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elisa  (BioVendor Instruments)


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    BioVendor Instruments elisa
    Elisa, 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/leptin+mouse+rat+elisa/Leptin+Mouse%2FRat+ELISA/pm41828836-305-33-37
    Average 93 stars, based on 147 article reviews
    elisa - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Effect of Maternal Obesity and Preconceptional Weight Loss on Male and Female Offspring Metabolism and Olfactory Performance in Mice
    Article Snippet: For F1, cholesterolemia was measured by enzymatic CHOD-PAP (cholesterol oxidase: p-aminophenazone) method (#WCHO100, Sobioda, Montbonnot-Saint-Martin, France). .. Leptinemia was measured with Leptin Mouse/Rat ELISA (#RD291001200R, BioVendor Laboratory Medicine, Brno, Czech Republic) according to the manufacturer’s guidelines. ..

    Article Title: Matcha Green Tea Improves Cafeteria-Diet-Induced NAFLD by Modulating the Gut Microbiota in Rats.
    Article Snippet: All cytokines were read at an absorbance of 450 nm with a microplate reader (Molecular Devices, Sunnyvale, CA, USA). .. Plasma leptin and adiponectin levels were determined with Leptin Mouse/Rat ELISA (Biovendor, Brno, Czech Republic) and Rat Adiponectin (Assay MaxTM, St. Charles, LA, USA) commercial ELISA kits. .. Both adipokines were read at an absorbance of 450 nm with a microplate reader (Molecular Devices).

    Article Title: Matcha Green Tea Improves Cafeteria-Diet-Induced NAFLD by Modulating the Gut Microbiota in Rats
    Article Snippet: All cytokines were read at an absorbance of 450 nm with a microplate reader (Molecular Devices, Sunnyvale, CA, USA). .. Plasma leptin and adiponectin levels were determined with Leptin Mouse/Rat ELISA (Biovendor, Brno, Czech Republic) and Rat Adiponectin (Assay MaxTM, St. Charles, LA, USA) commercial ELISA kits. .. Both adipokines were read at an absorbance of 450 nm with a microplate reader (Molecular Devices).

    Article Title: Antioxidants protect against diabetes by improving glucose homeostasis in mouse models of inducible insulin resistance and obesity
    Article Snippet: NEFA levels were measured using the NEFA-C kit (Wako Chemicals, Neuss, Germany). .. Leptin concentrations were measured with the leptin Mouse/Rat ELISA (BioVendor, RD291001200R, Heidelberg, Germany) and T 4 concentrations with the T 4 ELISA kit (Invitrogen, EIAT4C, Carlsbad, CA, USA). ..

    Clinical Proteomics:

    Article Title: Matcha Green Tea Improves Cafeteria-Diet-Induced NAFLD by Modulating the Gut Microbiota in Rats.
    Article Snippet: All cytokines were read at an absorbance of 450 nm with a microplate reader (Molecular Devices, Sunnyvale, CA, USA). .. Plasma leptin and adiponectin levels were determined with Leptin Mouse/Rat ELISA (Biovendor, Brno, Czech Republic) and Rat Adiponectin (Assay MaxTM, St. Charles, LA, USA) commercial ELISA kits. .. Both adipokines were read at an absorbance of 450 nm with a microplate reader (Molecular Devices).

    Article Title: Matcha Green Tea Improves Cafeteria-Diet-Induced NAFLD by Modulating the Gut Microbiota in Rats
    Article Snippet: All cytokines were read at an absorbance of 450 nm with a microplate reader (Molecular Devices, Sunnyvale, CA, USA). .. Plasma leptin and adiponectin levels were determined with Leptin Mouse/Rat ELISA (Biovendor, Brno, Czech Republic) and Rat Adiponectin (Assay MaxTM, St. Charles, LA, USA) commercial ELISA kits. .. Both adipokines were read at an absorbance of 450 nm with a microplate reader (Molecular Devices).



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    Obesity parameters and metabolic phenotype in male B6 mice. a Body weight (g) measurements over 12 weeks for LFD and HFD-fed male B6 mice ( n = 32-41). b Change in weight (%) (dotted line at 28% represents parameter for LFD and dotted line at 58% represents parameter for HFD). c Fold change in fat mass (g) (dotted line at 1.0 represents parameter for LFD and dotted line at 3.3 represents parameter for obese-HFD). d Pearson correlation analysis showing that the change in weight or fat mass fold change both negatively correlate to trabecular bone loss. e Correlation matrix that shows the change in weight or fat mass fold change both negatively correlate to trabecular bone loss (vertical line and horizontal line represent obesity cutoff). f Glucose tolerance test (GTT) for LFD ( n = 26), obese HFD-fed (OB-HFD; n = 34) and non-obese HFD-fed (NO-HFD; n = 7). g Insulin tolerance test (ITT) for LFD, obese HFD-fed (OB-HFD), and non-obese HFD-fed (NO-HFD). h <t>Serum</t> <t>adiponectin</t> levels ( n = 7). i Serum <t>leptin</t> levels. j Serum procollagen type I N-propeptide (P1NP) levels. k Serum tartrate-resistant acid phosphatase 5b (TRAcP 5b) levels. Analyses for a , f , and g were performed as 2-way ANOVA with Šídák’s multiple comparisons test. Significance for the post-hoc analysis for f , g was defined as: * P < 0.05 LFD vs. OB-HFD, # P < 0.05 LFD vs. NO-HFD-fed, and $ P < 0.05 OB-HFD vs. NO - HFD-fed. Analyses for h , i and k were performed as a Kruskal-Wallis test with Dunn’s multiple comparison. Analysis for j was performed as a One-way ANOVA with Tukey’s multiple comparisons test
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    Image Search Results


    Obesity parameters and metabolic phenotype in male B6 mice. a Body weight (g) measurements over 12 weeks for LFD and HFD-fed male B6 mice ( n = 32-41). b Change in weight (%) (dotted line at 28% represents parameter for LFD and dotted line at 58% represents parameter for HFD). c Fold change in fat mass (g) (dotted line at 1.0 represents parameter for LFD and dotted line at 3.3 represents parameter for obese-HFD). d Pearson correlation analysis showing that the change in weight or fat mass fold change both negatively correlate to trabecular bone loss. e Correlation matrix that shows the change in weight or fat mass fold change both negatively correlate to trabecular bone loss (vertical line and horizontal line represent obesity cutoff). f Glucose tolerance test (GTT) for LFD ( n = 26), obese HFD-fed (OB-HFD; n = 34) and non-obese HFD-fed (NO-HFD; n = 7). g Insulin tolerance test (ITT) for LFD, obese HFD-fed (OB-HFD), and non-obese HFD-fed (NO-HFD). h Serum adiponectin levels ( n = 7). i Serum leptin levels. j Serum procollagen type I N-propeptide (P1NP) levels. k Serum tartrate-resistant acid phosphatase 5b (TRAcP 5b) levels. Analyses for a , f , and g were performed as 2-way ANOVA with Šídák’s multiple comparisons test. Significance for the post-hoc analysis for f , g was defined as: * P < 0.05 LFD vs. OB-HFD, # P < 0.05 LFD vs. NO-HFD-fed, and $ P < 0.05 OB-HFD vs. NO - HFD-fed. Analyses for h , i and k were performed as a Kruskal-Wallis test with Dunn’s multiple comparison. Analysis for j was performed as a One-way ANOVA with Tukey’s multiple comparisons test

    Journal: Bone Research

    Article Title: Expansion of bone marrow adipocytes in obese mice leads to PD-L1-driven bone marrow immunosuppression and osteoclastogenesis

    doi: 10.1038/s41413-026-00509-5

    Figure Lengend Snippet: Obesity parameters and metabolic phenotype in male B6 mice. a Body weight (g) measurements over 12 weeks for LFD and HFD-fed male B6 mice ( n = 32-41). b Change in weight (%) (dotted line at 28% represents parameter for LFD and dotted line at 58% represents parameter for HFD). c Fold change in fat mass (g) (dotted line at 1.0 represents parameter for LFD and dotted line at 3.3 represents parameter for obese-HFD). d Pearson correlation analysis showing that the change in weight or fat mass fold change both negatively correlate to trabecular bone loss. e Correlation matrix that shows the change in weight or fat mass fold change both negatively correlate to trabecular bone loss (vertical line and horizontal line represent obesity cutoff). f Glucose tolerance test (GTT) for LFD ( n = 26), obese HFD-fed (OB-HFD; n = 34) and non-obese HFD-fed (NO-HFD; n = 7). g Insulin tolerance test (ITT) for LFD, obese HFD-fed (OB-HFD), and non-obese HFD-fed (NO-HFD). h Serum adiponectin levels ( n = 7). i Serum leptin levels. j Serum procollagen type I N-propeptide (P1NP) levels. k Serum tartrate-resistant acid phosphatase 5b (TRAcP 5b) levels. Analyses for a , f , and g were performed as 2-way ANOVA with Šídák’s multiple comparisons test. Significance for the post-hoc analysis for f , g was defined as: * P < 0.05 LFD vs. OB-HFD, # P < 0.05 LFD vs. NO-HFD-fed, and $ P < 0.05 OB-HFD vs. NO - HFD-fed. Analyses for h , i and k were performed as a Kruskal-Wallis test with Dunn’s multiple comparison. Analysis for j was performed as a One-way ANOVA with Tukey’s multiple comparisons test

    Article Snippet: Serum protein analysis of adiponectin (Mouse Adiponectin/Acrp30 Quantikine ELISA, R&D Systems MRP300), leptin (Mouse/Rat Leptin Quantikine ELISA, R&D Systems MOB00B), TRAP (Mousetrap TRAcP 5b ELISA, Immunodiagnostic Systems SB-TR103), CTX-1 (Mouse CTX ELISA Kit, Immunodiagnostic Systems AC-06F1), and P1NP (Rat/Mouse P1NP EIA, Immunodiagnostic Systems AC-33F1) were measured by ELISA according to manufacturer’s instructions.

    Techniques: Comparison