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mouse albumin assaymax elisa kit  (Assaypro)


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    Structured Review

    Assaypro mouse albumin assaymax elisa kit
    AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available <t>ELISA</t> kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.
    Mouse Albumin Assaymax Elisa Kit, 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/mouse+albumin+assaymax+elisa+kit/Mouse+Albumin+AssayMax+ELISA+Kit/pmc12786291-161-9-14
    Average 94 stars, based on 56 article reviews
    mouse albumin assaymax elisa kit - by Bioz Stars, 2026-09
    94/100 stars

    Images

    1) Product Images from "Metabolic and Antioxidant Modulation by Artemisia indica Willd. Aqueous Extract in Glucose and Cholesterol Dysregulation"

    Article Title: Metabolic and Antioxidant Modulation by Artemisia indica Willd. Aqueous Extract in Glucose and Cholesterol Dysregulation

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms27010297

    AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available ELISA kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.
    Figure Legend Snippet: AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available ELISA kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.

    Techniques Used: Activity Assay, Enzyme-linked Immunosorbent Assay, Staining, Derivative Assay, Control

    AAE enhanced antioxidant defense in HFD/STZ mice. The content of antioxidant enzymes, including glutathione (GSH) ( a ), superoxide dismutase (SOD) ( b ), and catalase ( c ), was detected by ELISA assays. ( d ) Malondialdehyde (MDA). Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; STZ: streptozotocin.
    Figure Legend Snippet: AAE enhanced antioxidant defense in HFD/STZ mice. The content of antioxidant enzymes, including glutathione (GSH) ( a ), superoxide dismutase (SOD) ( b ), and catalase ( c ), was detected by ELISA assays. ( d ) Malondialdehyde (MDA). Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; STZ: streptozotocin.

    Techniques Used: Enzyme-linked Immunosorbent Assay, Derivative Assay, Control

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    Article Title: Validation of Clinical-Grade Electroporation Systems for CRISPR-Cas9-Mediated Gene Therapy in Primary Hepatocytes for the Correction of Inherited Metabolic Liver Disease.
    Article Snippet: .. Conditioned media were collected from the plated cells at 24 h after plating to quantify the secreted albumin using an AssayPro Mouse Albumin AssayMax ELISA kit (EMA3201-1, AssayPro, St. Charles, MO, USA). .. At 24 h after plating, the hepatocytes were assessed for cell viability using a CyQUANT MTT Cell Viability Assay (V13154, Thermo Fisher Scientific).

    Article Title: RNF43/ZNRF3 loss predisposes to hepatocellular-carcinoma by impairing liver regeneration and altering the liver lipid metabolic ground-state
    Article Snippet: .. Finally, 24 h before collection, media was changed and the eventual supernatant was collected for measuring albumin secretion using the Mouse Albumin AssayMax ELISA Kit (Assay Pro). ..

    Article Title: Metabolic and Antioxidant Modulation by Artemisia indica Willd. Aqueous Extract in Glucose and Cholesterol Dysregulation
    Article Snippet: .. A normalized analysis was conducted by measuring urinary albumin (Mouse Albumin AssayMax ELISA Kit, Assaypro, Saint Charles, MO, USA, Cat# EMA3201-1) and urinary creatinine (Cayman Creatinine ELISA Kit, Item No. 502330, Michigan, USA), and subsequently, the urinary albumin-to-creatinine ratio (UACR) was calculated [ ]. .. Following the manufacturer’s instructions [ ], carboxymethyl-lysine (CML) was measured in the serum using competitive ELISA kits (OxiSelect Methylglyoxal Competitive ELISA Kit and OxiSelect N-epsilon-(Carboxymethyl) Lysine Competitive ELISA Kit, purchased from CELL BIOLABS Inc. (San Diego, CA, USA)).

    Article Title: Validation of Clinical-Grade Electroporation Systems for CRISPR-Cas9-Mediated Gene Therapy in Primary Hepatocytes for the Correction of Inherited Metabolic Liver Disease
    Article Snippet: .. Conditioned media were collected from the plated cells at 24 h after plating to quantify the secreted albumin using an AssayPro Mouse Albumin AssayMax ELISA kit (EMA3201-1, AssayPro, St. Charles, MO, USA). .. At 24 h after plating, the hepatocytes were assessed for cell viability using a CyQUANT MTT Cell Viability Assay (V13154, Thermo Fisher Scientific).



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    AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available <t>ELISA</t> kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.
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    AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available <t>ELISA</t> kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.
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    AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available <t>ELISA</t> kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.
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    AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available <t>ELISA</t> kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.
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    Assaypro mouse albumin elisa kit
    AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available <t>ELISA</t> kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.
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    Sickle cell disease (SCD) mice have albuminuria when they reach 4 months old. (A) At 2 months old, there was no significant difference in urinary albumin excretion between SCD and C57BL/6 mice ( n = 3, 2 males and 1 female in each strain). (B) By the age of 4 months, SCD mice exhibited a more than threefold increase in urinary albumin excretion compared to their levels at 2 months old (* p < 0.05, n = 5, 2 males and 3 females). It is worth noting that the disparities in urinary albumin levels observed between (A,B) for 2-month-old SCD mice are likely attributable to variations in measurement times and the use of different sets of SCD mice for each measurement. Urinary albumin levels were quantified using an <t>ELISA</t> kit <t>(EMA3201,</t> AssayPro). (C) SCD mice showed significantly elevated transcutaneous glomerular filtration rate (tGFR) compared to C57BL/6 mice (* p < 0.05, t -test, n = 5, 2 males and 3 females). The tGFR was determined by measuring the disappearance of fluorescein isothiocyanate (FITC)-sinistrin from the mouse body. (D) At 4 months old, SCD mice displayed enlarged glomeruli and minor fibrosis (indicated by arrows) compared to non-SCD mice (heterozygotes), as shown in representatives from three independent experiments. H & E, hematoxylin-eosin staining; MTC, Masson’s trichrome staining.
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    Assaypro mouse urine albumin levels
    Sickle cell disease (SCD) mice have albuminuria when they reach 4 months old. (A) At 2 months old, there was no significant difference in urinary albumin excretion between SCD and C57BL/6 mice ( n = 3, 2 males and 1 female in each strain). (B) By the age of 4 months, SCD mice exhibited a more than threefold increase in urinary albumin excretion compared to their levels at 2 months old (* p < 0.05, n = 5, 2 males and 3 females). It is worth noting that the disparities in urinary albumin levels observed between (A,B) for 2-month-old SCD mice are likely attributable to variations in measurement times and the use of different sets of SCD mice for each measurement. Urinary albumin levels were quantified using an <t>ELISA</t> kit <t>(EMA3201,</t> AssayPro). (C) SCD mice showed significantly elevated transcutaneous glomerular filtration rate (tGFR) compared to C57BL/6 mice (* p < 0.05, t -test, n = 5, 2 males and 3 females). The tGFR was determined by measuring the disappearance of fluorescein isothiocyanate (FITC)-sinistrin from the mouse body. (D) At 4 months old, SCD mice displayed enlarged glomeruli and minor fibrosis (indicated by arrows) compared to non-SCD mice (heterozygotes), as shown in representatives from three independent experiments. H & E, hematoxylin-eosin staining; MTC, Masson’s trichrome staining.
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    Image Search Results


    AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available ELISA kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.

    Journal: International Journal of Molecular Sciences

    Article Title: Metabolic and Antioxidant Modulation by Artemisia indica Willd. Aqueous Extract in Glucose and Cholesterol Dysregulation

    doi: 10.3390/ijms27010297

    Figure Lengend Snippet: AAE inhibited polyol pathway activity and glycogen accumulation in HFD/STZ mice. The levels of aldose reductase ( a ), fructose ( b ), methylglyoxal ( c ), and carboxymethyl-lysine ( d ) were detected by a commercially available ELISA kit. ( e ) Pathological changes were evaluated by periodic acid–Schiff (PAS) staining, showing glycogen accumulation and abnormal polysaccharides (400× magnification). ( f ) PAS-positive areas in kidney tissues were quantified. Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; * p < 0.05, ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; PAS: periodic acid–Schiff; STZ: streptozotocin.

    Article Snippet: A normalized analysis was conducted by measuring urinary albumin (Mouse Albumin AssayMax ELISA Kit, Assaypro, Saint Charles, MO, USA, Cat# EMA3201-1) and urinary creatinine (Cayman Creatinine ELISA Kit, Item No. 502330, Michigan, USA), and subsequently, the urinary albumin-to-creatinine ratio (UACR) was calculated [ ].

    Techniques: Activity Assay, Enzyme-linked Immunosorbent Assay, Staining, Derivative Assay, Control

    AAE enhanced antioxidant defense in HFD/STZ mice. The content of antioxidant enzymes, including glutathione (GSH) ( a ), superoxide dismutase (SOD) ( b ), and catalase ( c ), was detected by ELISA assays. ( d ) Malondialdehyde (MDA). Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; STZ: streptozotocin.

    Journal: International Journal of Molecular Sciences

    Article Title: Metabolic and Antioxidant Modulation by Artemisia indica Willd. Aqueous Extract in Glucose and Cholesterol Dysregulation

    doi: 10.3390/ijms27010297

    Figure Lengend Snippet: AAE enhanced antioxidant defense in HFD/STZ mice. The content of antioxidant enzymes, including glutathione (GSH) ( a ), superoxide dismutase (SOD) ( b ), and catalase ( c ), was detected by ELISA assays. ( d ) Malondialdehyde (MDA). Data were collected per group and are presented as the mean ± SD ( n = 5), derived from five independent biological replicates. # p < 0.05, ## p < 0.01 versus the control group; ** p < 0.01 versus the model group. AAE: Artemisia indica Willd. aqueous extract; HFD: high-fat diet; STZ: streptozotocin.

    Article Snippet: A normalized analysis was conducted by measuring urinary albumin (Mouse Albumin AssayMax ELISA Kit, Assaypro, Saint Charles, MO, USA, Cat# EMA3201-1) and urinary creatinine (Cayman Creatinine ELISA Kit, Item No. 502330, Michigan, USA), and subsequently, the urinary albumin-to-creatinine ratio (UACR) was calculated [ ].

    Techniques: Enzyme-linked Immunosorbent Assay, Derivative Assay, Control

    Sickle cell disease (SCD) mice have albuminuria when they reach 4 months old. (A) At 2 months old, there was no significant difference in urinary albumin excretion between SCD and C57BL/6 mice ( n = 3, 2 males and 1 female in each strain). (B) By the age of 4 months, SCD mice exhibited a more than threefold increase in urinary albumin excretion compared to their levels at 2 months old (* p < 0.05, n = 5, 2 males and 3 females). It is worth noting that the disparities in urinary albumin levels observed between (A,B) for 2-month-old SCD mice are likely attributable to variations in measurement times and the use of different sets of SCD mice for each measurement. Urinary albumin levels were quantified using an ELISA kit (EMA3201, AssayPro). (C) SCD mice showed significantly elevated transcutaneous glomerular filtration rate (tGFR) compared to C57BL/6 mice (* p < 0.05, t -test, n = 5, 2 males and 3 females). The tGFR was determined by measuring the disappearance of fluorescein isothiocyanate (FITC)-sinistrin from the mouse body. (D) At 4 months old, SCD mice displayed enlarged glomeruli and minor fibrosis (indicated by arrows) compared to non-SCD mice (heterozygotes), as shown in representatives from three independent experiments. H & E, hematoxylin-eosin staining; MTC, Masson’s trichrome staining.

    Journal: Frontiers in Physiology

    Article Title: Proteomic analyses of urinary exosomes identify novel potential biomarkers for early diagnosis of sickle cell nephropathy, a sex-based study

    doi: 10.3389/fphys.2024.1300667

    Figure Lengend Snippet: Sickle cell disease (SCD) mice have albuminuria when they reach 4 months old. (A) At 2 months old, there was no significant difference in urinary albumin excretion between SCD and C57BL/6 mice ( n = 3, 2 males and 1 female in each strain). (B) By the age of 4 months, SCD mice exhibited a more than threefold increase in urinary albumin excretion compared to their levels at 2 months old (* p < 0.05, n = 5, 2 males and 3 females). It is worth noting that the disparities in urinary albumin levels observed between (A,B) for 2-month-old SCD mice are likely attributable to variations in measurement times and the use of different sets of SCD mice for each measurement. Urinary albumin levels were quantified using an ELISA kit (EMA3201, AssayPro). (C) SCD mice showed significantly elevated transcutaneous glomerular filtration rate (tGFR) compared to C57BL/6 mice (* p < 0.05, t -test, n = 5, 2 males and 3 females). The tGFR was determined by measuring the disappearance of fluorescein isothiocyanate (FITC)-sinistrin from the mouse body. (D) At 4 months old, SCD mice displayed enlarged glomeruli and minor fibrosis (indicated by arrows) compared to non-SCD mice (heterozygotes), as shown in representatives from three independent experiments. H & E, hematoxylin-eosin staining; MTC, Masson’s trichrome staining.

    Article Snippet: Mouse urine albumin levels were measured using the Mouse Albumin Assay Max ELISA kit (catalog # EMA3201-1 from AssayPro) according to the manufacturer’s protocol.

    Techniques: Enzyme-linked Immunosorbent Assay, Filtration, Staining