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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/type+i+collagen+horm/kollagenreagens+horm/us12208132-235-0-5
    Average 90 stars, based on 1 article reviews
    collagen type i fibrils kollagenreagens-horm - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Fluorescence:

    Article Title: Heat Shock Protein 90 Inhibitors Reduce Trafficking of ATP-gated P2X1 Receptors and Human Platelet Responsiveness
    Article Snippet: .. Ratiometric fluorescence measurements were conducted at 37 °C in a Cairn spectrofluorometer system (Cairn Research Limited, Faversham, Kent, UK) in response to 1 μ m α,β-meATP, 1 μ m ADP, or 0.5 μg ml −1 type I collagen horm (Nycomed, Austria) following 1-min or 20-min incubation with 2 μ m geldanamycin, 1 μg ml −1 radicicol, or 0.2% dimethyl sulfoxide. ..

    Incubation:

    Article Title: Heat Shock Protein 90 Inhibitors Reduce Trafficking of ATP-gated P2X1 Receptors and Human Platelet Responsiveness
    Article Snippet: .. Ratiometric fluorescence measurements were conducted at 37 °C in a Cairn spectrofluorometer system (Cairn Research Limited, Faversham, Kent, UK) in response to 1 μ m α,β-meATP, 1 μ m ADP, or 0.5 μg ml −1 type I collagen horm (Nycomed, Austria) following 1-min or 20-min incubation with 2 μ m geldanamycin, 1 μg ml −1 radicicol, or 0.2% dimethyl sulfoxide. ..

    Article Title: Monocytes downregulate the early stage of collagen-induced platelet activation by a PECAM-1-dependent mechanism.
    Article Snippet: Background: Blood vessel damage results in exposure of the subendothelial matrix, to which platelets adhere.. Monocytes are recruited and activated at the site of injury.. Objectives:Here we studied the effect of monocytes on platelet activation induced by exposure to fibrillar collagen.



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    (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