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ABclonal Biotechnology nephrin
Renal injury and associated biomarkers in the renal cortex of a postnatal hypoxia rat model. ( A ) Expression of the hypoxia marker HIF-1α in the renal cortex, quantified by average optical density (AOD), with HIF-1α-positive staining shown as brown coloration in IHC sections. Representative images were obtained at 200× magnification; scale bar = 50 μm. ( B ) Periodic acid–Schiff (PAS) staining of the renal cortex for the assessment of tubular injury scores, followed by quantitative analysis. Images were acquired at 200× magnification; scale bar = 50 μm. ( C ) Expression of the renal injury <t>marker</t> <t>NGAL</t> in the renal cortex, quantified by AOD, with NGAL-positive staining shown as brown coloration in IHC sections. Images were obtained at 200× magnification; scale bar = 50 μm. ( D ) Glomerular expression of <t>nephrin</t> in each group was quantified as the proportion of nephrin-positive area within the glomerulus, with nephrin staining shown as brown coloration in IHC sections. Images were obtained at 400× magnification; scale bar = 50 μm. For all panels, n = 6 per group. Data distribution was assessed using the Shapiro–Wilk normality test to determine whether parametric or non-parametric statistical analyses were applied. Parameters were analyzed using one-way ANOVA followed by the Sidak post hoc test, and are presented as mean ± SEM ( C , D ). Parameters were analyzed using the Kruskal–Wallis H test followed by Dunn’s post hoc test correction, and are presented as median (IQR) ( A , B ). * p < 0.05 versus normoxia groups (N7 and N14); # p < 0.05 versus H14. In the statistical figures, circles represent the N7 group, squares represent the H7 group, triangles represent the N14 group, inverted triangles represent the H14 group, and diamonds represent the H7N7 group. H7: neonatal rats exposed to hypoxia for 7 days after birth; H14: neonatal rats exposed to hypoxia for 14 days after birth; H7N7: neonatal rats exposed to hypoxia for 7 days followed by normoxia for 7 days; N7: neonatal rats maintained under normoxia for 7 days; N14: neonatal rats maintained under normoxia for 14 days; HIF-1α: hypoxia-inducible factor-1α; NGAL: neutrophil gelatinase-associated lipocalin.
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Image Search Results


Assay to detect nephrin autoantibodies.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Assay to detect nephrin autoantibodies.

Article Snippet: Separately, Streptavidin-coated plates were coated with 100 μL of biotinylated recombinant human nephrin capture protein (17757-H08H, Sino Biological), diluted 1:2000, and incubated at 37 °C with shaking at 700 rpm for 60–120 min.

Techniques:

Detection of serum anti-nephrin autoantibodies by ELISA. (a) Serum levels of anti-nephrin autoantibodies in patients with minimal change disease (MCD), primary focal segmental glomerulosclerosis (pFSGS), membranous nephropathy (MN), lupus nephritis (LN), diabetic nephropathy (DN), IgA nephropathy (IgAN), and healthy controls. (b) Positive rates of anti-nephrin autoantibodies in the same cohorts.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Detection of serum anti-nephrin autoantibodies by ELISA. (a) Serum levels of anti-nephrin autoantibodies in patients with minimal change disease (MCD), primary focal segmental glomerulosclerosis (pFSGS), membranous nephropathy (MN), lupus nephritis (LN), diabetic nephropathy (DN), IgA nephropathy (IgAN), and healthy controls. (b) Positive rates of anti-nephrin autoantibodies in the same cohorts.

Article Snippet: Separately, Streptavidin-coated plates were coated with 100 μL of biotinylated recombinant human nephrin capture protein (17757-H08H, Sino Biological), diluted 1:2000, and incubated at 37 °C with shaking at 700 rpm for 60–120 min.

Techniques: Enzyme-linked Immunosorbent Assay

Serum anti-nephrin autoantibody profiles across disease activity states in patients with MCD. (a) Serum levels of anti-nephrin autoantibodies in patients during active phase, partial remission (PR), and complete remission (CR). (b) Positivity rates of anti-nephrin autoantibodies across disease activity states. * p < 0.05, ** p < 0.01, *** p < 0.001.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Serum anti-nephrin autoantibody profiles across disease activity states in patients with MCD. (a) Serum levels of anti-nephrin autoantibodies in patients during active phase, partial remission (PR), and complete remission (CR). (b) Positivity rates of anti-nephrin autoantibodies across disease activity states. * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: Separately, Streptavidin-coated plates were coated with 100 μL of biotinylated recombinant human nephrin capture protein (17757-H08H, Sino Biological), diluted 1:2000, and incubated at 37 °C with shaking at 700 rpm for 60–120 min.

Techniques: Activity Assay

Correlations between serum anti-nephrin autoantibody levels and key clinical parameters.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Correlations between serum anti-nephrin autoantibody levels and key clinical parameters.

Article Snippet: Separately, Streptavidin-coated plates were coated with 100 μL of biotinylated recombinant human nephrin capture protein (17757-H08H, Sino Biological), diluted 1:2000, and incubated at 37 °C with shaking at 700 rpm for 60–120 min.

Techniques:

Comparison of clinical characteristics between patients positive and negative for anti-nephrin autoantibodies. * p < 0.05, ** p < 0.01, *** p < 0.001.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Comparison of clinical characteristics between patients positive and negative for anti-nephrin autoantibodies. * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: Separately, Streptavidin-coated plates were coated with 100 μL of biotinylated recombinant human nephrin capture protein (17757-H08H, Sino Biological), diluted 1:2000, and incubated at 37 °C with shaking at 700 rpm for 60–120 min.

Techniques: Comparison

Anti-nephrin autoantibody IgG subclasses in patients with MCD. (a) Proportion (%) of IgG subclasses among anti-nephrin autoantibodies. (b) Correlation of anti‑nephrin-IgG4 with total anti‑nephrin-IgG. (c) Ratios of anti-nephrin-IgG subclasses indicative of Th1/Th2 skewing: IgG1/IgG4 and IgG3/IgG4.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Anti-nephrin autoantibody IgG subclasses in patients with MCD. (a) Proportion (%) of IgG subclasses among anti-nephrin autoantibodies. (b) Correlation of anti‑nephrin-IgG4 with total anti‑nephrin-IgG. (c) Ratios of anti-nephrin-IgG subclasses indicative of Th1/Th2 skewing: IgG1/IgG4 and IgG3/IgG4.

Article Snippet: Separately, Streptavidin-coated plates were coated with 100 μL of biotinylated recombinant human nephrin capture protein (17757-H08H, Sino Biological), diluted 1:2000, and incubated at 37 °C with shaking at 700 rpm for 60–120 min.

Techniques:

Renal injury and associated biomarkers in the renal cortex of a postnatal hypoxia rat model. ( A ) Expression of the hypoxia marker HIF-1α in the renal cortex, quantified by average optical density (AOD), with HIF-1α-positive staining shown as brown coloration in IHC sections. Representative images were obtained at 200× magnification; scale bar = 50 μm. ( B ) Periodic acid–Schiff (PAS) staining of the renal cortex for the assessment of tubular injury scores, followed by quantitative analysis. Images were acquired at 200× magnification; scale bar = 50 μm. ( C ) Expression of the renal injury marker NGAL in the renal cortex, quantified by AOD, with NGAL-positive staining shown as brown coloration in IHC sections. Images were obtained at 200× magnification; scale bar = 50 μm. ( D ) Glomerular expression of nephrin in each group was quantified as the proportion of nephrin-positive area within the glomerulus, with nephrin staining shown as brown coloration in IHC sections. Images were obtained at 400× magnification; scale bar = 50 μm. For all panels, n = 6 per group. Data distribution was assessed using the Shapiro–Wilk normality test to determine whether parametric or non-parametric statistical analyses were applied. Parameters were analyzed using one-way ANOVA followed by the Sidak post hoc test, and are presented as mean ± SEM ( C , D ). Parameters were analyzed using the Kruskal–Wallis H test followed by Dunn’s post hoc test correction, and are presented as median (IQR) ( A , B ). * p < 0.05 versus normoxia groups (N7 and N14); # p < 0.05 versus H14. In the statistical figures, circles represent the N7 group, squares represent the H7 group, triangles represent the N14 group, inverted triangles represent the H14 group, and diamonds represent the H7N7 group. H7: neonatal rats exposed to hypoxia for 7 days after birth; H14: neonatal rats exposed to hypoxia for 14 days after birth; H7N7: neonatal rats exposed to hypoxia for 7 days followed by normoxia for 7 days; N7: neonatal rats maintained under normoxia for 7 days; N14: neonatal rats maintained under normoxia for 14 days; HIF-1α: hypoxia-inducible factor-1α; NGAL: neutrophil gelatinase-associated lipocalin.

Journal: Antioxidants

Article Title: Dynamic Regulation of Ferroptosis in a Neonatal Rat Model of Postnatal Hypoxia-Induced Acute Kidney Injury

doi: 10.3390/antiox15050582

Figure Lengend Snippet: Renal injury and associated biomarkers in the renal cortex of a postnatal hypoxia rat model. ( A ) Expression of the hypoxia marker HIF-1α in the renal cortex, quantified by average optical density (AOD), with HIF-1α-positive staining shown as brown coloration in IHC sections. Representative images were obtained at 200× magnification; scale bar = 50 μm. ( B ) Periodic acid–Schiff (PAS) staining of the renal cortex for the assessment of tubular injury scores, followed by quantitative analysis. Images were acquired at 200× magnification; scale bar = 50 μm. ( C ) Expression of the renal injury marker NGAL in the renal cortex, quantified by AOD, with NGAL-positive staining shown as brown coloration in IHC sections. Images were obtained at 200× magnification; scale bar = 50 μm. ( D ) Glomerular expression of nephrin in each group was quantified as the proportion of nephrin-positive area within the glomerulus, with nephrin staining shown as brown coloration in IHC sections. Images were obtained at 400× magnification; scale bar = 50 μm. For all panels, n = 6 per group. Data distribution was assessed using the Shapiro–Wilk normality test to determine whether parametric or non-parametric statistical analyses were applied. Parameters were analyzed using one-way ANOVA followed by the Sidak post hoc test, and are presented as mean ± SEM ( C , D ). Parameters were analyzed using the Kruskal–Wallis H test followed by Dunn’s post hoc test correction, and are presented as median (IQR) ( A , B ). * p < 0.05 versus normoxia groups (N7 and N14); # p < 0.05 versus H14. In the statistical figures, circles represent the N7 group, squares represent the H7 group, triangles represent the N14 group, inverted triangles represent the H14 group, and diamonds represent the H7N7 group. H7: neonatal rats exposed to hypoxia for 7 days after birth; H14: neonatal rats exposed to hypoxia for 14 days after birth; H7N7: neonatal rats exposed to hypoxia for 7 days followed by normoxia for 7 days; N7: neonatal rats maintained under normoxia for 7 days; N14: neonatal rats maintained under normoxia for 14 days; HIF-1α: hypoxia-inducible factor-1α; NGAL: neutrophil gelatinase-associated lipocalin.

Article Snippet: Primary antibodies included rabbit anti-mouse Alox-12 (1:200; ABclonal, Woburn, MA, USA; A14703), ferritin heavy chain (1:3000; ABclonal; A1144), ferritin light chain (1:100; ABclonal; A21758), FGF-23 (1:200; Bioss, Woburn, MA, USA; bs-5768R), HIF-1α (1:500; Proteintech, Rosemont, IL, USA; A23150), Klotho (1:200; Proteintech; 28100-1-AP), NGAL (1:1000; Abcam; ab63929) and nephrin (1:200; A23150; ABclonal).

Techniques: Expressing, Marker, Staining

Assay to detect nephrin autoantibodies.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Assay to detect nephrin autoantibodies.

Article Snippet: Biotinylated recombinant human nephrin detection protein (17757-H08H, Sino Biological), diluted 1:20,000, was added to the Protein G plates (100 μL/well) and incubated at 37 °C with shaking at 700 rpm for 60 ± 5 min, followed by washing three times with PBST.

Techniques:

Detection of serum anti-nephrin autoantibodies by ELISA. (a) Serum levels of anti-nephrin autoantibodies in patients with minimal change disease (MCD), primary focal segmental glomerulosclerosis (pFSGS), membranous nephropathy (MN), lupus nephritis (LN), diabetic nephropathy (DN), IgA nephropathy (IgAN), and healthy controls. (b) Positive rates of anti-nephrin autoantibodies in the same cohorts.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Detection of serum anti-nephrin autoantibodies by ELISA. (a) Serum levels of anti-nephrin autoantibodies in patients with minimal change disease (MCD), primary focal segmental glomerulosclerosis (pFSGS), membranous nephropathy (MN), lupus nephritis (LN), diabetic nephropathy (DN), IgA nephropathy (IgAN), and healthy controls. (b) Positive rates of anti-nephrin autoantibodies in the same cohorts.

Article Snippet: Biotinylated recombinant human nephrin detection protein (17757-H08H, Sino Biological), diluted 1:20,000, was added to the Protein G plates (100 μL/well) and incubated at 37 °C with shaking at 700 rpm for 60 ± 5 min, followed by washing three times with PBST.

Techniques: Enzyme-linked Immunosorbent Assay

Serum anti-nephrin autoantibody profiles across disease activity states in patients with MCD. (a) Serum levels of anti-nephrin autoantibodies in patients during active phase, partial remission (PR), and complete remission (CR). (b) Positivity rates of anti-nephrin autoantibodies across disease activity states. * p < 0.05, ** p < 0.01, *** p < 0.001.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Serum anti-nephrin autoantibody profiles across disease activity states in patients with MCD. (a) Serum levels of anti-nephrin autoantibodies in patients during active phase, partial remission (PR), and complete remission (CR). (b) Positivity rates of anti-nephrin autoantibodies across disease activity states. * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: Biotinylated recombinant human nephrin detection protein (17757-H08H, Sino Biological), diluted 1:20,000, was added to the Protein G plates (100 μL/well) and incubated at 37 °C with shaking at 700 rpm for 60 ± 5 min, followed by washing three times with PBST.

Techniques: Activity Assay

Correlations between serum anti-nephrin autoantibody levels and key clinical parameters.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Correlations between serum anti-nephrin autoantibody levels and key clinical parameters.

Article Snippet: Biotinylated recombinant human nephrin detection protein (17757-H08H, Sino Biological), diluted 1:20,000, was added to the Protein G plates (100 μL/well) and incubated at 37 °C with shaking at 700 rpm for 60 ± 5 min, followed by washing three times with PBST.

Techniques:

Comparison of clinical characteristics between patients positive and negative for anti-nephrin autoantibodies. * p < 0.05, ** p < 0.01, *** p < 0.001.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Comparison of clinical characteristics between patients positive and negative for anti-nephrin autoantibodies. * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: Biotinylated recombinant human nephrin detection protein (17757-H08H, Sino Biological), diluted 1:20,000, was added to the Protein G plates (100 μL/well) and incubated at 37 °C with shaking at 700 rpm for 60 ± 5 min, followed by washing three times with PBST.

Techniques: Comparison

Anti-nephrin autoantibody IgG subclasses in patients with MCD. (a) Proportion (%) of IgG subclasses among anti-nephrin autoantibodies. (b) Correlation of anti‑nephrin-IgG4 with total anti‑nephrin-IgG. (c) Ratios of anti-nephrin-IgG subclasses indicative of Th1/Th2 skewing: IgG1/IgG4 and IgG3/IgG4.

Journal: Annals of Medicine

Article Title: Association between anti-nephrin autoantibodies and disease activity in minimal change disease

doi: 10.1080/07853890.2026.2661115

Figure Lengend Snippet: Anti-nephrin autoantibody IgG subclasses in patients with MCD. (a) Proportion (%) of IgG subclasses among anti-nephrin autoantibodies. (b) Correlation of anti‑nephrin-IgG4 with total anti‑nephrin-IgG. (c) Ratios of anti-nephrin-IgG subclasses indicative of Th1/Th2 skewing: IgG1/IgG4 and IgG3/IgG4.

Article Snippet: Biotinylated recombinant human nephrin detection protein (17757-H08H, Sino Biological), diluted 1:20,000, was added to the Protein G plates (100 μL/well) and incubated at 37 °C with shaking at 700 rpm for 60 ± 5 min, followed by washing three times with PBST.

Techniques: