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Diagnostica Stago fluorogenic substrate zggr amc
Fluorogenic Substrate Zggr Amc, supplied by Diagnostica Stago, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorogenic+assay/fluorogenic+substrate/pmc13054078-55-15-22
Average 86 stars, based on 1 article reviews
fluorogenic substrate zggr amc - by Bioz Stars, 2026-11
86/100 stars

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Related Articles

other:

Article Title: Role of Rubicon in platelets: a promoter of thrombosis but not an autophagy repressor
Article Snippet: The thrombin generation reaction was initiated by adding a mixture of calcium and fluorogenic thrombin substrate (FluCa; 1:47; Diagnostica Stago, catalog no. 86197).

Article Title: Distinct pathogenic mechanisms underlying two protein C variants (p.Arg211Gln and p.Val367Met) in a thrombophilic family: integrated functional and structural analyses
Article Snippet: Reactions were initiated by PPP-Reagent (5 pM tissue factor and 4 μM phospholipids) (Cat. No.:86193, Diagnostica Stago, France) and monitored in real time using a fluorogenic substrate (FluCa) (Cat. No.:86197, Diagnostica Stago, France) on the CAT system.

Article Title: Distinct pathogenic mechanisms underlying two protein C variants (p.Arg211Gln and p.Val367Met) in a thrombophilic family: integrated functional and structural analyses.
Article Snippet: TG was triggered by 5 pM tissue factor and 4 μM phospholipids, and measured by monitoring the hydrolysis of a fluorogenic substrate (FluCa, AR TIC LE IN PR ES S Diagnostica Stago).

Article Title: Distinct pathogenic mechanisms underlying two protein C variants (p.Arg211Gln and p.Val367Met) in a thrombophilic family: integrated functional and structural analyses
Article Snippet: TG was triggered by 5 pM tissue factor and 4 μM phospholipids, and measured by monitoring the hydrolysis of a fluorogenic substrate (FluCa, Diagnostica Stago).

Article Title: Anthropometric measures of obesity and thrombin generation: Results from the ELSA-Brasil cohort.
Article Snippet: Background: The mechanistic link between obesity and venous thromboembolism (VTE) remains poorly understood.. The thrombin generation assay (TGA) can be used as a biomarker for hypercoagulability in obesity, which is a key mechanism in VTE pathogenesis.. However, data on obesity measures and TGA at population level are scarce and limited to Western countries.

Article Title: Distinct pathogenic mechanisms underlying two protein C variants (p.Arg211Gln and p.Val367Met) in a thrombophilic family: integrated functional and structural analyses.
Article Snippet: Reactions AR TIC LE IN PR ES S were initiated by PPP-Reagent Low (1 pM tissue factor and 4 μM phospholipids) (Cat. No.:86194, Diagnostica Stago, France) and monitored in real time using a fluorogenic substrate (FluCa) (Cat. No.:86197, Diagnostica Stago, France) on the CAT system.

Incubation:

Article Title: Screening chemical libraries for the development of oral treatments for bleeding disorders
Article Snippet: .. Plates were incubated for 10 minutes at 37°C in the automated fluorimeter before adding the fluorogenic substrate (ZGGR-AMC) and calcium (FluCa kit, Diagnostica Stago). .. Raw data were analyzed using the Thrombinoscope version 5.0 software (Thrombinoscope BV).

Article Title: Screening chemical libraries for the development of oral treatments in bleeding disorders
Article Snippet: .. Plates were incubated for 10 min at 37°C in the automated fluorimeter before adding the fluorogenic substrate (ZGGRAMC) and calcium (FluCa Kit®, Diagnostica Stago). .. Raw data were analyzed using the Thrombinoscope v.5.0 software (Thrombinoscope BV).

Automated:

Article Title: Screening chemical libraries for the development of oral treatments for bleeding disorders
Article Snippet: .. Plates were incubated for 10 minutes at 37°C in the automated fluorimeter before adding the fluorogenic substrate (ZGGR-AMC) and calcium (FluCa kit, Diagnostica Stago). .. Raw data were analyzed using the Thrombinoscope version 5.0 software (Thrombinoscope BV).



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OB uptake of T47D EVs is highest at 24 h. (A) Workflow schematic illustrating OB exposure to T47D-EV preconditioning. (B) Representative NTA histogram of concentration and size distribution of EVs remaining in the culture media of T47D EV-treated OBs at 0, 6, 12, and 24 h (n = 3). (C) Representative NTA histogram of concentration and size distribution of EVs in the culture media of OBs cultured in TBBM at 6, 12, and 24 h (n = 3). (D) Representative images of T47D-EV uptake after 24 h with nuclei of OBs stained with DAPI (blue), the cytoplasm of OBs stained with CFSE (green), and pre-stained T47D EVs internalized within OBs stained with MemGlow (magenta). Scale bar represents 50 µm.

Journal: Frontiers in Pharmacology

Article Title: Extracellular vesicle-mediated preconditioning of osteoblasts by ER+ breast cancer cells: implications for the bone metastatic niche

doi: 10.3389/fphar.2026.1844422

Figure Lengend Snippet: OB uptake of T47D EVs is highest at 24 h. (A) Workflow schematic illustrating OB exposure to T47D-EV preconditioning. (B) Representative NTA histogram of concentration and size distribution of EVs remaining in the culture media of T47D EV-treated OBs at 0, 6, 12, and 24 h (n = 3). (C) Representative NTA histogram of concentration and size distribution of EVs in the culture media of OBs cultured in TBBM at 6, 12, and 24 h (n = 3). (D) Representative images of T47D-EV uptake after 24 h with nuclei of OBs stained with DAPI (blue), the cytoplasm of OBs stained with CFSE (green), and pre-stained T47D EVs internalized within OBs stained with MemGlow (magenta). Scale bar represents 50 µm.

Article Snippet: EVs were fluorescently labeled with MemGlow (Cytoskeleton, MG04) at a final concentration of 0.2 μM and incubated for 20 min at room temperature in Protein LoBind tubes (Eppendorf, 0030108116).

Techniques: Concentration Assay, Cell Culture, Staining