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The concentration of intracellular fraction <t>mtPA</t> was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by <t>ELISA</t> in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.
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The concentration of intracellular fraction <t>mtPA</t> was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by <t>ELISA</t> in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.
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The concentration of intracellular fraction <t>mtPA</t> was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by <t>ELISA</t> in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.
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The concentration of intracellular fraction <t>mtPA</t> was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by <t>ELISA</t> in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.
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The concentration of intracellular fraction <t>mtPA</t> was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by <t>ELISA</t> in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.
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The concentration of intracellular fraction <t>mtPA</t> was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by <t>ELISA</t> in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.
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The concentration of intracellular fraction <t>mtPA</t> was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by <t>ELISA</t> in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.
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The concentration of intracellular fraction <t>mtPA</t> was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by <t>ELISA</t> in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.
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The concentration of intracellular fraction <t>mtPA</t> was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by <t>ELISA</t> in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.
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Select this product for Molecular Innovations name, Mouse Prothrombin Total Antigen ELISA Kit and product number, MPTKT-TOT. Mouse Total Factor II (Prothrombin) ELISA Kit from Innovative Research is intended for the quantitative determination of total
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The concentration of intracellular fraction mtPA was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by ELISA in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.

Journal: Pharmaceutical research

Article Title: A Role for Low Density Lipoprotein Receptor-related Protein 1 in the Cellular Uptake of Tissue Plasminogen Activator in the Lungs

doi: 10.1007/s11095-015-1763-6

Figure Lengend Snippet: The concentration of intracellular fraction mtPA was lower over time in the presence of LRP1 inhibitor, receptor associated protein (RAP) in primary liver and lung cell suspensions (20,000 cells each). Cells were exposed to mtPA (50ng) at time 0 in the presence or absence of RAP (400nM). Representative Western blots of intracellular fraction mtPA over time in (A) primary whole liver cell lysates and (B) primary whole lung cell lysates. These findings were corroborated by the measurement of intracellular fraction mtPA concentrations measured by ELISA in (C) liver cell (*p=0.0132 at 1 min) and (D) lung cell (*p=0.009; +p<0.001; #p=0.066) lysates as well as in extracellular fraction (supernatant) media of (E) liver (*p=0.005; +p=0.0005) and (F) lung (*p=0.024; +p=0.001) cell suspensions. Data are the mean (±S.E.M.) of 3-4 samples/group and p values were generated from post ANOVA Holm-Sidak tests.

Article Snippet: Measurement of mtPA Uptake by Lung and Liver Cell Suspensions The concentration of mtPA in lung and liver cell lysates (intracellular fraction) and supernatants (extracellular fraction) was detected using mtPA total antigen assay ELISA kit (MTPAKT-TOT, Molecular Innovations).

Techniques: Concentration Assay, Western Blot, Enzyme-linked Immunosorbent Assay, Generated