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elisa serum amyloid a saa  (BioVendor Instruments)


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    BioVendor Instruments elisa serum amyloid a saa
    Elisa Serum Amyloid A Saa, supplied by BioVendor Instruments, used in various techniques. Bioz Stars score: 93/100, based on 147 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/elisa+serum+amyloid+a+saa/Leptin+Mouse%2FRat+ELISA/pmc12655664-186-9-16
    Average 93 stars, based on 147 article reviews
    elisa serum amyloid a saa - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: VDAC1 Intervention Alleviates Bisphenol AF-Induced Succinate Metabolism Dysregulation and Inflammatory Responses
    Article Snippet: .. Inflammatory cytokine levels in the serum were measured using ELISA: serum amyloid A (SAA) (Mouse SAA, BioVendor #RD291001200R, Asheville, NC, USA), TNF-α, IL-1β, IL-6 (the same Beyotime ELISA kit, Shanghai, China). ..



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    (A ) Paraoxonase-1 (PON-1) activity of HDL, ( B ) serum amyloid A1 <t>(SAA-1)</t> content of HDL and ( C ) the ratio of PON-1 to SAA-1 on HDL in Europeans (EUs, n =21) and South Asians (SAs, n =14) before and after weight gain. Data expressed as median ± interquartile range and shown on a log10 axis for clear visualisation. ( D ) % inhibition of TNFα-induced VCAM-1 expression by HDL in endothelial cells in EUs ( n =21) and SAs ( n =14) before and after weight gain. Data expressed as mean ± standard deviation. Comparisons were made in A-D by the mixed effects model. Statistical significance was assumed at P <0.05.
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    (A ) Paraoxonase-1 (PON-1) activity of HDL, ( B ) serum amyloid A1 <t>(SAA-1)</t> content of HDL and ( C ) the ratio of PON-1 to SAA-1 on HDL in Europeans (EUs, n =21) and South Asians (SAs, n =14) before and after weight gain. Data expressed as median ± interquartile range and shown on a log10 axis for clear visualisation. ( D ) % inhibition of TNFα-induced VCAM-1 expression by HDL in endothelial cells in EUs ( n =21) and SAs ( n =14) before and after weight gain. Data expressed as mean ± standard deviation. Comparisons were made in A-D by the mixed effects model. Statistical significance was assumed at P <0.05.
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    Image Search Results


    Verification of potential biomarkers for AS. (A) Expression levels of SAA1, FERMT3, ILK, and TLN1 in plasma samples from active-stage AS patients, stable-stage AS patients, and healthy controls measured by proteomics. ROC curves for the individual protein (SAA1, FERMT3, ILK, and TLN1) as a predictor to classify AS patients from healthy controls (B), and active-stage AS patients from stable-stage AS patients (C). (D) ELISA analysis of SAA1, FERMT3, ILK, and TLN1 expressions in the plasma samples from an independent validation cohort of healthy controls (N, n = 24), active-stage AS (A, n = 27), and stable-stage AS patients (S, n = 28). Statistical analyses employed Wilcoxon rank-sum test for intergroup comparisons, with results reported as mean ± SEM. Significance thresholds based on BH-adjusted p -values were defined as: *, <0.05; **, <0.01; ***, <0.001.

    Journal: Journal of Advanced Research

    Article Title: Characterization of immune features and discovery of potential biomarkers for ankylosing spondylitis using deep plasma proteomics

    doi: 10.1016/j.jare.2025.05.052

    Figure Lengend Snippet: Verification of potential biomarkers for AS. (A) Expression levels of SAA1, FERMT3, ILK, and TLN1 in plasma samples from active-stage AS patients, stable-stage AS patients, and healthy controls measured by proteomics. ROC curves for the individual protein (SAA1, FERMT3, ILK, and TLN1) as a predictor to classify AS patients from healthy controls (B), and active-stage AS patients from stable-stage AS patients (C). (D) ELISA analysis of SAA1, FERMT3, ILK, and TLN1 expressions in the plasma samples from an independent validation cohort of healthy controls (N, n = 24), active-stage AS (A, n = 27), and stable-stage AS patients (S, n = 28). Statistical analyses employed Wilcoxon rank-sum test for intergroup comparisons, with results reported as mean ± SEM. Significance thresholds based on BH-adjusted p -values were defined as: *, <0.05; **, <0.01; ***, <0.001.

    Article Snippet: The human serum amyloid A (SAA1) ELISA kit (#OKIA00083) was purchased from Aviva Systems Biology Company (San Diego, CA, USA).

    Techniques: Expressing, Clinical Proteomics, Enzyme-linked Immunosorbent Assay, Biomarker Discovery

    (A ) Paraoxonase-1 (PON-1) activity of HDL, ( B ) serum amyloid A1 (SAA-1) content of HDL and ( C ) the ratio of PON-1 to SAA-1 on HDL in Europeans (EUs, n =21) and South Asians (SAs, n =14) before and after weight gain. Data expressed as median ± interquartile range and shown on a log10 axis for clear visualisation. ( D ) % inhibition of TNFα-induced VCAM-1 expression by HDL in endothelial cells in EUs ( n =21) and SAs ( n =14) before and after weight gain. Data expressed as mean ± standard deviation. Comparisons were made in A-D by the mixed effects model. Statistical significance was assumed at P <0.05.

    Journal: Clinical Science (London, England : 1979)

    Article Title: HDL protein composition differs between young white European and South Asian men before and after weight gain

    doi: 10.1042/CS20258040

    Figure Lengend Snippet: (A ) Paraoxonase-1 (PON-1) activity of HDL, ( B ) serum amyloid A1 (SAA-1) content of HDL and ( C ) the ratio of PON-1 to SAA-1 on HDL in Europeans (EUs, n =21) and South Asians (SAs, n =14) before and after weight gain. Data expressed as median ± interquartile range and shown on a log10 axis for clear visualisation. ( D ) % inhibition of TNFα-induced VCAM-1 expression by HDL in endothelial cells in EUs ( n =21) and SAs ( n =14) before and after weight gain. Data expressed as mean ± standard deviation. Comparisons were made in A-D by the mixed effects model. Statistical significance was assumed at P <0.05.

    Article Snippet: HDL apoA-I and serum amyloid A1 (SAA-1) were measured by R&D Systems DuoSet ELISA (#DY3664 and #DY3019) according to the manufacturer’s protocol.

    Techniques: Activity Assay, Inhibition, Expressing, Standard Deviation