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93
Innovative Research Inc plasminogen
SDS-PAGE analysis of porcine <t>plasminogen</t> activation by porcine uPA. Porcine plasminogen (750 nM) was incubated with porcine uPA (100 nM) in the presence of εACA (10 mM) for 0 min ( left lane ) or 30 min ( right lane ) at 25°C. Samples were taken to resolve the bands on SDS-PAGE (5–15% gradient) and quantitative densitometry was performed to estimate the proportion of plasminogen that was converted to plasmin. HC, heavy chain; LC, light chain; Pg, plasminogen.
Plasminogen, supplied by Innovative Research Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SDS-PAGE analysis of porcine plasminogen activation by porcine uPA. Porcine plasminogen (750 nM) was incubated with porcine uPA (100 nM) in the presence of εACA (10 mM) for 0 min ( left lane ) or 30 min ( right lane ) at 25°C. Samples were taken to resolve the bands on SDS-PAGE (5–15% gradient) and quantitative densitometry was performed to estimate the proportion of plasminogen that was converted to plasmin. HC, heavy chain; LC, light chain; Pg, plasminogen.

Journal: TH Open: Companion Journal to Thrombosis and Haemostasis

Article Title: Differences and Compatibility between Human and Porcine Fibrinolytic Components toward Plasmin Generation and Fibrin Degradation

doi: 10.1055/a-2777-7484

Figure Lengend Snippet: SDS-PAGE analysis of porcine plasminogen activation by porcine uPA. Porcine plasminogen (750 nM) was incubated with porcine uPA (100 nM) in the presence of εACA (10 mM) for 0 min ( left lane ) or 30 min ( right lane ) at 25°C. Samples were taken to resolve the bands on SDS-PAGE (5–15% gradient) and quantitative densitometry was performed to estimate the proportion of plasminogen that was converted to plasmin. HC, heavy chain; LC, light chain; Pg, plasminogen.

Article Snippet: Materials: Recombinant porcine tPA, recombinant porcine uPA, purified porcine fibrinogen, and purified porcine plasminogen were purchased from Innovative Research Inc (Novi, MI, USA).

Techniques: SDS Page, Activation Assay, Incubation

Rates of porcine plasmin generation by porcine (closed) or human (open) tPA. Porcine plasminogen (Pg) at varying concentration (0 to 0.75 µM) was activated by tPA (0.1 nM) in the presence of either (A) porcine or (B) human fibrin (1 µM); converted from fibrinogen using human thrombin (2 nM). The initial rates of plasmin generation were then estimated using the time-squared method and plotted with respect to the initial plasminogen concentration ( N ≥ 3).

Journal: TH Open: Companion Journal to Thrombosis and Haemostasis

Article Title: Differences and Compatibility between Human and Porcine Fibrinolytic Components toward Plasmin Generation and Fibrin Degradation

doi: 10.1055/a-2777-7484

Figure Lengend Snippet: Rates of porcine plasmin generation by porcine (closed) or human (open) tPA. Porcine plasminogen (Pg) at varying concentration (0 to 0.75 µM) was activated by tPA (0.1 nM) in the presence of either (A) porcine or (B) human fibrin (1 µM); converted from fibrinogen using human thrombin (2 nM). The initial rates of plasmin generation were then estimated using the time-squared method and plotted with respect to the initial plasminogen concentration ( N ≥ 3).

Article Snippet: Materials: Recombinant porcine tPA, recombinant porcine uPA, purified porcine fibrinogen, and purified porcine plasminogen were purchased from Innovative Research Inc (Novi, MI, USA).

Techniques: Concentration Assay

Rates of human plasmin generation by porcine (closed) or human (open) tPA. Human plasminogen (Pg) at varying concentration (0 to 0.75 µM) was activated by tPA (0.1 nM) in the presence of either (A) porcine or (B) human fibrin (1 µM); converted from fibrinogen using human thrombin (2 nM). The initial rates of plasmin generation were then estimated using the time-squared method and plotted with respect to the initial plasminogen concentration ( N ≥ 3).

Journal: TH Open: Companion Journal to Thrombosis and Haemostasis

Article Title: Differences and Compatibility between Human and Porcine Fibrinolytic Components toward Plasmin Generation and Fibrin Degradation

doi: 10.1055/a-2777-7484

Figure Lengend Snippet: Rates of human plasmin generation by porcine (closed) or human (open) tPA. Human plasminogen (Pg) at varying concentration (0 to 0.75 µM) was activated by tPA (0.1 nM) in the presence of either (A) porcine or (B) human fibrin (1 µM); converted from fibrinogen using human thrombin (2 nM). The initial rates of plasmin generation were then estimated using the time-squared method and plotted with respect to the initial plasminogen concentration ( N ≥ 3).

Article Snippet: Materials: Recombinant porcine tPA, recombinant porcine uPA, purified porcine fibrinogen, and purified porcine plasminogen were purchased from Innovative Research Inc (Novi, MI, USA).

Techniques: Concentration Assay

Similarity of amino acid sequences when compared between porcine and human plasminogen, tPA, and fibrinogen chains by domain. The heat map illustrates domains that display highest (red) to lowest (blue) similarities. The spikes highlight the domains that bind fibrinogen in a lysine-dependent manner. (Created in BioRender. Kim, P. (2025) https://BioRender.com/zvi11gx .)

Journal: TH Open: Companion Journal to Thrombosis and Haemostasis

Article Title: Differences and Compatibility between Human and Porcine Fibrinolytic Components toward Plasmin Generation and Fibrin Degradation

doi: 10.1055/a-2777-7484

Figure Lengend Snippet: Similarity of amino acid sequences when compared between porcine and human plasminogen, tPA, and fibrinogen chains by domain. The heat map illustrates domains that display highest (red) to lowest (blue) similarities. The spikes highlight the domains that bind fibrinogen in a lysine-dependent manner. (Created in BioRender. Kim, P. (2025) https://BioRender.com/zvi11gx .)

Article Snippet: Materials: Recombinant porcine tPA, recombinant porcine uPA, purified porcine fibrinogen, and purified porcine plasminogen were purchased from Innovative Research Inc (Novi, MI, USA).

Techniques: