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exponential decay equation graphpad v. 9.1.2  (GraphPad Software Inc)


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    GraphPad Software Inc exponential decay equation graphpad v. 9.1.2
    a Fibrin dissolved by the fibrinolytic nanocage (FNC) was monitored by measuring the height of the remaining gel after predetermined lengths of time (0, 0.5, 1, 2, 4, 6, 8, 10, 12, or 24 h). Tris-based saline buffer (TBS) and urokinase (uPA) were used as controls. b The relative decrease in height of the fibrin gels was plotted. The results are presented as the means ± SD ( n = 3 independent experiments), and each line was obtained from the <t>exponential</t> decay equation model as described in the Methods. c To monitor nanoparticle transport across the fibrin gel upon fibrinolysis, a Transwell assay was performed. FNCs and wild-type ferritin nanocages (wFTHs) were placed on the upper chamber of the Transwell plate. The bottom chamber contained only FNC in TBS. d The wFTH transported to the bottom chamber was analyzed by western blot. e The relative intensity of the transported wFTH to the applied wFTH was plotted.
    Exponential Decay Equation Graphpad V. 9.1.2, 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/exponential+decay+equation+graphpad+v%2E+9%2E1%2E2/exponential+decay+equation+graphpad+v++9+1+2/pmc08569170-58-10-13
    Average 90 stars, based on 1 article reviews
    exponential decay equation graphpad v. 9.1.2 - by Bioz Stars, 2026-09
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    1) Product Images from "Fibrinolytic nanocages dissolve clots in the tumor microenvironment, improving the distribution and therapeutic efficacy of anticancer drugs"

    Article Title: Fibrinolytic nanocages dissolve clots in the tumor microenvironment, improving the distribution and therapeutic efficacy of anticancer drugs

    Journal: Experimental & Molecular Medicine

    doi: 10.1038/s12276-021-00688-7

    a Fibrin dissolved by the fibrinolytic nanocage (FNC) was monitored by measuring the height of the remaining gel after predetermined lengths of time (0, 0.5, 1, 2, 4, 6, 8, 10, 12, or 24 h). Tris-based saline buffer (TBS) and urokinase (uPA) were used as controls. b The relative decrease in height of the fibrin gels was plotted. The results are presented as the means ± SD ( n = 3 independent experiments), and each line was obtained from the exponential decay equation model as described in the Methods. c To monitor nanoparticle transport across the fibrin gel upon fibrinolysis, a Transwell assay was performed. FNCs and wild-type ferritin nanocages (wFTHs) were placed on the upper chamber of the Transwell plate. The bottom chamber contained only FNC in TBS. d The wFTH transported to the bottom chamber was analyzed by western blot. e The relative intensity of the transported wFTH to the applied wFTH was plotted.
    Figure Legend Snippet: a Fibrin dissolved by the fibrinolytic nanocage (FNC) was monitored by measuring the height of the remaining gel after predetermined lengths of time (0, 0.5, 1, 2, 4, 6, 8, 10, 12, or 24 h). Tris-based saline buffer (TBS) and urokinase (uPA) were used as controls. b The relative decrease in height of the fibrin gels was plotted. The results are presented as the means ± SD ( n = 3 independent experiments), and each line was obtained from the exponential decay equation model as described in the Methods. c To monitor nanoparticle transport across the fibrin gel upon fibrinolysis, a Transwell assay was performed. FNCs and wild-type ferritin nanocages (wFTHs) were placed on the upper chamber of the Transwell plate. The bottom chamber contained only FNC in TBS. d The wFTH transported to the bottom chamber was analyzed by western blot. e The relative intensity of the transported wFTH to the applied wFTH was plotted.

    Techniques Used: Saline, Transwell Assay, Western Blot

    Fibrin decay parameters using the exponential decay equation.
    Figure Legend Snippet: Fibrin decay parameters using the exponential decay equation.

    Techniques Used: Saline

    Related Articles

    Saline:

    Article Title: Fibrinolytic nanocages dissolve clots in the tumor microenvironment, improving the distribution and therapeutic efficacy of anticancer drugs
    Article Snippet: Tris-based saline buffer (TBS; 20 mM Tris-HCl pH 8.0, 150 mM NaCl) was used as a control. .. The fibrin decay of each sample was analyzed using the exponential decay equation (GraphPad v. 9.1.2). .. The equation is described as Y = (Y0 − Plateau) × exp (−K × X) + Plateau, where Y0 is the decay value (

    Transwell Assay:

    Article Title: Fibrinolytic nanocages dissolve clots in the tumor microenvironment, improving the distribution and therapeutic efficacy of anticancer drugs
    Article Snippet: Tris-based saline buffer (TBS; 20 mM Tris-HCl pH 8.0, 150 mM NaCl) was used as a control. .. The fibrin decay of each sample was analyzed using the exponential decay equation (GraphPad v. 9.1.2). .. The equation is described as Y = (Y0 − Plateau) × exp (−K × X) + Plateau, where Y0 is the decay value (

    Western Blot:

    Article Title: Fibrinolytic nanocages dissolve clots in the tumor microenvironment, improving the distribution and therapeutic efficacy of anticancer drugs
    Article Snippet: Tris-based saline buffer (TBS; 20 mM Tris-HCl pH 8.0, 150 mM NaCl) was used as a control. .. The fibrin decay of each sample was analyzed using the exponential decay equation (GraphPad v. 9.1.2). .. The equation is described as Y = (Y0 − Plateau) × exp (−K × X) + Plateau, where Y0 is the decay value (



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    exponential decay equation graphpad v. 9.1.2  (GraphPad Software Inc)
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    GraphPad Software Inc exponential decay equation graphpad v. 9.1.2
    a Fibrin dissolved by the fibrinolytic nanocage (FNC) was monitored by measuring the height of the remaining gel after predetermined lengths of time (0, 0.5, 1, 2, 4, 6, 8, 10, 12, or 24 h). Tris-based saline buffer (TBS) and urokinase (uPA) were used as controls. b The relative decrease in height of the fibrin gels was plotted. The results are presented as the means ± SD ( n = 3 independent experiments), and each line was obtained from the <t>exponential</t> decay equation model as described in the Methods. c To monitor nanoparticle transport across the fibrin gel upon fibrinolysis, a Transwell assay was performed. FNCs and wild-type ferritin nanocages (wFTHs) were placed on the upper chamber of the Transwell plate. The bottom chamber contained only FNC in TBS. d The wFTH transported to the bottom chamber was analyzed by western blot. e The relative intensity of the transported wFTH to the applied wFTH was plotted.
    Exponential Decay Equation Graphpad V. 9.1.2, 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/exponential+decay+equation+graphpad+v%2E+9%2E1%2E2/exponential+decay+equation+graphpad+v++9+1+2/pmc08569170-58-10-13
    Average 90 stars, based on 1 article reviews
    exponential decay equation graphpad v. 9.1.2 - by Bioz Stars, 2026-09
    90/100 stars
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    a Fibrin dissolved by the fibrinolytic nanocage (FNC) was monitored by measuring the height of the remaining gel after predetermined lengths of time (0, 0.5, 1, 2, 4, 6, 8, 10, 12, or 24 h). Tris-based saline buffer (TBS) and urokinase (uPA) were used as controls. b The relative decrease in height of the fibrin gels was plotted. The results are presented as the means ± SD ( n = 3 independent experiments), and each line was obtained from the exponential decay equation model as described in the Methods. c To monitor nanoparticle transport across the fibrin gel upon fibrinolysis, a Transwell assay was performed. FNCs and wild-type ferritin nanocages (wFTHs) were placed on the upper chamber of the Transwell plate. The bottom chamber contained only FNC in TBS. d The wFTH transported to the bottom chamber was analyzed by western blot. e The relative intensity of the transported wFTH to the applied wFTH was plotted.

    Journal: Experimental & Molecular Medicine

    Article Title: Fibrinolytic nanocages dissolve clots in the tumor microenvironment, improving the distribution and therapeutic efficacy of anticancer drugs

    doi: 10.1038/s12276-021-00688-7

    Figure Lengend Snippet: a Fibrin dissolved by the fibrinolytic nanocage (FNC) was monitored by measuring the height of the remaining gel after predetermined lengths of time (0, 0.5, 1, 2, 4, 6, 8, 10, 12, or 24 h). Tris-based saline buffer (TBS) and urokinase (uPA) were used as controls. b The relative decrease in height of the fibrin gels was plotted. The results are presented as the means ± SD ( n = 3 independent experiments), and each line was obtained from the exponential decay equation model as described in the Methods. c To monitor nanoparticle transport across the fibrin gel upon fibrinolysis, a Transwell assay was performed. FNCs and wild-type ferritin nanocages (wFTHs) were placed on the upper chamber of the Transwell plate. The bottom chamber contained only FNC in TBS. d The wFTH transported to the bottom chamber was analyzed by western blot. e The relative intensity of the transported wFTH to the applied wFTH was plotted.

    Article Snippet: The fibrin decay of each sample was analyzed using the exponential decay equation (GraphPad v. 9.1.2).

    Techniques: Saline, Transwell Assay, Western Blot

    Fibrin decay parameters using the exponential decay equation.

    Journal: Experimental & Molecular Medicine

    Article Title: Fibrinolytic nanocages dissolve clots in the tumor microenvironment, improving the distribution and therapeutic efficacy of anticancer drugs

    doi: 10.1038/s12276-021-00688-7

    Figure Lengend Snippet: Fibrin decay parameters using the exponential decay equation.

    Article Snippet: The fibrin decay of each sample was analyzed using the exponential decay equation (GraphPad v. 9.1.2).

    Techniques: Saline