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human insulin-specific elisa kit  (Mercodia Inc)

 
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    Mercodia Inc human insulin-specific elisa kit
    Human Insulin Specific Elisa Kit, supplied by Mercodia Inc, 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/human+insulin-specific+elisa+kit/mouse+insulin+elisa+kit/pm33906910-43-10-12
    Average 90 stars, based on 1 article reviews
    human insulin-specific elisa kit - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: SEDDS for intestinal absorption of insulin: Application of Caco-2 and Caco-2/HT29 co-culture monolayers and intra-jejunal instillation in rats.
    Article Snippet: Accepted Manuscript SEDDS for intestinal absorption of insulin: Application of Caco-2 and Caco-2/ HT29 co-culture monolayers and intra-jejunal instillation in rats Jingying Liu, Ulrich Werner, Mario Funke, Melissa Besenius, Lasse Saaby, Mathias Fanø, Huiling Mu, Anette Müllertz PII: S0378-5173(19)30137-1 DOI: https://doi.org/10.1016/j.ijpharm.2019.02.014 Reference: IJP 18152 To appear in: International Journal of Pharmaceutics Received Date: 6 December 2018 Revised Date: 28 January 2019 Accepted Date: 12 February 2019 Please cite this article as: J. Liu, U. Werner, M. Funke, M. Besenius, L. Saaby, M. Fanø, H. Mu, A. Müllertz, SEDDS for intestinal absorption of insulin: Application of Caco-2 and Caco-2/HT29 co-culture monolayers and intra-jejunal instillation in rats, International Journal of Pharmaceutics (2019), doi: https://doi.org/10.1016/j.ijpharm.. 2019.02.014 This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.

    Clinical Proteomics:

    Article Title: MEK/ERK Signaling in β-Cells Bifunctionally Regulates β-Cell Mass and Glucose-Stimulated Insulin Secretion Response to Maintain Glucose Homeostasis.
    Article Snippet: In diabetic pathology, insufficiency in b-cell mass, unable to meet peripheral insulin demand, and functional defects of individual b-cells in production of insulin are often concurrently observed, collectively causing hyperglycemia.. Here we show that the phosphorylation of ERK1/2 is significantly decreased in the islets of db/db mice as well as in those of a cohort of subjects with type 2 diabetes.. In mice with abrogation of ERK signaling in pancreatic b-cells through deletion of Mek1 and Mek2, glucose intolerance aggravates under high-fat diet– feeding conditions due to insufficient insulin production with lower b-cell proliferation and reduced b-cell mass, while in individual b-cells dampening of the number of insulin exocytosis events is observed, with the molecules involved in insulin exocytosis being less phosphorylated.

    Enzyme-linked Immunosorbent Assay:

    Article Title: MEK/ERK Signaling in β-Cells Bifunctionally Regulates β-Cell Mass and Glucose-Stimulated Insulin Secretion Response to Maintain Glucose Homeostasis.
    Article Snippet: In diabetic pathology, insufficiency in b-cell mass, unable to meet peripheral insulin demand, and functional defects of individual b-cells in production of insulin are often concurrently observed, collectively causing hyperglycemia.. Here we show that the phosphorylation of ERK1/2 is significantly decreased in the islets of db/db mice as well as in those of a cohort of subjects with type 2 diabetes.. In mice with abrogation of ERK signaling in pancreatic b-cells through deletion of Mek1 and Mek2, glucose intolerance aggravates under high-fat diet– feeding conditions due to insufficient insulin production with lower b-cell proliferation and reduced b-cell mass, while in individual b-cells dampening of the number of insulin exocytosis events is observed, with the molecules involved in insulin exocytosis being less phosphorylated.



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    Effect of different formulations on TEER. Notes: A, simple solution of regular human insulin (1.6 mg/mL); B, simple solution of aspart insulin (1.6 mg/mL); C, dispersion of plain CS NPs (10 mg/mL); D, CPP-conjugated CS NPs loaded with regular human insulin (10 mg/mL); E, CPP-conjugated CS NPs loaded with aspart insulin (10 mg/mL); F, simple solution of CPP (PenetraMax; 10 µM/mL). Abbreviations: CPP, cell-penetrating peptide; CS, chitosan; NPs, nanoparticles; TEER, transepithelial electrical resistance.

    Journal: International Journal of Nanomedicine

    Article Title: A novel nanoemulsion-based method to produce ultrasmall, water-dispersible nanoparticles from chitosan, surface modified with cell-penetrating peptide for oral delivery of proteins and peptides

    doi: 10.2147/IJN.S116063

    Figure Lengend Snippet: Effect of different formulations on TEER. Notes: A, simple solution of regular human insulin (1.6 mg/mL); B, simple solution of aspart insulin (1.6 mg/mL); C, dispersion of plain CS NPs (10 mg/mL); D, CPP-conjugated CS NPs loaded with regular human insulin (10 mg/mL); E, CPP-conjugated CS NPs loaded with aspart insulin (10 mg/mL); F, simple solution of CPP (PenetraMax; 10 µM/mL). Abbreviations: CPP, cell-penetrating peptide; CS, chitosan; NPs, nanoparticles; TEER, transepithelial electrical resistance.

    Article Snippet: Aliquots were taken from the receiver chamber at predetermined time intervals and continued for 4 h, and the samples were investigated for insulin content with a special ELISA kit specific and sensitive to both regular human insulin and aspart insulin (Alpha Diagnostic International).

    Techniques:

    Cumulative transported insulin from different formulations. Notes: A, CPP-conjugated CS NPs loaded with regular human insulin (10 mg/mL); B, CPP-conjugated CS NPs loaded with aspart insulin (10 mg/mL); C, dispersion of plain CS NPs loaded with regular human insulin (10 mg/mL); D, simple solution of regular human insulin (1.6 mg/mL); E, simple solution of aspart insulin (1.6 mg/mL); F, dispersion of plain CS NPs loaded with aspart insulin (10 mg/mL). Abbreviations: CPP, cell-penetrating peptide; CS, chitosan; NPs, nanoparticles.

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    Article Title: A novel nanoemulsion-based method to produce ultrasmall, water-dispersible nanoparticles from chitosan, surface modified with cell-penetrating peptide for oral delivery of proteins and peptides

    doi: 10.2147/IJN.S116063

    Figure Lengend Snippet: Cumulative transported insulin from different formulations. Notes: A, CPP-conjugated CS NPs loaded with regular human insulin (10 mg/mL); B, CPP-conjugated CS NPs loaded with aspart insulin (10 mg/mL); C, dispersion of plain CS NPs loaded with regular human insulin (10 mg/mL); D, simple solution of regular human insulin (1.6 mg/mL); E, simple solution of aspart insulin (1.6 mg/mL); F, dispersion of plain CS NPs loaded with aspart insulin (10 mg/mL). Abbreviations: CPP, cell-penetrating peptide; CS, chitosan; NPs, nanoparticles.

    Article Snippet: Aliquots were taken from the receiver chamber at predetermined time intervals and continued for 4 h, and the samples were investigated for insulin content with a special ELISA kit specific and sensitive to both regular human insulin and aspart insulin (Alpha Diagnostic International).

    Techniques: