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elisa kits for soluble rage  (Elabscience Biotechnology)


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    Elabscience Biotechnology elisa kits for soluble rage
    Elisa Kits For Soluble Rage, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/elisa+kits+for+soluble+rage/elisa+kits+for+soluble+rage/pm33548580-44-4-12
    Average 90 stars, based on 1 article reviews
    elisa kits for soluble rage - by Bioz Stars, 2026-09
    90/100 stars

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    Enzyme-linked Immunosorbent Assay:

    Article Title: The receptor for advanced glycation end products mediates dysfunction of airway epithelial barrier in a lipopolysaccharides-induced murine acute lung injury model.
    Article Snippet: Background: Airway epithelial cells (AECs) act as the first barrier protecting against invasion of environment agents and maintain integrity of lung structure and function.. Dysfunction of airway epithelial barrier has been shown to be involved in ALI/ARDS pathogenesis.. Yet, the exact mechanism is still obscure.



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    Elevation of high-mobility group box 1 (HMGB1) levels, and other serum levels, after autologous islet transplantation (AIT). Values for (A) HMGB1 (top), C-peptide (middle), and proinsulin (bottom) in 15 patients; data are expressed as mean ± SE. (B) HMGB1 serum levels after transplant with 100% purity islets. The curve is that of a single patient. (C) Soluble receptor for advanced glycation end products <t>(sRAGE)</t> in 15 patients; data are expressed as mean ± SE. *With repeated measurement of ANOVA, p < 0.05 compared to admission level.
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    Image Search Results


    Elevation of high-mobility group box 1 (HMGB1) levels, and other serum levels, after autologous islet transplantation (AIT). Values for (A) HMGB1 (top), C-peptide (middle), and proinsulin (bottom) in 15 patients; data are expressed as mean ± SE. (B) HMGB1 serum levels after transplant with 100% purity islets. The curve is that of a single patient. (C) Soluble receptor for advanced glycation end products (sRAGE) in 15 patients; data are expressed as mean ± SE. *With repeated measurement of ANOVA, p < 0.05 compared to admission level.

    Journal: Cell transplantation

    Article Title: Elevation of High-Mobility Group Box 1 After Clinical Autologous Islet Transplantation and Its Inverse Correlation With Outcomes

    doi: 10.3727/096368912X658980

    Figure Lengend Snippet: Elevation of high-mobility group box 1 (HMGB1) levels, and other serum levels, after autologous islet transplantation (AIT). Values for (A) HMGB1 (top), C-peptide (middle), and proinsulin (bottom) in 15 patients; data are expressed as mean ± SE. (B) HMGB1 serum levels after transplant with 100% purity islets. The curve is that of a single patient. (C) Soluble receptor for advanced glycation end products (sRAGE) in 15 patients; data are expressed as mean ± SE. *With repeated measurement of ANOVA, p < 0.05 compared to admission level.

    Article Snippet: The serum levels of HMGB1, C-peptide, proinsulin, and soluble receptor for glycation end products (sRAGE) were measured using HMGB1 ELISA kit II (Shino-test, Kanagawa, Japan) ( 37 ), C-peptide enzyme-linked immunosorbent assay (ELISA) kit (Mercodia, Uppsala, Sweden), proinsulin ELISA kit (Mercodia), and Quantikine human soluble RAGE kit (R&D Systems, Minneapolis, MN, USA), according to the manufacturers’ instructions.

    Techniques: Transplantation Assay

    The change in high-mobility group box 1 (HMGB1; A) and soluble receptor for advanced glycation end products (sRAGE; B) between admission and first peak levels in the autologous islet transplantation (AIT) group (n = 15) and the pancreatectomy-only control (Px; n = 3). The data are expressed as mean ± SE. *With Student’s t test, p < 0.05.

    Journal: Cell transplantation

    Article Title: Elevation of High-Mobility Group Box 1 After Clinical Autologous Islet Transplantation and Its Inverse Correlation With Outcomes

    doi: 10.3727/096368912X658980

    Figure Lengend Snippet: The change in high-mobility group box 1 (HMGB1; A) and soluble receptor for advanced glycation end products (sRAGE; B) between admission and first peak levels in the autologous islet transplantation (AIT) group (n = 15) and the pancreatectomy-only control (Px; n = 3). The data are expressed as mean ± SE. *With Student’s t test, p < 0.05.

    Article Snippet: The serum levels of HMGB1, C-peptide, proinsulin, and soluble receptor for glycation end products (sRAGE) were measured using HMGB1 ELISA kit II (Shino-test, Kanagawa, Japan) ( 37 ), C-peptide enzyme-linked immunosorbent assay (ELISA) kit (Mercodia, Uppsala, Sweden), proinsulin ELISA kit (Mercodia), and Quantikine human soluble RAGE kit (R&D Systems, Minneapolis, MN, USA), according to the manufacturers’ instructions.

    Techniques: Transplantation Assay, Control

    Release of high-mobility group box 1 (HMGB1), C-peptide, and proinsulin, but not soluble receptor for advanced glycation end products (sRAGE), by damaged human islets. (A) Control islets, cytokine-induced damaged islets, and hypoxia-induced damaged islets were stained with Hoechst33342 and propidium iodide (HO342/PI) (left), insulin (green), HMGB1 (red), and 4′,6-diamidino- 2-phenylindole (DAPI; blue). Scale bars: 100 μm. (B) ELISA measurements of the amount of released proinsulin, C-peptide, HMGB1, and sRAGE from the three groups of islets. The data are expressed as mean ± SD. *p < 0.05 compared to control. nd, not detected.

    Journal: Cell transplantation

    Article Title: Elevation of High-Mobility Group Box 1 After Clinical Autologous Islet Transplantation and Its Inverse Correlation With Outcomes

    doi: 10.3727/096368912X658980

    Figure Lengend Snippet: Release of high-mobility group box 1 (HMGB1), C-peptide, and proinsulin, but not soluble receptor for advanced glycation end products (sRAGE), by damaged human islets. (A) Control islets, cytokine-induced damaged islets, and hypoxia-induced damaged islets were stained with Hoechst33342 and propidium iodide (HO342/PI) (left), insulin (green), HMGB1 (red), and 4′,6-diamidino- 2-phenylindole (DAPI; blue). Scale bars: 100 μm. (B) ELISA measurements of the amount of released proinsulin, C-peptide, HMGB1, and sRAGE from the three groups of islets. The data are expressed as mean ± SD. *p < 0.05 compared to control. nd, not detected.

    Article Snippet: The serum levels of HMGB1, C-peptide, proinsulin, and soluble receptor for glycation end products (sRAGE) were measured using HMGB1 ELISA kit II (Shino-test, Kanagawa, Japan) ( 37 ), C-peptide enzyme-linked immunosorbent assay (ELISA) kit (Mercodia, Uppsala, Sweden), proinsulin ELISA kit (Mercodia), and Quantikine human soluble RAGE kit (R&D Systems, Minneapolis, MN, USA), according to the manufacturers’ instructions.

    Techniques: Control, Staining, Enzyme-linked Immunosorbent Assay

    Differences between the insulin-dependent group and insulin-free group after autologous islet transplantation (AIT). Results from patients with pretransplant glycated hemoglobin (HbA1c) <6.0% (n = 9) and ≥6.0% (n = 6) are shown in A to C and D to F, respectively. (A and D) The changes in high-mobility group box 1 (HMGB1) between admission and first peak levels and (B and E) the change in soluble receptor for advanced glycation end products (sRAGE) between admission and peak levels. Individual data and median bar are shown. *With Student’s t test p < 0.05. (C and F) Correlation between ΔHMGB1, ΔsRAGE, and insulin dependency. The white circles show insulin-free patients (n = 4; n = 3), and the black triangles show insulin-dependent patients (n = 5; n = 3) in C and F.

    Journal: Cell transplantation

    Article Title: Elevation of High-Mobility Group Box 1 After Clinical Autologous Islet Transplantation and Its Inverse Correlation With Outcomes

    doi: 10.3727/096368912X658980

    Figure Lengend Snippet: Differences between the insulin-dependent group and insulin-free group after autologous islet transplantation (AIT). Results from patients with pretransplant glycated hemoglobin (HbA1c) <6.0% (n = 9) and ≥6.0% (n = 6) are shown in A to C and D to F, respectively. (A and D) The changes in high-mobility group box 1 (HMGB1) between admission and first peak levels and (B and E) the change in soluble receptor for advanced glycation end products (sRAGE) between admission and peak levels. Individual data and median bar are shown. *With Student’s t test p < 0.05. (C and F) Correlation between ΔHMGB1, ΔsRAGE, and insulin dependency. The white circles show insulin-free patients (n = 4; n = 3), and the black triangles show insulin-dependent patients (n = 5; n = 3) in C and F.

    Article Snippet: The serum levels of HMGB1, C-peptide, proinsulin, and soluble receptor for glycation end products (sRAGE) were measured using HMGB1 ELISA kit II (Shino-test, Kanagawa, Japan) ( 37 ), C-peptide enzyme-linked immunosorbent assay (ELISA) kit (Mercodia, Uppsala, Sweden), proinsulin ELISA kit (Mercodia), and Quantikine human soluble RAGE kit (R&D Systems, Minneapolis, MN, USA), according to the manufacturers’ instructions.

    Techniques: Transplantation Assay

    Journal: Cell transplantation

    Article Title: Elevation of High-Mobility Group Box 1 After Clinical Autologous Islet Transplantation and Its Inverse Correlation With Outcomes

    doi: 10.3727/096368912X658980

    Figure Lengend Snippet: Correlation Between Fasting C-Peptide or SUITO Index and ΔHMGB1 or ΔsRAGE

    Article Snippet: The serum levels of HMGB1, C-peptide, proinsulin, and soluble receptor for glycation end products (sRAGE) were measured using HMGB1 ELISA kit II (Shino-test, Kanagawa, Japan) ( 37 ), C-peptide enzyme-linked immunosorbent assay (ELISA) kit (Mercodia, Uppsala, Sweden), proinsulin ELISA kit (Mercodia), and Quantikine human soluble RAGE kit (R&D Systems, Minneapolis, MN, USA), according to the manufacturers’ instructions.

    Techniques: