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human notch3 elisa kit  (Cusabio)


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    Structured Review

    Cusabio human notch3 elisa kit
    Biomarker discovery by quantitative proteomics. ( A ) Plasma microvesicle isolation was carried out based on the vascular event outcomes of ischemic stroke patients, following a specific workflow. ( B ) A heatmap was generated to display the differentially upregulated proteins in the Event+ and Event− groups, respectively, where P < 0.05. ( C ) The differentially expressed proteins underwent pathway analysis using the PANTHER Classification System. ( D ) The Genotype-Tissue Expression (GTEx) portal revealed that <t>Notch3</t> is predominantly expressed in arterial tissues.
    Human Notch3 Elisa Kit, supplied by Cusabio, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+notch3+elisa+kit/Human+Neurogenic+locus+notch+homolog+protein+3(NOTCH3)+ELISA+kit/pmc11760494-165-13-17
    Average 92 stars, based on 2 article reviews
    human notch3 elisa kit - by Bioz Stars, 2026-09
    92/100 stars

    Images

    1) Product Images from "Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke"

    Article Title: Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke

    Journal: QJM: An International Journal of Medicine

    doi: 10.1093/qjmed/hcae136

    Biomarker discovery by quantitative proteomics. ( A ) Plasma microvesicle isolation was carried out based on the vascular event outcomes of ischemic stroke patients, following a specific workflow. ( B ) A heatmap was generated to display the differentially upregulated proteins in the Event+ and Event− groups, respectively, where P < 0.05. ( C ) The differentially expressed proteins underwent pathway analysis using the PANTHER Classification System. ( D ) The Genotype-Tissue Expression (GTEx) portal revealed that Notch3 is predominantly expressed in arterial tissues.
    Figure Legend Snippet: Biomarker discovery by quantitative proteomics. ( A ) Plasma microvesicle isolation was carried out based on the vascular event outcomes of ischemic stroke patients, following a specific workflow. ( B ) A heatmap was generated to display the differentially upregulated proteins in the Event+ and Event− groups, respectively, where P < 0.05. ( C ) The differentially expressed proteins underwent pathway analysis using the PANTHER Classification System. ( D ) The Genotype-Tissue Expression (GTEx) portal revealed that Notch3 is predominantly expressed in arterial tissues.

    Techniques Used: Biomarker Assay, Isolation, Generated, Expressing

    Plasma NOTCH3 predicts cardiovascular recurrence in men with ischemic stroke. NOTCH3 protein levels were measured directly in plasma samples of ( A ) the discovery cohort comparing levels among ischemic stroke patients with and without events (Event+ and Event−, respectively), and in ( B ) a larger validation cohort comparing plasma NOTCH3 in ischemic stroke patients with and without events (Event+ and Event−, respectively) and age-matched healthy controls. ( C ) The Kaplan–Meier plot shows survival probability of men with ischemic stroke according to quartiles of plasma NOTCH3 (log-rank P values = 0.020) suggesting that individuals in the highest quartile (>1600 pg/ml) of plasma NOTCH3 are more likely to experience cardiovascular recurrence. Statistical analysis was performed using Student’s t -test with Bonferroni adjustments, where * P < 0.05, ** P < 0.01 and *** P < 0.001.
    Figure Legend Snippet: Plasma NOTCH3 predicts cardiovascular recurrence in men with ischemic stroke. NOTCH3 protein levels were measured directly in plasma samples of ( A ) the discovery cohort comparing levels among ischemic stroke patients with and without events (Event+ and Event−, respectively), and in ( B ) a larger validation cohort comparing plasma NOTCH3 in ischemic stroke patients with and without events (Event+ and Event−, respectively) and age-matched healthy controls. ( C ) The Kaplan–Meier plot shows survival probability of men with ischemic stroke according to quartiles of plasma NOTCH3 (log-rank P values = 0.020) suggesting that individuals in the highest quartile (>1600 pg/ml) of plasma NOTCH3 are more likely to experience cardiovascular recurrence. Statistical analysis was performed using Student’s t -test with Bonferroni adjustments, where * P < 0.05, ** P < 0.01 and *** P < 0.001.

    Techniques Used:

    Comparison in demographic, stroke characteristics, risk factors, laboratory investigations and cardiovascular events in men and women <xref ref-type= a " title="Comparison in demographic, stroke characteristics, risk factors, laboratory investigations and cardiovascular events in ... " property="contentUrl" width="100%" height="100%"/>
    Figure Legend Snippet: Comparison in demographic, stroke characteristics, risk factors, laboratory investigations and cardiovascular events in men and women a

    Techniques Used: Comparison, Cell Counting, Biomarker Assay

    The hazard ratio (HR) and 95% confidence intervals (CI) of cardiovascular recurrence were analyzed based on plasma  NOTCH3  quartiles a
    Figure Legend Snippet: The hazard ratio (HR) and 95% confidence intervals (CI) of cardiovascular recurrence were analyzed based on plasma NOTCH3 quartiles a

    Techniques Used:

    NOTCH3 expression shows increased levels in mouse models of stroke and atherosclerosis. ( A ) Serial densitometric analysis and quantification of NOTCH3 protein in mouse serum following middle cerebral artery occlusion revealed a peak in NOTCH3 levels at 24 h, which continued to persist up to 72 h after cerebral reperfusion. Two technical replicates and pooled serum from six mice. ( B ) Representative immunofluorescence images of the innominate arteries of 22-week-old wild-type mice and Apoe-/- mice with advanced atherosclerotic plaque were examined. The images show NOTCH3-expressing endothelial cells in association with the plaque region. White arrowheads were used to indicate the location of these NOTCH3-expressing endothelial cells ( n = 3; L, lumen; P, plaque region). The scale bar represents 20 µm. ( C ) A quantification was performed to assess the number of NOTCH3-expressing endothelial cells in 14–20 analyzed arterial sections across three wild-type mice compared to three Apoe-/- mice. Data represent mean ± standard deviation; one-way ANOVA analysis; ** P < 0.01; *** P < 0.001; ns, non-significant.
    Figure Legend Snippet: NOTCH3 expression shows increased levels in mouse models of stroke and atherosclerosis. ( A ) Serial densitometric analysis and quantification of NOTCH3 protein in mouse serum following middle cerebral artery occlusion revealed a peak in NOTCH3 levels at 24 h, which continued to persist up to 72 h after cerebral reperfusion. Two technical replicates and pooled serum from six mice. ( B ) Representative immunofluorescence images of the innominate arteries of 22-week-old wild-type mice and Apoe-/- mice with advanced atherosclerotic plaque were examined. The images show NOTCH3-expressing endothelial cells in association with the plaque region. White arrowheads were used to indicate the location of these NOTCH3-expressing endothelial cells ( n = 3; L, lumen; P, plaque region). The scale bar represents 20 µm. ( C ) A quantification was performed to assess the number of NOTCH3-expressing endothelial cells in 14–20 analyzed arterial sections across three wild-type mice compared to three Apoe-/- mice. Data represent mean ± standard deviation; one-way ANOVA analysis; ** P < 0.01; *** P < 0.001; ns, non-significant.

    Techniques Used: Expressing, Immunofluorescence, Standard Deviation

    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke
    Article Snippet: .. We first sought to validate our previous findings using a commercial ELISA assay (Human NOTCH3 ELISA kit, Cusabio) on plasma samples from the same group of patients. ..

    Clinical Proteomics:

    Article Title: Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke
    Article Snippet: .. We first sought to validate our previous findings using a commercial ELISA assay (Human NOTCH3 ELISA kit, Cusabio) on plasma samples from the same group of patients. ..



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    Cusabio human notch3 elisa kit
    Biomarker discovery by quantitative proteomics. ( A ) Plasma microvesicle isolation was carried out based on the vascular event outcomes of ischemic stroke patients, following a specific workflow. ( B ) A heatmap was generated to display the differentially upregulated proteins in the Event+ and Event− groups, respectively, where P < 0.05. ( C ) The differentially expressed proteins underwent pathway analysis using the PANTHER Classification System. ( D ) The Genotype-Tissue Expression (GTEx) portal revealed that <t>Notch3</t> is predominantly expressed in arterial tissues.
    Human Notch3 Elisa Kit, supplied by Cusabio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+notch3+elisa+kit/Human+Neurogenic+locus+notch+homolog+protein+3(NOTCH3)+ELISA+kit/pmc11760494-165-13-17
    Average 92 stars, based on 1 article reviews
    human notch3 elisa kit - by Bioz Stars, 2026-09
    92/100 stars
      Buy from Supplier

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    Biomarker discovery by quantitative proteomics. ( A ) Plasma microvesicle isolation was carried out based on the vascular event outcomes of ischemic stroke patients, following a specific workflow. ( B ) A heatmap was generated to display the differentially upregulated proteins in the Event+ and Event− groups, respectively, where P < 0.05. ( C ) The differentially expressed proteins underwent pathway analysis using the PANTHER Classification System. ( D ) The Genotype-Tissue Expression (GTEx) portal revealed that Notch3 is predominantly expressed in arterial tissues.

    Journal: QJM: An International Journal of Medicine

    Article Title: Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke

    doi: 10.1093/qjmed/hcae136

    Figure Lengend Snippet: Biomarker discovery by quantitative proteomics. ( A ) Plasma microvesicle isolation was carried out based on the vascular event outcomes of ischemic stroke patients, following a specific workflow. ( B ) A heatmap was generated to display the differentially upregulated proteins in the Event+ and Event− groups, respectively, where P < 0.05. ( C ) The differentially expressed proteins underwent pathway analysis using the PANTHER Classification System. ( D ) The Genotype-Tissue Expression (GTEx) portal revealed that Notch3 is predominantly expressed in arterial tissues.

    Article Snippet: We first sought to validate our previous findings using a commercial ELISA assay (Human NOTCH3 ELISA kit, Cusabio) on plasma samples from the same group of patients.

    Techniques: Biomarker Assay, Isolation, Generated, Expressing

    Plasma NOTCH3 predicts cardiovascular recurrence in men with ischemic stroke. NOTCH3 protein levels were measured directly in plasma samples of ( A ) the discovery cohort comparing levels among ischemic stroke patients with and without events (Event+ and Event−, respectively), and in ( B ) a larger validation cohort comparing plasma NOTCH3 in ischemic stroke patients with and without events (Event+ and Event−, respectively) and age-matched healthy controls. ( C ) The Kaplan–Meier plot shows survival probability of men with ischemic stroke according to quartiles of plasma NOTCH3 (log-rank P values = 0.020) suggesting that individuals in the highest quartile (>1600 pg/ml) of plasma NOTCH3 are more likely to experience cardiovascular recurrence. Statistical analysis was performed using Student’s t -test with Bonferroni adjustments, where * P < 0.05, ** P < 0.01 and *** P < 0.001.

    Journal: QJM: An International Journal of Medicine

    Article Title: Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke

    doi: 10.1093/qjmed/hcae136

    Figure Lengend Snippet: Plasma NOTCH3 predicts cardiovascular recurrence in men with ischemic stroke. NOTCH3 protein levels were measured directly in plasma samples of ( A ) the discovery cohort comparing levels among ischemic stroke patients with and without events (Event+ and Event−, respectively), and in ( B ) a larger validation cohort comparing plasma NOTCH3 in ischemic stroke patients with and without events (Event+ and Event−, respectively) and age-matched healthy controls. ( C ) The Kaplan–Meier plot shows survival probability of men with ischemic stroke according to quartiles of plasma NOTCH3 (log-rank P values = 0.020) suggesting that individuals in the highest quartile (>1600 pg/ml) of plasma NOTCH3 are more likely to experience cardiovascular recurrence. Statistical analysis was performed using Student’s t -test with Bonferroni adjustments, where * P < 0.05, ** P < 0.01 and *** P < 0.001.

    Article Snippet: We first sought to validate our previous findings using a commercial ELISA assay (Human NOTCH3 ELISA kit, Cusabio) on plasma samples from the same group of patients.

    Techniques:

    Comparison in demographic, stroke characteristics, risk factors, laboratory investigations and cardiovascular events in men and women <xref ref-type= a " width="100%" height="100%">

    Journal: QJM: An International Journal of Medicine

    Article Title: Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke

    doi: 10.1093/qjmed/hcae136

    Figure Lengend Snippet: Comparison in demographic, stroke characteristics, risk factors, laboratory investigations and cardiovascular events in men and women a

    Article Snippet: We first sought to validate our previous findings using a commercial ELISA assay (Human NOTCH3 ELISA kit, Cusabio) on plasma samples from the same group of patients.

    Techniques: Comparison, Cell Counting, Biomarker Assay

    The hazard ratio (HR) and 95% confidence intervals (CI) of cardiovascular recurrence were analyzed based on plasma  NOTCH3  quartiles a

    Journal: QJM: An International Journal of Medicine

    Article Title: Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke

    doi: 10.1093/qjmed/hcae136

    Figure Lengend Snippet: The hazard ratio (HR) and 95% confidence intervals (CI) of cardiovascular recurrence were analyzed based on plasma NOTCH3 quartiles a

    Article Snippet: We first sought to validate our previous findings using a commercial ELISA assay (Human NOTCH3 ELISA kit, Cusabio) on plasma samples from the same group of patients.

    Techniques:

    NOTCH3 expression shows increased levels in mouse models of stroke and atherosclerosis. ( A ) Serial densitometric analysis and quantification of NOTCH3 protein in mouse serum following middle cerebral artery occlusion revealed a peak in NOTCH3 levels at 24 h, which continued to persist up to 72 h after cerebral reperfusion. Two technical replicates and pooled serum from six mice. ( B ) Representative immunofluorescence images of the innominate arteries of 22-week-old wild-type mice and Apoe-/- mice with advanced atherosclerotic plaque were examined. The images show NOTCH3-expressing endothelial cells in association with the plaque region. White arrowheads were used to indicate the location of these NOTCH3-expressing endothelial cells ( n = 3; L, lumen; P, plaque region). The scale bar represents 20 µm. ( C ) A quantification was performed to assess the number of NOTCH3-expressing endothelial cells in 14–20 analyzed arterial sections across three wild-type mice compared to three Apoe-/- mice. Data represent mean ± standard deviation; one-way ANOVA analysis; ** P < 0.01; *** P < 0.001; ns, non-significant.

    Journal: QJM: An International Journal of Medicine

    Article Title: Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke

    doi: 10.1093/qjmed/hcae136

    Figure Lengend Snippet: NOTCH3 expression shows increased levels in mouse models of stroke and atherosclerosis. ( A ) Serial densitometric analysis and quantification of NOTCH3 protein in mouse serum following middle cerebral artery occlusion revealed a peak in NOTCH3 levels at 24 h, which continued to persist up to 72 h after cerebral reperfusion. Two technical replicates and pooled serum from six mice. ( B ) Representative immunofluorescence images of the innominate arteries of 22-week-old wild-type mice and Apoe-/- mice with advanced atherosclerotic plaque were examined. The images show NOTCH3-expressing endothelial cells in association with the plaque region. White arrowheads were used to indicate the location of these NOTCH3-expressing endothelial cells ( n = 3; L, lumen; P, plaque region). The scale bar represents 20 µm. ( C ) A quantification was performed to assess the number of NOTCH3-expressing endothelial cells in 14–20 analyzed arterial sections across three wild-type mice compared to three Apoe-/- mice. Data represent mean ± standard deviation; one-way ANOVA analysis; ** P < 0.01; *** P < 0.001; ns, non-significant.

    Article Snippet: We first sought to validate our previous findings using a commercial ELISA assay (Human NOTCH3 ELISA kit, Cusabio) on plasma samples from the same group of patients.

    Techniques: Expressing, Immunofluorescence, Standard Deviation