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alexa fluor 488 conjugated mouse anti human cd61  (Bio-Rad)


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    Bio-Rad alexa fluor 488 conjugated mouse anti human cd61
    In Vitro Assessment of Platelet Reactivity by Aggregometry and MF (A) Percent maximal aggregation of platelets from patients on dual antiplatelet therapy (DAPT) (n = 27) in response to adenosine diphosphate (ADP) (20 μmol/L) and TRAP-6 (10 μmol/L). Results are compared with healthy donors (n = 15). (B) Mean fluorescence intensity (FI) (n = 8 clotting events per individual) of accumulated platelets from whole blood of healthy donors vs patients on DAPT using a PDMS (polydimethylsiloxane) device attached to a type I equine collagen–coated glass slide. Digital imagines were captured using an automated fluorescent microscope system ( t = 900 seconds). (C) Photomicrograph of a fabricated collagen-coated chip and deposition of platelets labeled with Alexa Fluor 488–conjugated mouse anti-human <t>CD61</t> from healthy donors or DAPT-treated patients ( t = 900 seconds). (D) Mean platelet FI (n = 8 clotting events per individual) of accumulated platelets from WB of the same individuals from using collagen-coated chips and an integrated microfluidic (MF) device. (E) Maximal thrombus area (μm 2 ) occupied by calcein-labeled platelets from healthy donors vs patients (n = 10 mice per group, 10 individuals for each of the 2 groups, 3 arteriole injuries per mouse). The central box represents the values between the 10th and 90th percentiles, and the middle line is the mean. Statistical significance was determined using Mann-Whitney U test. ∗∗∗ P < 0.001 relative to healthy donors; ∗∗∗ P < 0.001 ADP relative to TRAP-6 for patients on DAPT.
    Alexa Fluor 488 Conjugated Mouse Anti Human Cd61, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 36 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Preclinical Efficacy of a Hemostatic Agent in Overcoming Dual Antiplatelet Therapy"

    Article Title: Preclinical Efficacy of a Hemostatic Agent in Overcoming Dual Antiplatelet Therapy

    Journal: JACC: Basic to Translational Science

    doi: 10.1016/j.jacbts.2025.101356

    In Vitro Assessment of Platelet Reactivity by Aggregometry and MF (A) Percent maximal aggregation of platelets from patients on dual antiplatelet therapy (DAPT) (n = 27) in response to adenosine diphosphate (ADP) (20 μmol/L) and TRAP-6 (10 μmol/L). Results are compared with healthy donors (n = 15). (B) Mean fluorescence intensity (FI) (n = 8 clotting events per individual) of accumulated platelets from whole blood of healthy donors vs patients on DAPT using a PDMS (polydimethylsiloxane) device attached to a type I equine collagen–coated glass slide. Digital imagines were captured using an automated fluorescent microscope system ( t = 900 seconds). (C) Photomicrograph of a fabricated collagen-coated chip and deposition of platelets labeled with Alexa Fluor 488–conjugated mouse anti-human CD61 from healthy donors or DAPT-treated patients ( t = 900 seconds). (D) Mean platelet FI (n = 8 clotting events per individual) of accumulated platelets from WB of the same individuals from using collagen-coated chips and an integrated microfluidic (MF) device. (E) Maximal thrombus area (μm 2 ) occupied by calcein-labeled platelets from healthy donors vs patients (n = 10 mice per group, 10 individuals for each of the 2 groups, 3 arteriole injuries per mouse). The central box represents the values between the 10th and 90th percentiles, and the middle line is the mean. Statistical significance was determined using Mann-Whitney U test. ∗∗∗ P < 0.001 relative to healthy donors; ∗∗∗ P < 0.001 ADP relative to TRAP-6 for patients on DAPT.
    Figure Legend Snippet: In Vitro Assessment of Platelet Reactivity by Aggregometry and MF (A) Percent maximal aggregation of platelets from patients on dual antiplatelet therapy (DAPT) (n = 27) in response to adenosine diphosphate (ADP) (20 μmol/L) and TRAP-6 (10 μmol/L). Results are compared with healthy donors (n = 15). (B) Mean fluorescence intensity (FI) (n = 8 clotting events per individual) of accumulated platelets from whole blood of healthy donors vs patients on DAPT using a PDMS (polydimethylsiloxane) device attached to a type I equine collagen–coated glass slide. Digital imagines were captured using an automated fluorescent microscope system ( t = 900 seconds). (C) Photomicrograph of a fabricated collagen-coated chip and deposition of platelets labeled with Alexa Fluor 488–conjugated mouse anti-human CD61 from healthy donors or DAPT-treated patients ( t = 900 seconds). (D) Mean platelet FI (n = 8 clotting events per individual) of accumulated platelets from WB of the same individuals from using collagen-coated chips and an integrated microfluidic (MF) device. (E) Maximal thrombus area (μm 2 ) occupied by calcein-labeled platelets from healthy donors vs patients (n = 10 mice per group, 10 individuals for each of the 2 groups, 3 arteriole injuries per mouse). The central box represents the values between the 10th and 90th percentiles, and the middle line is the mean. Statistical significance was determined using Mann-Whitney U test. ∗∗∗ P < 0.001 relative to healthy donors; ∗∗∗ P < 0.001 ADP relative to TRAP-6 for patients on DAPT.

    Techniques Used: In Vitro, Fluorescence, Coagulation, Microscopy, Labeling, MANN-WHITNEY



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    In Vitro Assessment of Platelet Reactivity by Aggregometry and MF (A) Percent maximal aggregation of platelets from patients on dual antiplatelet therapy (DAPT) (n = 27) in response to adenosine diphosphate (ADP) (20 μmol/L) and TRAP-6 (10 μmol/L). Results are compared with healthy donors (n = 15). (B) Mean fluorescence intensity (FI) (n = 8 clotting events per individual) of accumulated platelets from whole blood of healthy donors vs patients on DAPT using a PDMS (polydimethylsiloxane) device attached to a type I equine collagen–coated glass slide. Digital imagines were captured using an automated fluorescent microscope system ( t = 900 seconds). (C) Photomicrograph of a fabricated collagen-coated chip and deposition of platelets labeled with Alexa Fluor 488–conjugated mouse anti-human <t>CD61</t> from healthy donors or DAPT-treated patients ( t = 900 seconds). (D) Mean platelet FI (n = 8 clotting events per individual) of accumulated platelets from WB of the same individuals from using collagen-coated chips and an integrated microfluidic (MF) device. (E) Maximal thrombus area (μm 2 ) occupied by calcein-labeled platelets from healthy donors vs patients (n = 10 mice per group, 10 individuals for each of the 2 groups, 3 arteriole injuries per mouse). The central box represents the values between the 10th and 90th percentiles, and the middle line is the mean. Statistical significance was determined using Mann-Whitney U test. ∗∗∗ P < 0.001 relative to healthy donors; ∗∗∗ P < 0.001 ADP relative to TRAP-6 for patients on DAPT.
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    Image Search Results


    In Vitro Assessment of Platelet Reactivity by Aggregometry and MF (A) Percent maximal aggregation of platelets from patients on dual antiplatelet therapy (DAPT) (n = 27) in response to adenosine diphosphate (ADP) (20 μmol/L) and TRAP-6 (10 μmol/L). Results are compared with healthy donors (n = 15). (B) Mean fluorescence intensity (FI) (n = 8 clotting events per individual) of accumulated platelets from whole blood of healthy donors vs patients on DAPT using a PDMS (polydimethylsiloxane) device attached to a type I equine collagen–coated glass slide. Digital imagines were captured using an automated fluorescent microscope system ( t = 900 seconds). (C) Photomicrograph of a fabricated collagen-coated chip and deposition of platelets labeled with Alexa Fluor 488–conjugated mouse anti-human CD61 from healthy donors or DAPT-treated patients ( t = 900 seconds). (D) Mean platelet FI (n = 8 clotting events per individual) of accumulated platelets from WB of the same individuals from using collagen-coated chips and an integrated microfluidic (MF) device. (E) Maximal thrombus area (μm 2 ) occupied by calcein-labeled platelets from healthy donors vs patients (n = 10 mice per group, 10 individuals for each of the 2 groups, 3 arteriole injuries per mouse). The central box represents the values between the 10th and 90th percentiles, and the middle line is the mean. Statistical significance was determined using Mann-Whitney U test. ∗∗∗ P < 0.001 relative to healthy donors; ∗∗∗ P < 0.001 ADP relative to TRAP-6 for patients on DAPT.

    Journal: JACC: Basic to Translational Science

    Article Title: Preclinical Efficacy of a Hemostatic Agent in Overcoming Dual Antiplatelet Therapy

    doi: 10.1016/j.jacbts.2025.101356

    Figure Lengend Snippet: In Vitro Assessment of Platelet Reactivity by Aggregometry and MF (A) Percent maximal aggregation of platelets from patients on dual antiplatelet therapy (DAPT) (n = 27) in response to adenosine diphosphate (ADP) (20 μmol/L) and TRAP-6 (10 μmol/L). Results are compared with healthy donors (n = 15). (B) Mean fluorescence intensity (FI) (n = 8 clotting events per individual) of accumulated platelets from whole blood of healthy donors vs patients on DAPT using a PDMS (polydimethylsiloxane) device attached to a type I equine collagen–coated glass slide. Digital imagines were captured using an automated fluorescent microscope system ( t = 900 seconds). (C) Photomicrograph of a fabricated collagen-coated chip and deposition of platelets labeled with Alexa Fluor 488–conjugated mouse anti-human CD61 from healthy donors or DAPT-treated patients ( t = 900 seconds). (D) Mean platelet FI (n = 8 clotting events per individual) of accumulated platelets from WB of the same individuals from using collagen-coated chips and an integrated microfluidic (MF) device. (E) Maximal thrombus area (μm 2 ) occupied by calcein-labeled platelets from healthy donors vs patients (n = 10 mice per group, 10 individuals for each of the 2 groups, 3 arteriole injuries per mouse). The central box represents the values between the 10th and 90th percentiles, and the middle line is the mean. Statistical significance was determined using Mann-Whitney U test. ∗∗∗ P < 0.001 relative to healthy donors; ∗∗∗ P < 0.001 ADP relative to TRAP-6 for patients on DAPT.

    Article Snippet: The thrombin inhibitor H-D-Phe-Pro-Arg-chloromethylketone (PPACK), Alexa Fluor 488–conjugated mouse anti-human CD61, and Alexa Fluor 647–conjugated human fibrinogen were obtained from Bio-Rad and Thermo Fisher Scientific, respectively.

    Techniques: In Vitro, Fluorescence, Coagulation, Microscopy, Labeling, MANN-WHITNEY