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human saa1 elisa kit  (R&D Systems)


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    Structured Review

    R&D Systems human saa1 elisa kit
    Enhanced <t>SAA1</t> expression and NET formation in plasma of MS patients. (A) SAA1 protein expression was quantified by ELISA in plasma samples collected from MS patients and HC. (B) H3.1-nucleosome expression was quantified by ELISA in plasma samples collected from MS patients and HC
    Human Saa1 Elisa Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 45 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/saa1+duoset+elisa+kit/Human+Serum+Amyloid+A1+DuoSet+ELISA/pmc13112694-72-1-6
    Average 93 stars, based on 45 article reviews
    human saa1 elisa kit - by Bioz Stars, 2026-10
    93/100 stars

    Images

    1) Product Images from "Single-cell RNA sequencing uncovers neutrophil clusters associated with autoimmune neuroinflammation"

    Article Title: Single-cell RNA sequencing uncovers neutrophil clusters associated with autoimmune neuroinflammation

    Journal: Journal of Neuroinflammation

    doi: 10.1186/s12974-026-03772-9

    Enhanced SAA1 expression and NET formation in plasma of MS patients. (A) SAA1 protein expression was quantified by ELISA in plasma samples collected from MS patients and HC. (B) H3.1-nucleosome expression was quantified by ELISA in plasma samples collected from MS patients and HC
    Figure Legend Snippet: Enhanced SAA1 expression and NET formation in plasma of MS patients. (A) SAA1 protein expression was quantified by ELISA in plasma samples collected from MS patients and HC. (B) H3.1-nucleosome expression was quantified by ELISA in plasma samples collected from MS patients and HC

    Techniques Used: Expressing, Clinical Proteomics, Enzyme-linked Immunosorbent Assay

    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Elevated Serum Amyloid A Levels Contribute to Increased Platelet Adhesion in COVID-19 Patients.
    Article Snippet: .. An SAA-specific ELISA (SAA1 DuoSet ELISA Kit, R&D Systems, MN USA) was used to detect and quantify the SAA levels in the platelets of healthy and COVID-19 patients according to the manufacturer’s instructions. ..

    Article Title: Elevated Serum Amyloid A Levels Contribute to Increased Platelet Adhesion in COVID-19 Patients
    Article Snippet: .. An SAA-specific ELISA (SAA1 DuoSet ELISA Kit, R&D Systems, MN USA) was used to detect and quantify the SAA levels in the platelets of healthy and COVID-19 patients according to the manufacturer’s instructions. ..



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    Enhanced <t>SAA1</t> expression and NET formation in plasma of MS patients. (A) SAA1 protein expression was quantified by ELISA in plasma samples collected from MS patients and HC. (B) H3.1-nucleosome expression was quantified by ELISA in plasma samples collected from MS patients and HC
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    Enhanced <t>SAA1</t> expression and NET formation in plasma of MS patients. (A) SAA1 protein expression was quantified by ELISA in plasma samples collected from MS patients and HC. (B) H3.1-nucleosome expression was quantified by ELISA in plasma samples collected from MS patients and HC
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    R&D Systems human saa1 duoset elisa kit dy3019 05
    Enhanced <t>SAA1</t> expression and NET formation in plasma of MS patients. (A) SAA1 protein expression was quantified by ELISA in plasma samples collected from MS patients and HC. (B) H3.1-nucleosome expression was quantified by ELISA in plasma samples collected from MS patients and HC
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    R&D Systems saa1 duoset elisa kit
    Figure 1. SAA is bound to platelets from COVID-19 patients. (A) Mass spectrometry was used to identify and quantify proteins overexpressed in purified COVID-19 platelets compared to controls. Shown are proteins whose levels were consistently elevated in two independent experiments. Values indicate the average fold-change (FC) in the relative label-free quantification intensity between the COVID-19 and the control samples (n = 4 in each group). Unpaired Student’s t-test was used to determine the significance. (B) Platelet lysates from control or COVID-19 donors were separated using SDS-PAGE. SAA was detected using a specific antibody. Tubulin was used as a loading control. Results are representative of six controls and six COVID-19 patients. Numbers represent fold intensity of control densitometric values normalized to tubulin. (C) SAA levels in platelet lysates from controls (n = 17) or COVID-19 patients (n = 15) were determined using <t>ELISA.</t> The dashed line in the violin plot is the median. The dotted lines show the interquartile range. Unpaired t-test, **** p < 0.001. (D) Platelet lysates from control or COVID-19 donors separated according to disease severity were analyzed using SDS-PAGE (n = 6 controls, 9 mild, 5 moderate, and 20 severe disease patients). SAA was detected using a specific antibody. The results were normalized to tubulin and to the amount of total protein. Ordinary one-way ANOVA, Dunnett’s multiple comparisons compared to control, ns = non-significant, * p < 0.05.
    Saa1 Duoset Elisa Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    R&D Systems human saa1 duoset elisa development kit
    Figure 1. SAA is bound to platelets from COVID-19 patients. (A) Mass spectrometry was used to identify and quantify proteins overexpressed in purified COVID-19 platelets compared to controls. Shown are proteins whose levels were consistently elevated in two independent experiments. Values indicate the average fold-change (FC) in the relative label-free quantification intensity between the COVID-19 and the control samples (n = 4 in each group). Unpaired Student’s t-test was used to determine the significance. (B) Platelet lysates from control or COVID-19 donors were separated using SDS-PAGE. SAA was detected using a specific antibody. Tubulin was used as a loading control. Results are representative of six controls and six COVID-19 patients. Numbers represent fold intensity of control densitometric values normalized to tubulin. (C) SAA levels in platelet lysates from controls (n = 17) or COVID-19 patients (n = 15) were determined using <t>ELISA.</t> The dashed line in the violin plot is the median. The dotted lines show the interquartile range. Unpaired t-test, **** p < 0.001. (D) Platelet lysates from control or COVID-19 donors separated according to disease severity were analyzed using SDS-PAGE (n = 6 controls, 9 mild, 5 moderate, and 20 severe disease patients). SAA was detected using a specific antibody. The results were normalized to tubulin and to the amount of total protein. Ordinary one-way ANOVA, Dunnett’s multiple comparisons compared to control, ns = non-significant, * p < 0.05.
    Human Saa1 Duoset Elisa Development Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 94 stars, based on 1 article reviews
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    Image Search Results


    Enhanced SAA1 expression and NET formation in plasma of MS patients. (A) SAA1 protein expression was quantified by ELISA in plasma samples collected from MS patients and HC. (B) H3.1-nucleosome expression was quantified by ELISA in plasma samples collected from MS patients and HC

    Journal: Journal of Neuroinflammation

    Article Title: Single-cell RNA sequencing uncovers neutrophil clusters associated with autoimmune neuroinflammation

    doi: 10.1186/s12974-026-03772-9

    Figure Lengend Snippet: Enhanced SAA1 expression and NET formation in plasma of MS patients. (A) SAA1 protein expression was quantified by ELISA in plasma samples collected from MS patients and HC. (B) H3.1-nucleosome expression was quantified by ELISA in plasma samples collected from MS patients and HC

    Article Snippet: The human SAA1 ELISA kit (DY3019-05; R & D Systems, Minneapolis, MN) detected human SAA1 in plasma samples from MS patients and HC.

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

    Figure 1. SAA is bound to platelets from COVID-19 patients. (A) Mass spectrometry was used to identify and quantify proteins overexpressed in purified COVID-19 platelets compared to controls. Shown are proteins whose levels were consistently elevated in two independent experiments. Values indicate the average fold-change (FC) in the relative label-free quantification intensity between the COVID-19 and the control samples (n = 4 in each group). Unpaired Student’s t-test was used to determine the significance. (B) Platelet lysates from control or COVID-19 donors were separated using SDS-PAGE. SAA was detected using a specific antibody. Tubulin was used as a loading control. Results are representative of six controls and six COVID-19 patients. Numbers represent fold intensity of control densitometric values normalized to tubulin. (C) SAA levels in platelet lysates from controls (n = 17) or COVID-19 patients (n = 15) were determined using ELISA. The dashed line in the violin plot is the median. The dotted lines show the interquartile range. Unpaired t-test, **** p < 0.001. (D) Platelet lysates from control or COVID-19 donors separated according to disease severity were analyzed using SDS-PAGE (n = 6 controls, 9 mild, 5 moderate, and 20 severe disease patients). SAA was detected using a specific antibody. The results were normalized to tubulin and to the amount of total protein. Ordinary one-way ANOVA, Dunnett’s multiple comparisons compared to control, ns = non-significant, * p < 0.05.

    Journal: International journal of molecular sciences

    Article Title: Elevated Serum Amyloid A Levels Contribute to Increased Platelet Adhesion in COVID-19 Patients.

    doi: 10.3390/ijms232214243

    Figure Lengend Snippet: Figure 1. SAA is bound to platelets from COVID-19 patients. (A) Mass spectrometry was used to identify and quantify proteins overexpressed in purified COVID-19 platelets compared to controls. Shown are proteins whose levels were consistently elevated in two independent experiments. Values indicate the average fold-change (FC) in the relative label-free quantification intensity between the COVID-19 and the control samples (n = 4 in each group). Unpaired Student’s t-test was used to determine the significance. (B) Platelet lysates from control or COVID-19 donors were separated using SDS-PAGE. SAA was detected using a specific antibody. Tubulin was used as a loading control. Results are representative of six controls and six COVID-19 patients. Numbers represent fold intensity of control densitometric values normalized to tubulin. (C) SAA levels in platelet lysates from controls (n = 17) or COVID-19 patients (n = 15) were determined using ELISA. The dashed line in the violin plot is the median. The dotted lines show the interquartile range. Unpaired t-test, **** p < 0.001. (D) Platelet lysates from control or COVID-19 donors separated according to disease severity were analyzed using SDS-PAGE (n = 6 controls, 9 mild, 5 moderate, and 20 severe disease patients). SAA was detected using a specific antibody. The results were normalized to tubulin and to the amount of total protein. Ordinary one-way ANOVA, Dunnett’s multiple comparisons compared to control, ns = non-significant, * p < 0.05.

    Article Snippet: An SAA-specific ELISA (SAA1 DuoSet ELISA Kit, R&D Systems, MN USA) was used to detect and quantify the SAA levels in the platelets of healthy and COVID-19 patients according to the manufacturer’s instructions.

    Techniques: Mass Spectrometry, Control, SDS Page, Enzyme-linked Immunosorbent Assay