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collagen type i fibrils kollagenreagens-horm  (Nycomed)

 
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    Nycomed collagen type i fibrils kollagenreagens-horm
    Collagen Type I Fibrils Kollagenreagens Horm, supplied by Nycomed, 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/horm+collagen+type+i/kollagenreagens+horm/us12208132-235-0-5
    Average 90 stars, based on 1 article reviews
    collagen type i fibrils kollagenreagens-horm - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Activated platelets kill Staphylococcus aureus, but not Streptococcus pneumoniae-The role of FcγRIIa and platelet factor 4/heparinantibodies.
    Article Snippet: To obtain the platelet releasate, washed platelets in Tyrode’s buffer were co-stimulated with 20 μM TRAP-6 and 5 μg/ml Horm collagen type I (Nycomed, Opfikon, Luxembourg) for 15 minutes under agitation.

    Ex Vivo:

    Article Title: Reduced platelet forces underlie impaired hemostasis in mouse models of MYH9 -related disease
    Article Snippet: .. Ex vivo thrombus formation assays were performed at a wall shear rate of 1000 s −1 on collagen-passivated surfaces [Horm collagen type I (200 μg/ml) from horse tendon; Nycomed] in a microfluidic parallel platelet flow chamber (on μ-Slide VI 0.1 with the following physical dimensions: width, 1 mm; height, 100 μm; and length, 17 mm; ibidi GmbH, Germany). .. To visualize thrombus formation, before perfusion, platelets in ACD-A anticoagulated whole blood were stained with FITC-labeled anti-human CD61 antibody (clone: RUU-PL7F12; catalog no. 340715, BD Pharmingen, USA, used at final ratio 1:100).

    Shear:

    Article Title: Reduced platelet forces underlie impaired hemostasis in mouse models of MYH9 -related disease
    Article Snippet: .. Ex vivo thrombus formation assays were performed at a wall shear rate of 1000 s −1 on collagen-passivated surfaces [Horm collagen type I (200 μg/ml) from horse tendon; Nycomed] in a microfluidic parallel platelet flow chamber (on μ-Slide VI 0.1 with the following physical dimensions: width, 1 mm; height, 100 μm; and length, 17 mm; ibidi GmbH, Germany). .. To visualize thrombus formation, before perfusion, platelets in ACD-A anticoagulated whole blood were stained with FITC-labeled anti-human CD61 antibody (clone: RUU-PL7F12; catalog no. 340715, BD Pharmingen, USA, used at final ratio 1:100).

    Purification:

    Article Title: Platelet Dysfunction in Thrombosis Patients Treated with Vitamin K Antagonists and Recurrent Bleeding
    Article Snippet: Arachidonic acid was obtained from Chronolog (Havertown, PA, USA), epinephrine from Janssen Chimica (Geel, Belgium) and PAR1 peptide SFLLRN from (Bachem, Bubendorf, Switzerland). .. ADP and bovine serum albumin (BSA) came from Sigma (St. Louis, MO, USA), Horm collagen type I from Nycomed (Linz, Austria), ristocetin from American Biochemical and Pharmaceutical (Marlton, NJ, USA) and convulxin was purified from the venom of Crotalus durissus terrificus . .. Fluorescein isothiocyanate (FITC)-labeled monoclonal antibody (mAb) against platelet-bound human fibrinogen was from WAK Chemie Medical (Steinbach, Germany), allophycocyanin (APC)-labeled mouse anti-CD63 mAb from Biolegend (San Diego, CA, USA), and FITC-labeled mouse anti-CD62P mAb from Beckman Coulter (Miami, FL, USA).

    Derivative Assay:

    Article Title: Roles of Focal Adhesion Kinase PTK2 and Integrin αIIbβ3 Signaling in Collagen- and GPVI-Dependent Thrombus Formation under Shear
    Article Snippet: .. Horm collagen type I derived from equine tendon was obtained from Nycomed (Hoofddorp, The Netherlands). .. Human placenta-derived collagen type III (1230-01S) was supplied by Southern Biotechnology (Birmingham, AL, USA).



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    Image Search Results


    (a-c) Washed platelets were incubated in vitro with 10 μg/ml of the indicated antibodies for 5 min and stimulated with Horm or soluble collagen. Light transmission was recorded on an Apact four-channel aggregometer over 20 min. Representative aggregation curves of n=3, 2 independent experiments. LEN/B: anti-α2 integrin antibody51. (d, e) Flow cytometry reveals unaltered reactivity of DOM/B-treated WT platelets upon thrombin stimulation compared to WT controls. Mean ± SD. n=3 mice, 4 independent experiments, two-tailed unpaired t-test with Welch’s correction. (f) Aggregation upon thrombin-stimulation is not affected in the presence of DOM/B. Light transmission was recorded on an Apact four-channel aggregometer over 10 min. Representative curves of n=3, 3 individual experiments. (g) Thrombin exosites I and II were blocked by the aptamers HD1 and HD22, respectively. Platelets were incubated with the indicated antibody (10 μg/ml) prior to thrombin stimulation. Thrombin-mediated cleavage of GPV was assessed by flow cytometry. Mean ± SD. n=3 mice, 3 independent experiments. (h) Thrombin clotting time was assessed using a ball coagulometer in GPV mutant or anti-mGPV mAb treated PRP in the presence or absence of HD22. Antibody concentration: 10 μg/ml; aptamer concentration: 1.5 μM f.c., thrombin: 17 nM. Mean ± SD. WT, WT+DOM/B, WT+DOM/C: n=5, Gp5−/−: n=4, Gp5dThr, Gp5−/−+HD22, Gp5dThr+HD22: n=3, WT+DOM/B+HD22, WT+DOM/C+HD22: n=6, WT+HD22: n=8. One-way ANOVA followed by Dunn’s test for multiple comparisons.

    Journal: Nature cardiovascular research

    Article Title: Platelet glycoprotein V spatio-temporally controls fibrin formation

    doi: 10.1038/s44161-023-00254-6

    Figure Lengend Snippet: (a-c) Washed platelets were incubated in vitro with 10 μg/ml of the indicated antibodies for 5 min and stimulated with Horm or soluble collagen. Light transmission was recorded on an Apact four-channel aggregometer over 20 min. Representative aggregation curves of n=3, 2 independent experiments. LEN/B: anti-α2 integrin antibody51. (d, e) Flow cytometry reveals unaltered reactivity of DOM/B-treated WT platelets upon thrombin stimulation compared to WT controls. Mean ± SD. n=3 mice, 4 independent experiments, two-tailed unpaired t-test with Welch’s correction. (f) Aggregation upon thrombin-stimulation is not affected in the presence of DOM/B. Light transmission was recorded on an Apact four-channel aggregometer over 10 min. Representative curves of n=3, 3 individual experiments. (g) Thrombin exosites I and II were blocked by the aptamers HD1 and HD22, respectively. Platelets were incubated with the indicated antibody (10 μg/ml) prior to thrombin stimulation. Thrombin-mediated cleavage of GPV was assessed by flow cytometry. Mean ± SD. n=3 mice, 3 independent experiments. (h) Thrombin clotting time was assessed using a ball coagulometer in GPV mutant or anti-mGPV mAb treated PRP in the presence or absence of HD22. Antibody concentration: 10 μg/ml; aptamer concentration: 1.5 μM f.c., thrombin: 17 nM. Mean ± SD. WT, WT+DOM/B, WT+DOM/C: n=5, Gp5−/−: n=4, Gp5dThr, Gp5−/−+HD22, Gp5dThr+HD22: n=3, WT+DOM/B+HD22, WT+DOM/C+HD22: n=6, WT+HD22: n=8. One-way ANOVA followed by Dunn’s test for multiple comparisons.

    Article Snippet: Fibrillar type I collagen (Horm) was from Takeda, Rhodocytin was provided by Johannes Eble (University of Münster, Münster, Germany).

    Techniques: In Vitro, Incubation, Transmission Assay, Flow Cytometry, Two Tailed Test, Coagulation, Mutagenesis, Concentration Assay