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mouse urine albumin levels  (Assaypro)


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    Assaypro mouse urine albumin levels
    Mouse Urine Albumin Levels, supplied by Assaypro, used in various techniques. Bioz Stars score: 94/100, based on 56 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/urine+albumin+levels/Mouse+Albumin+AssayMax+ELISA+Kit/pmc10901968-68-0-18
    Average 94 stars, based on 56 article reviews
    mouse urine albumin levels - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Prevention of diabetic nephropathy in Ins2 +/−AkitaJ mice by the mitochondria-targeted therapy MitoQ
    Article Snippet: Urine from the experimental animals was collected for 24 h on ice using diuresis cages (Tecniplast) and the volumes were determined. .. Urine albumin levels were determined using a mouse-specific ELISA system for urine albumin (EMA3201-1; AssayPro) and was calculated as the total amount of albumin excreted per day. ..

    Article Title: Prevention of diabetic nephropathy in Ins2+/−AkitaJ mice by the mitochondria-targeted therapy MitoQ
    Article Snippet: Urine collection and estimation of urine albumin Urine from the experimental animals was collected for 24 h on ice using diuresis cages (Tecniplast) and the volumes were determined. .. Urine albumin levels were determined using a mouse-specific ELISA system for urine albumin (EMA3201-1; AssayPro) and was calculated as the total amount of albumin excreted per day. ..

    Article Title: Simvastatin ameliorates diabetic nephropathy by attenuating oxidative stress and apoptosis in a rat model of streptozotocin-induced type 1 diabetes.
    Article Snippet: Statins are HMG-CoA reductase inhibitors with lipid-lowering effect and commonly used to reduce cardiovascular risk in diabetic patients.. The present study investigates the ameliorative effect of simvastatin (SIM) on diabetic nephropathy in rats, pointing to its anti-apoptotic and anti-oxidative stress efficacies.. Diabetes was induced by a single intraperitoneal injection of 55mg/kg body weight streptozotocin (STZ) and both control and diabetic rats received 10mg/kg SIM for 90 days.



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    ( A ) Representative immunoblot images of profilin1 expression in primary podocytes freshly isolated from littermate control (Ctrl) and Pfn1 -KO <t>mice</t> (age P7). ( B ) Representative immunofluorescence images of profilin1 (green) and WT1 (red) in control and Pfn1 -KO primary podocytes. Scale bar: 10 μm. ( C ) Representative immunofluorescence images of profilin1 (green) and nephrin (red) on kidney sections of control and Pfn1- KO mice (age 3 weeks). Scale bars: 10 μm. ( D ) Pfn1- KO mice (red) failed to gain body weight by 8 weeks of age compared with control mice (green). n = 9 mice. * P < 0.05 vs. control. ( E ) The survival curve of Pfn1- KO mice (red) demonstrates approximately 90% death by 12 weeks of age. n = 8 mice. ( F ) SDS-PAGE (Coomassie blue staining) of standard BSA and of <t>urine</t> samples from Pfn1 -KO mice at 4 weeks of age demonstrates albuminuria. Equal volumes of standard BSA and urine (4 μL) were loaded in each lane. ( G ) Quantification of urine <t>albumin</t> normalized to creatinine at 2, 6, and 10 weeks of age. n = 6 mice. * P < 0.05 vs. control. ( H ) Elevated plasma creatinine in Pfn1- KO mice at 3, 6, and 10 weeks of age. * P < 0.05 vs. control. Statistics were analyzed via a 2-tailed t test.
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    ( A ) Representative immunoblot images of profilin1 expression in primary podocytes freshly isolated from littermate control (Ctrl) and Pfn1 -KO <t>mice</t> (age P7). ( B ) Representative immunofluorescence images of profilin1 (green) and WT1 (red) in control and Pfn1 -KO primary podocytes. Scale bar: 10 μm. ( C ) Representative immunofluorescence images of profilin1 (green) and nephrin (red) on kidney sections of control and Pfn1- KO mice (age 3 weeks). Scale bars: 10 μm. ( D ) Pfn1- KO mice (red) failed to gain body weight by 8 weeks of age compared with control mice (green). n = 9 mice. * P < 0.05 vs. control. ( E ) The survival curve of Pfn1- KO mice (red) demonstrates approximately 90% death by 12 weeks of age. n = 8 mice. ( F ) SDS-PAGE (Coomassie blue staining) of standard BSA and of <t>urine</t> samples from Pfn1 -KO mice at 4 weeks of age demonstrates albuminuria. Equal volumes of standard BSA and urine (4 μL) were loaded in each lane. ( G ) Quantification of urine <t>albumin</t> normalized to creatinine at 2, 6, and 10 weeks of age. n = 6 mice. * P < 0.05 vs. control. ( H ) Elevated plasma creatinine in Pfn1- KO mice at 3, 6, and 10 weeks of age. * P < 0.05 vs. control. Statistics were analyzed via a 2-tailed t test.
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    ( A ) Representative immunoblot images of profilin1 expression in primary podocytes freshly isolated from littermate control (Ctrl) and Pfn1 -KO <t>mice</t> (age P7). ( B ) Representative immunofluorescence images of profilin1 (green) and WT1 (red) in control and Pfn1 -KO primary podocytes. Scale bar: 10 μm. ( C ) Representative immunofluorescence images of profilin1 (green) and nephrin (red) on kidney sections of control and Pfn1- KO mice (age 3 weeks). Scale bars: 10 μm. ( D ) Pfn1- KO mice (red) failed to gain body weight by 8 weeks of age compared with control mice (green). n = 9 mice. * P < 0.05 vs. control. ( E ) The survival curve of Pfn1- KO mice (red) demonstrates approximately 90% death by 12 weeks of age. n = 8 mice. ( F ) SDS-PAGE (Coomassie blue staining) of standard BSA and of <t>urine</t> samples from Pfn1 -KO mice at 4 weeks of age demonstrates albuminuria. Equal volumes of standard BSA and urine (4 μL) were loaded in each lane. ( G ) Quantification of urine <t>albumin</t> normalized to creatinine at 2, 6, and 10 weeks of age. n = 6 mice. * P < 0.05 vs. control. ( H ) Elevated plasma creatinine in Pfn1- KO mice at 3, 6, and 10 weeks of age. * P < 0.05 vs. control. Statistics were analyzed via a 2-tailed t test.
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    ( A ) Representative immunoblot images of profilin1 expression in primary podocytes freshly isolated from littermate control (Ctrl) and Pfn1 -KO <t>mice</t> (age P7). ( B ) Representative immunofluorescence images of profilin1 (green) and WT1 (red) in control and Pfn1 -KO primary podocytes. Scale bar: 10 μm. ( C ) Representative immunofluorescence images of profilin1 (green) and nephrin (red) on kidney sections of control and Pfn1- KO mice (age 3 weeks). Scale bars: 10 μm. ( D ) Pfn1- KO mice (red) failed to gain body weight by 8 weeks of age compared with control mice (green). n = 9 mice. * P < 0.05 vs. control. ( E ) The survival curve of Pfn1- KO mice (red) demonstrates approximately 90% death by 12 weeks of age. n = 8 mice. ( F ) SDS-PAGE (Coomassie blue staining) of standard BSA and of <t>urine</t> samples from Pfn1 -KO mice at 4 weeks of age demonstrates albuminuria. Equal volumes of standard BSA and urine (4 μL) were loaded in each lane. ( G ) Quantification of urine <t>albumin</t> normalized to creatinine at 2, 6, and 10 weeks of age. n = 6 mice. * P < 0.05 vs. control. ( H ) Elevated plasma creatinine in Pfn1- KO mice at 3, 6, and 10 weeks of age. * P < 0.05 vs. control. Statistics were analyzed via a 2-tailed t test.
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    Image Search Results


    ( A ) Representative immunoblot images of profilin1 expression in primary podocytes freshly isolated from littermate control (Ctrl) and Pfn1 -KO mice (age P7). ( B ) Representative immunofluorescence images of profilin1 (green) and WT1 (red) in control and Pfn1 -KO primary podocytes. Scale bar: 10 μm. ( C ) Representative immunofluorescence images of profilin1 (green) and nephrin (red) on kidney sections of control and Pfn1- KO mice (age 3 weeks). Scale bars: 10 μm. ( D ) Pfn1- KO mice (red) failed to gain body weight by 8 weeks of age compared with control mice (green). n = 9 mice. * P < 0.05 vs. control. ( E ) The survival curve of Pfn1- KO mice (red) demonstrates approximately 90% death by 12 weeks of age. n = 8 mice. ( F ) SDS-PAGE (Coomassie blue staining) of standard BSA and of urine samples from Pfn1 -KO mice at 4 weeks of age demonstrates albuminuria. Equal volumes of standard BSA and urine (4 μL) were loaded in each lane. ( G ) Quantification of urine albumin normalized to creatinine at 2, 6, and 10 weeks of age. n = 6 mice. * P < 0.05 vs. control. ( H ) Elevated plasma creatinine in Pfn1- KO mice at 3, 6, and 10 weeks of age. * P < 0.05 vs. control. Statistics were analyzed via a 2-tailed t test.

    Journal: The Journal of Clinical Investigation

    Article Title: Profilin1 is required for prevention of mitotic catastrophe in murine and human glomerular diseases

    doi: 10.1172/JCI171237

    Figure Lengend Snippet: ( A ) Representative immunoblot images of profilin1 expression in primary podocytes freshly isolated from littermate control (Ctrl) and Pfn1 -KO mice (age P7). ( B ) Representative immunofluorescence images of profilin1 (green) and WT1 (red) in control and Pfn1 -KO primary podocytes. Scale bar: 10 μm. ( C ) Representative immunofluorescence images of profilin1 (green) and nephrin (red) on kidney sections of control and Pfn1- KO mice (age 3 weeks). Scale bars: 10 μm. ( D ) Pfn1- KO mice (red) failed to gain body weight by 8 weeks of age compared with control mice (green). n = 9 mice. * P < 0.05 vs. control. ( E ) The survival curve of Pfn1- KO mice (red) demonstrates approximately 90% death by 12 weeks of age. n = 8 mice. ( F ) SDS-PAGE (Coomassie blue staining) of standard BSA and of urine samples from Pfn1 -KO mice at 4 weeks of age demonstrates albuminuria. Equal volumes of standard BSA and urine (4 μL) were loaded in each lane. ( G ) Quantification of urine albumin normalized to creatinine at 2, 6, and 10 weeks of age. n = 6 mice. * P < 0.05 vs. control. ( H ) Elevated plasma creatinine in Pfn1- KO mice at 3, 6, and 10 weeks of age. * P < 0.05 vs. control. Statistics were analyzed via a 2-tailed t test.

    Article Snippet: Mouse urine albumin levels were measured in duplicate for each sample using an albumin ELISA quantification kit according to the manufacturer’s protocol (Bethyl Laboratories Inc.) at an absorbance of 450 nm.

    Techniques: Western Blot, Expressing, Isolation, Control, Immunofluorescence, SDS Page, Staining, Clinical Proteomics