. The equilibrium dissociation constant (K D ) was calculated using k d /k a for each measurement. k d , dissociation rate constant or off-rate constant; k a , association rate constant or on-rate constant. Binding was biphasic, and the data were fit with heterogeneous ligand models. (C) In vitro inhibition of functional activity by vmab-mIL22. Inhibition of Groα release from HT-29 cells as a measure of IL-17A inhibition. HT29 cells were stimulated with IL-17A (5 nM) in the presence of various concentrations of vmab-mIL22. vmab was used as a positive control. Groα levels in the supernatants were measured by ELISA from R&D systems. (D) Western blot analysis of STAT3 phosphorylation (p-STAT3) induced by 10 nM vmab-hIL22 in HepG2 cells at different times. (E) Western blot analysis of STAT3 phosphorylation (p-STAT3) induced by 10 nM mIL-22Fc or vmab-mIL22 in HepG2 cells at 1.5 h Serum-starved cells (3×10 6 /mL) were stimulated with PBS, 10 nM mIL22-Fc or Vmab-mIL22 for 1.5 h at 37°C. Whole-cell lysates were resolved on denaturing gels, transferred, and immunoblotted with a polyclonal anti-phospho-STAT3 antibody.

    Journal: Frontiers in Immunology

    Article Title: A Novel Bifunctional Fusion Protein, Vunakizumab-IL22, for Protection Against Pulmonary Immune Injury Caused by Influenza Virus

    doi: 10.3389/fimmu.2021.727941

    Figure Lengend Snippet: vmab-mIL22 exhibits dual functionality, and the functional integrity of the cytokine payloads is preserved. (A, B) Biacore sensorgrams of the interaction of vmab with mIL17A and BIAcore sensorgrams of the interaction of vmab-mIL22 with mIL17A. vmab-mIL22 retained a high affinity for the cognate antigen, similar to that of the parental antibody Vmab, which was confirmed by surface plasmon resonance analysis. Sensorgrams display the response values at IL17A concentrations of 0.01 to 0.2 μg/mL, with a CM5 chip and capture with 100 RU vmab or vmab-mIL22. The equilibrium dissociation constant (K D ) was calculated using k d /k a for each measurement. k d , dissociation rate constant or off-rate constant; k a , association rate constant or on-rate constant. Binding was biphasic, and the data were fit with heterogeneous ligand models. (C) In vitro inhibition of functional activity by vmab-mIL22. Inhibition of Groα release from HT-29 cells as a measure of IL-17A inhibition. HT29 cells were stimulated with IL-17A (5 nM) in the presence of various concentrations of vmab-mIL22. vmab was used as a positive control. Groα levels in the supernatants were measured by ELISA from R&D systems. (D) Western blot analysis of STAT3 phosphorylation (p-STAT3) induced by 10 nM vmab-hIL22 in HepG2 cells at different times. (E) Western blot analysis of STAT3 phosphorylation (p-STAT3) induced by 10 nM mIL-22Fc or vmab-mIL22 in HepG2 cells at 1.5 h Serum-starved cells (3×10 6 /mL) were stimulated with PBS, 10 nM mIL22-Fc or Vmab-mIL22 for 1.5 h at 37°C. Whole-cell lysates were resolved on denaturing gels, transferred, and immunoblotted with a polyclonal anti-phospho-STAT3 antibody.

    Article Snippet: The mean values of repeated wells were plotted and the standard deviation was calculated using the four parameter dose response inhibition function in Graphpad prism.

    Techniques: Functional Assay, SPR Assay, Binding Assay, In Vitro, Inhibition, Activity Assay, Positive Control, Enzyme-linked Immunosorbent Assay, Western Blot, Phospho-proteomics