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nephrin  (Novus Biologicals)


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    Structured Review

    Novus Biologicals nephrin
    Nephrin, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nephrin/pm41990583-125-10-11?v=Novus+Biologicals
    Average 92 stars, based on 6 article reviews
    nephrin - by Bioz Stars, 2026-07
    92/100 stars

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    R&D Systems nephrin
    (a) OCT frozen kidney biopsies were sectioned, cleared <t>and</t> <t>immunolabelled</t> followed by confocal imaging and deep-learning segmentation. (b) Maximum intensity projection confocal image of <t>nephrin</t> visualizing the slit diaphragm network and foot processes. (c) Output of the semantic segmentation of both the slit diaphragm and foot processes. Foot processes are marked in red and the slit diaphragm in green. (d) Output of the instance segmentation resulting in segmentation of each individual foot process in the image. Each foot process is presented in an individual color. (e-g) From the 2 segmentation outputs, the morphometric parameters SDL (e), FP circularity (f), FP area and FP perimeter (g) are extracted. (e) Schematic image of how SDL is measured. The length of the slit (in blue) is divided by the surface area (outlined in white) resulting in a length-density measurement of slit coverage. (f) Schematic image of how FP circularity is measured. From the segmentation of the individual foot processes, the FP circularity is calculated using the formula, circularity = 4 π (area/perimeter−2). The result is a value between 0 and 1 where a perfect circle has a circularity of 1 and a very elongated rectangle approaches 0. (g) Foot process size is calculated both by FP area and by FP perimeter. The FP area is the pixel area of each segmented foot process converted to µm 2 and the FP perimeter is the outline of the foot process with it closed at the base.
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    Santa Cruz Biotechnology p nephrin
    (a) OCT frozen kidney biopsies were sectioned, cleared <t>and</t> <t>immunolabelled</t> followed by confocal imaging and deep-learning segmentation. (b) Maximum intensity projection confocal image of <t>nephrin</t> visualizing the slit diaphragm network and foot processes. (c) Output of the semantic segmentation of both the slit diaphragm and foot processes. Foot processes are marked in red and the slit diaphragm in green. (d) Output of the instance segmentation resulting in segmentation of each individual foot process in the image. Each foot process is presented in an individual color. (e-g) From the 2 segmentation outputs, the morphometric parameters SDL (e), FP circularity (f), FP area and FP perimeter (g) are extracted. (e) Schematic image of how SDL is measured. The length of the slit (in blue) is divided by the surface area (outlined in white) resulting in a length-density measurement of slit coverage. (f) Schematic image of how FP circularity is measured. From the segmentation of the individual foot processes, the FP circularity is calculated using the formula, circularity = 4 π (area/perimeter−2). The result is a value between 0 and 1 where a perfect circle has a circularity of 1 and a very elongated rectangle approaches 0. (g) Foot process size is calculated both by FP area and by FP perimeter. The FP area is the pixel area of each segmented foot process converted to µm 2 and the FP perimeter is the outline of the foot process with it closed at the base.
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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: 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:

    (a) OCT frozen kidney biopsies were sectioned, cleared and immunolabelled followed by confocal imaging and deep-learning segmentation. (b) Maximum intensity projection confocal image of nephrin visualizing the slit diaphragm network and foot processes. (c) Output of the semantic segmentation of both the slit diaphragm and foot processes. Foot processes are marked in red and the slit diaphragm in green. (d) Output of the instance segmentation resulting in segmentation of each individual foot process in the image. Each foot process is presented in an individual color. (e-g) From the 2 segmentation outputs, the morphometric parameters SDL (e), FP circularity (f), FP area and FP perimeter (g) are extracted. (e) Schematic image of how SDL is measured. The length of the slit (in blue) is divided by the surface area (outlined in white) resulting in a length-density measurement of slit coverage. (f) Schematic image of how FP circularity is measured. From the segmentation of the individual foot processes, the FP circularity is calculated using the formula, circularity = 4 π (area/perimeter−2). The result is a value between 0 and 1 where a perfect circle has a circularity of 1 and a very elongated rectangle approaches 0. (g) Foot process size is calculated both by FP area and by FP perimeter. The FP area is the pixel area of each segmented foot process converted to µm 2 and the FP perimeter is the outline of the foot process with it closed at the base.

    Journal: medRxiv

    Article Title: Nanoscale Podocyte Morphometrics Predict Disease Progression in IgA Nephropathy

    doi: 10.64898/2026.03.30.26349728

    Figure Lengend Snippet: (a) OCT frozen kidney biopsies were sectioned, cleared and immunolabelled followed by confocal imaging and deep-learning segmentation. (b) Maximum intensity projection confocal image of nephrin visualizing the slit diaphragm network and foot processes. (c) Output of the semantic segmentation of both the slit diaphragm and foot processes. Foot processes are marked in red and the slit diaphragm in green. (d) Output of the instance segmentation resulting in segmentation of each individual foot process in the image. Each foot process is presented in an individual color. (e-g) From the 2 segmentation outputs, the morphometric parameters SDL (e), FP circularity (f), FP area and FP perimeter (g) are extracted. (e) Schematic image of how SDL is measured. The length of the slit (in blue) is divided by the surface area (outlined in white) resulting in a length-density measurement of slit coverage. (f) Schematic image of how FP circularity is measured. From the segmentation of the individual foot processes, the FP circularity is calculated using the formula, circularity = 4 π (area/perimeter−2). The result is a value between 0 and 1 where a perfect circle has a circularity of 1 and a very elongated rectangle approaches 0. (g) Foot process size is calculated both by FP area and by FP perimeter. The FP area is the pixel area of each segmented foot process converted to µm 2 and the FP perimeter is the outline of the foot process with it closed at the base.

    Article Snippet: OCT-frozen biopsy specimens were fixed in PFA, cleared in 4% SDS w/ boric acid and fluorescently immunolabelled for nephrin (R&D Systems, cat. no. AF4269) to visualize the slit diaphragm and podocyte foot processes (FPs) based on the protocol described by Unnersjö-Jess et al (details available in Supplement Methods).

    Techniques: Imaging