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cst3 cystatin c elisa kit  (Sino Biological)


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    Sino Biological cst3 cystatin c elisa kit
    Cst3 Cystatin C Elisa Kit, supplied by Sino Biological, used in various techniques. Bioz Stars score: 94/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/elisa+pair+set/Human+Cystatin+C+%2F+CST3+ELISA+Pair+Set/pm41998026-79-0-8
    Average 94 stars, based on 5 article reviews
    cst3 cystatin c elisa kit - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Urine biomarkers enable pancreatic cancer detection up to 2 years before diagnosis.
    Article Snippet: .. REG1B was assayed with the ELISA Pair Set, Sino Biological Inc. (Cat# SEK11638; 1:500 urine dilutions) with TMB Substrate reagent and Stop Solution from BioLegend (Cat# 421101 and 423 001). ..

    Article Title: Environmental Exposure to Cadmium and Lead Exacerbates Kidney Function in People with Diabetes
    Article Snippet: .. Urinary and serum concentrations of β 2 M were determined using the human beta-2 microglobulin/β 2 M ELISA pair set (Sino Biological Inc., Wayne, PA, USA). ..

    Article Title: Recent advances in the potential applications of luminescence-based, SPR-based, and carbon-based biosensors
    Article Snippet: Fluorescent aptasensor , H5N1 influenza A (rHA protein) , 2 ng/mL (in aqueous buffer); 3.5 ng/mL (in human serum) , Influenza A H5N1 (avian flu) hemagglutinin/HA ELISA Pair Set; antibodies-online GmbH (LOD = 78.125 pg/mL) , Self-contained diagnostic kit, detection can be performed in polyethylene tube within 30 min , Pang et al. ( ) . .. Electrochemical immunosensor , Zika virus (envelope protein) , 10 pM , Zika virus (strain Zika SPH2015) envelope protein (ZIKV-E) ELISA Pair Set; Sino Biological Inc. (LOD = 125 pg/mL) , Promising clinical application for early-stage diagnostics of the virus, operation time around 40 min , Kaushik et al. ( ) . ..

    Article Title: Evidence Linking Cadmium Exposure and β 2 -Microglobulin to Increased Risk of Hypertension in Diabetes Type 2
    Article Snippet: .. The human beta-2 microglobulin/β 2 M ELISA pair set (Sino Biological Inc., Wayne, PA, USA) was employed to determine serum and urine concentration of β 2 M ([β 2 M] s and [β 2 M] u ) with the low detection limit of 3.13 pg/mL. .. Blood Cd concentration ([Cd] b ) was determined with the atomic absorption spectrophotometer (GBC Scientific Equipment, Hampshire, IL, USA).

    Article Title: Exogenous analogues of substance P trigger pseudo-allergic reactions through activation of MRGPRX2
    Article Snippet: Pseudo-allergic reactions are non-IgE-mediated immediate allergic reactions, and MRGPRX2 is a potential important target for pseudo-allergic reactions.. Currently, numerous reports focus on the induction of pseudo-allergic reactions by small molecule drugs and endogenous peptides.. However, insufficient attention has been paid to the pseudo-allergic reactions induced by exogenous peptides through MRGPRX2.

    Article Title: Amyloid-like fibrils derived from β -sheets of gp120 contribute to the neuronal pathology of HIV-associated neurocognitive disorders
    Article Snippet: Visualization was carried out using a Fluor Chem E imaging system (ProteinSimple, San Jose, USA), followed by analysis using Image J. .. ELISA assays were conducted using the HIV-1 gp120 ELISA Pair Set (Sino Biological, Beijing, China, #SEK11233-5), Mouse Aβ1–42 ELISA Pair Set (LabRe, #LB2220B), Human βAmyloid1–42 ELISA Pair Set (Mreda, #MF00133). ..

    Article Title: Low levels of serum complement factor H is associated with increasing progression of bronchiectasis
    Article Snippet: Enzyme-Linked Immunorsorbent Assay (ELISA) A sandwich ELISA kit, specific for CFH was used to determine the levels of CFH in serum from both patients and control. .. A Sino Biological ELISA pair set (SEK 10714) was used for the purpose of this research; it is an expression of a solid phase sandwich ELISA. ..

    Article Title: Enhanced Kidney Damage in Individuals with Diabetes Who Are Chronically Exposed to Cadmium and Lead: The Emergent Role for β 2 -Microglobulin
    Article Snippet: .. We used the human beta-2 microglobulin/β 2 M ELISA pair set (Sino Biological Inc., Wayne, PA, USA) to determine urine and serum concentration of β 2 M, with a lower limit of detection of 3.13 pg/mL. .. The plasma glucose assay was based on the oxidase–peroxidase method (Glu Colorimetric Assay Kit, Elabscience, Catalog No: E-BC-K234-M, Houston, TX, USA) [ ].

    Virus:

    Article Title: Recent advances in the potential applications of luminescence-based, SPR-based, and carbon-based biosensors
    Article Snippet: Fluorescent aptasensor , H5N1 influenza A (rHA protein) , 2 ng/mL (in aqueous buffer); 3.5 ng/mL (in human serum) , Influenza A H5N1 (avian flu) hemagglutinin/HA ELISA Pair Set; antibodies-online GmbH (LOD = 78.125 pg/mL) , Self-contained diagnostic kit, detection can be performed in polyethylene tube within 30 min , Pang et al. ( ) . .. Electrochemical immunosensor , Zika virus (envelope protein) , 10 pM , Zika virus (strain Zika SPH2015) envelope protein (ZIKV-E) ELISA Pair Set; Sino Biological Inc. (LOD = 125 pg/mL) , Promising clinical application for early-stage diagnostics of the virus, operation time around 40 min , Kaushik et al. ( ) . ..

    Concentration Assay:

    Article Title: Evidence Linking Cadmium Exposure and β 2 -Microglobulin to Increased Risk of Hypertension in Diabetes Type 2
    Article Snippet: .. The human beta-2 microglobulin/β 2 M ELISA pair set (Sino Biological Inc., Wayne, PA, USA) was employed to determine serum and urine concentration of β 2 M ([β 2 M] s and [β 2 M] u ) with the low detection limit of 3.13 pg/mL. .. Blood Cd concentration ([Cd] b ) was determined with the atomic absorption spectrophotometer (GBC Scientific Equipment, Hampshire, IL, USA).

    Article Title: Enhanced Kidney Damage in Individuals with Diabetes Who Are Chronically Exposed to Cadmium and Lead: The Emergent Role for β 2 -Microglobulin
    Article Snippet: .. We used the human beta-2 microglobulin/β 2 M ELISA pair set (Sino Biological Inc., Wayne, PA, USA) to determine urine and serum concentration of β 2 M, with a lower limit of detection of 3.13 pg/mL. .. The plasma glucose assay was based on the oxidase–peroxidase method (Glu Colorimetric Assay Kit, Elabscience, Catalog No: E-BC-K234-M, Houston, TX, USA) [ ].

    Expressing:

    Article Title: Low levels of serum complement factor H is associated with increasing progression of bronchiectasis
    Article Snippet: Enzyme-Linked Immunorsorbent Assay (ELISA) A sandwich ELISA kit, specific for CFH was used to determine the levels of CFH in serum from both patients and control. .. A Sino Biological ELISA pair set (SEK 10714) was used for the purpose of this research; it is an expression of a solid phase sandwich ELISA. ..

    Sandwich ELISA:

    Article Title: Low levels of serum complement factor H is associated with increasing progression of bronchiectasis
    Article Snippet: Enzyme-Linked Immunorsorbent Assay (ELISA) A sandwich ELISA kit, specific for CFH was used to determine the levels of CFH in serum from both patients and control. .. A Sino Biological ELISA pair set (SEK 10714) was used for the purpose of this research; it is an expression of a solid phase sandwich ELISA. ..



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    ECC induced early systemic inflammatory responses and organ stress–associated biomarker changes. (A) Heatmap representation of plasma pro-inflammatory cytokine levels, including IL-1β, <t>IL-18,</t> IL-6, and TNF-α, measured in Control, Sham, and ECC groups at the end of the 60-min experimental period. Color intensity reflects relative concentration levels. Statistical comparisons among groups are indicated above the heatmap. (B) Heatmap comparison of plasma organ stress–associated biomarkers between Control and ECC groups at 60 min, including creatinine, cardiac troponin, AST/GOT, and LDH. Color intensity represents relative biomarker levels. P values for group comparisons are shown above each parameter. (C) Time-course analysis of myeloperoxidase (MPO) activity over a 30-min reaction period in plasma samples from Control, Sham, and ECC groups. MPO activity is expressed as optical density per minute (OD/min). ns, not significant.
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    Image Search Results


    Serum RNASE1 levels are elevated in patients with SLE and correlate with disease activity and renal dysfunction. (A) Serum RNASE1 concentrations measured by ELISA in healthy controls (HC) and patients with SLE. (B) Comparison of serum RNASE1 levels among HC, patients with SLE without nephritis, and patients with LN. (C) Serum RNASE1 levels in patients with SLE stratified according to disease activity based on SLEDAI scores (inactive, mild, moderate, and severe). (D, E) Correlation analyses between serum RNASE1 levels and SLEDAI scores (D) and complement C3 levels (E) in patients with SLE. (F–H) Correlation analyses between serum RNASE1 levels and renal function parameters in patients with LN, including urinary protein excretion (F) , serum creatinine (G) , and blood urea nitrogen (H) . (I) ROC curve evaluating the performance of serum RNASE1 levels in discriminating patients with SLE from healthy controls. (J–L) ROC curve analyses assessing the discriminative ability of serum RNASE1 levels for identifying patients with ≥mild disease activity (J) , ≥moderate disease activity (K) , and ≥severe disease activity (L) . * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001.

    Journal: Frontiers in Immunology

    Article Title: Serum RNASE1 as a biomarker for disease activity and lupus nephritis in systemic lupus erythematosus

    doi: 10.3389/fimmu.2026.1790455

    Figure Lengend Snippet: Serum RNASE1 levels are elevated in patients with SLE and correlate with disease activity and renal dysfunction. (A) Serum RNASE1 concentrations measured by ELISA in healthy controls (HC) and patients with SLE. (B) Comparison of serum RNASE1 levels among HC, patients with SLE without nephritis, and patients with LN. (C) Serum RNASE1 levels in patients with SLE stratified according to disease activity based on SLEDAI scores (inactive, mild, moderate, and severe). (D, E) Correlation analyses between serum RNASE1 levels and SLEDAI scores (D) and complement C3 levels (E) in patients with SLE. (F–H) Correlation analyses between serum RNASE1 levels and renal function parameters in patients with LN, including urinary protein excretion (F) , serum creatinine (G) , and blood urea nitrogen (H) . (I) ROC curve evaluating the performance of serum RNASE1 levels in discriminating patients with SLE from healthy controls. (J–L) ROC curve analyses assessing the discriminative ability of serum RNASE1 levels for identifying patients with ≥mild disease activity (J) , ≥moderate disease activity (K) , and ≥severe disease activity (L) . * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001.

    Article Snippet: Serum levels of RNASE1 were quantified using a commercially available ELISA kit (catalog no. SEK13468 ; Sino Biological Inc., Beijing, China) according to the manufacturer’s instructions.

    Techniques: Activity Assay, Enzyme-linked Immunosorbent Assay, Comparison

    ECC induced early systemic inflammatory responses and organ stress–associated biomarker changes. (A) Heatmap representation of plasma pro-inflammatory cytokine levels, including IL-1β, IL-18, IL-6, and TNF-α, measured in Control, Sham, and ECC groups at the end of the 60-min experimental period. Color intensity reflects relative concentration levels. Statistical comparisons among groups are indicated above the heatmap. (B) Heatmap comparison of plasma organ stress–associated biomarkers between Control and ECC groups at 60 min, including creatinine, cardiac troponin, AST/GOT, and LDH. Color intensity represents relative biomarker levels. P values for group comparisons are shown above each parameter. (C) Time-course analysis of myeloperoxidase (MPO) activity over a 30-min reaction period in plasma samples from Control, Sham, and ECC groups. MPO activity is expressed as optical density per minute (OD/min). ns, not significant.

    Journal: Frontiers in Physiology

    Article Title: A miniaturized mouse extracorporeal circulation model to characterize early hematologic and metabolic alterations

    doi: 10.3389/fphys.2026.1740282

    Figure Lengend Snippet: ECC induced early systemic inflammatory responses and organ stress–associated biomarker changes. (A) Heatmap representation of plasma pro-inflammatory cytokine levels, including IL-1β, IL-18, IL-6, and TNF-α, measured in Control, Sham, and ECC groups at the end of the 60-min experimental period. Color intensity reflects relative concentration levels. Statistical comparisons among groups are indicated above the heatmap. (B) Heatmap comparison of plasma organ stress–associated biomarkers between Control and ECC groups at 60 min, including creatinine, cardiac troponin, AST/GOT, and LDH. Color intensity represents relative biomarker levels. P values for group comparisons are shown above each parameter. (C) Time-course analysis of myeloperoxidase (MPO) activity over a 30-min reaction period in plasma samples from Control, Sham, and ECC groups. MPO activity is expressed as optical density per minute (OD/min). ns, not significant.

    Article Snippet: ELISA kits were obtained as follows: IL-1β (Cat. No. 88-7013a, Invitrogen, Thermo Fisher Scientific, United States), IL-6 (Cat. No. DY406, R&D Systems, United States), TNF-α (Cat. No. 88-7324, Invitrogen, Thermo Fisher Scientific, United States), and IL-18 (Cat. No. SEK50073 , Sino Biological Inc., China).

    Techniques: Biomarker Discovery, Clinical Proteomics, Control, Concentration Assay, Comparison, Activity Assay