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kidney tissue sections  (R&D Systems)


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    Structured Review

    R&D Systems kidney tissue sections
    Kidney Tissue Sections, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 296 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/kidney+tissue+sections/Mouse+TIM-1%2FKIM-1%2FHAVCR+Antibody/pmc11116430-258-16-24
    Average 96 stars, based on 296 article reviews
    kidney tissue sections - by Bioz Stars, 2026-09
    96/100 stars

    Images

    Related Articles

    Immunohistochemical staining:

    Article Title: Autophagy-deficient macrophages exacerbate cisplatin-induced mitochondrial dysfunction and kidney injury via miR-195a-5p-SIRT3 axis
    Article Snippet: .. For immunohistochemical staining, after quenching with endogenous peroxidase, antigen retrieval, and blocking nonspecific binding sites, the kidney tissue sections were incubated with anti-KIM1 (AF1817; RD Systems, Canada), anti-TNF-α (ab215188; Abcam, Cambridge, UK), and anti-ATP5b (A5769; ABlonal; Wuhan, China) overnight at 4 °C, followed by staining with horseradish peroxidase (HRP)-conjugated secondary antibodies (ABclonal) and 3,3′-diaminobenzidine (DAB) substrates. .. Images of stained sections were captured by a light microscope (Zeiss, AX10 imager A2, Oberkochen, Germany) and quantified by ImageJ software.

    Staining:

    Article Title: Autophagy-deficient macrophages exacerbate cisplatin-induced mitochondrial dysfunction and kidney injury via miR-195a-5p-SIRT3 axis
    Article Snippet: .. For immunohistochemical staining, after quenching with endogenous peroxidase, antigen retrieval, and blocking nonspecific binding sites, the kidney tissue sections were incubated with anti-KIM1 (AF1817; RD Systems, Canada), anti-TNF-α (ab215188; Abcam, Cambridge, UK), and anti-ATP5b (A5769; ABlonal; Wuhan, China) overnight at 4 °C, followed by staining with horseradish peroxidase (HRP)-conjugated secondary antibodies (ABclonal) and 3,3′-diaminobenzidine (DAB) substrates. .. Images of stained sections were captured by a light microscope (Zeiss, AX10 imager A2, Oberkochen, Germany) and quantified by ImageJ software.

    Blocking Assay:

    Article Title: Autophagy-deficient macrophages exacerbate cisplatin-induced mitochondrial dysfunction and kidney injury via miR-195a-5p-SIRT3 axis
    Article Snippet: .. For immunohistochemical staining, after quenching with endogenous peroxidase, antigen retrieval, and blocking nonspecific binding sites, the kidney tissue sections were incubated with anti-KIM1 (AF1817; RD Systems, Canada), anti-TNF-α (ab215188; Abcam, Cambridge, UK), and anti-ATP5b (A5769; ABlonal; Wuhan, China) overnight at 4 °C, followed by staining with horseradish peroxidase (HRP)-conjugated secondary antibodies (ABclonal) and 3,3′-diaminobenzidine (DAB) substrates. .. Images of stained sections were captured by a light microscope (Zeiss, AX10 imager A2, Oberkochen, Germany) and quantified by ImageJ software.

    Binding Assay:

    Article Title: Autophagy-deficient macrophages exacerbate cisplatin-induced mitochondrial dysfunction and kidney injury via miR-195a-5p-SIRT3 axis
    Article Snippet: .. For immunohistochemical staining, after quenching with endogenous peroxidase, antigen retrieval, and blocking nonspecific binding sites, the kidney tissue sections were incubated with anti-KIM1 (AF1817; RD Systems, Canada), anti-TNF-α (ab215188; Abcam, Cambridge, UK), and anti-ATP5b (A5769; ABlonal; Wuhan, China) overnight at 4 °C, followed by staining with horseradish peroxidase (HRP)-conjugated secondary antibodies (ABclonal) and 3,3′-diaminobenzidine (DAB) substrates. .. Images of stained sections were captured by a light microscope (Zeiss, AX10 imager A2, Oberkochen, Germany) and quantified by ImageJ software.

    Incubation:

    Article Title: Autophagy-deficient macrophages exacerbate cisplatin-induced mitochondrial dysfunction and kidney injury via miR-195a-5p-SIRT3 axis
    Article Snippet: .. For immunohistochemical staining, after quenching with endogenous peroxidase, antigen retrieval, and blocking nonspecific binding sites, the kidney tissue sections were incubated with anti-KIM1 (AF1817; RD Systems, Canada), anti-TNF-α (ab215188; Abcam, Cambridge, UK), and anti-ATP5b (A5769; ABlonal; Wuhan, China) overnight at 4 °C, followed by staining with horseradish peroxidase (HRP)-conjugated secondary antibodies (ABclonal) and 3,3′-diaminobenzidine (DAB) substrates. .. Images of stained sections were captured by a light microscope (Zeiss, AX10 imager A2, Oberkochen, Germany) and quantified by ImageJ software.



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    R&D Systems kidney tissue sections
    a Timeline of AKI modeling and treatment with mice. CRE ( b ) and BUN ( c ) levels in the blood serum from each group after indicated treatments ( n = 3; Data are presented as means ± SD. * P < 0.1, n.s. no significance. P values in ( b ): 2.0 × 10 – 2 , 2.1 × 10 – 2 , 1.8 × 10 – 1 and 2.3 × 10 – 2 , P values in ( c ): 3.4 × 10 – 2 , 2.9 × 10 – 2 , 2.6 × 10 – 1 and 5.6 × 10 – 2 ). d The survival rate of AKI mice treated with PBS and MF-0, respectively. e H&E <t>staining</t> of renal sections from each treatment group. Arrows indicated damaged tubules and asterisks indicated the formation of casts (a marker of more severe tubular damage). f DAPI (blue fluorescence indicating cell nuclei) and dihydroethidium (red fluorescence indicating ROS level) staining of <t>kidney</t> <t>tissues</t> from each treatment group. NAC used in ( b , c , e , f ) was a ROS inhibitor. The injection dosage of agents in different treatment groups was 200 μL: NAC (800 μg/mL), MF-0 (800 μg of Mo per mL). Significance was calculated by one-sided Student’s t -test. Source data are provided as a Source Data file.
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    a Timeline of AKI modeling and treatment with mice. CRE ( b ) and BUN ( c ) levels in the blood serum from each group after indicated treatments ( n = 3; Data are presented as means ± SD. * P < 0.1, n.s. no significance. P values in ( b ): 2.0 × 10 – 2 , 2.1 × 10 – 2 , 1.8 × 10 – 1 and 2.3 × 10 – 2 , P values in ( c ): 3.4 × 10 – 2 , 2.9 × 10 – 2 , 2.6 × 10 – 1 and 5.6 × 10 – 2 ). d The survival rate of AKI mice treated with PBS and MF-0, respectively. e H&E <t>staining</t> of renal sections from each treatment group. Arrows indicated damaged tubules and asterisks indicated the formation of casts (a marker of more severe tubular damage). f DAPI (blue fluorescence indicating cell nuclei) and dihydroethidium (red fluorescence indicating ROS level) staining of <t>kidney</t> <t>tissues</t> from each treatment group. NAC used in ( b , c , e , f ) was a ROS inhibitor. The injection dosage of agents in different treatment groups was 200 μL: NAC (800 μg/mL), MF-0 (800 μg of Mo per mL). Significance was calculated by one-sided Student’s t -test. Source data are provided as a Source Data file.
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    Proteintech human kidney tissue sections
    a Timeline of AKI modeling and treatment with mice. CRE ( b ) and BUN ( c ) levels in the blood serum from each group after indicated treatments ( n = 3; Data are presented as means ± SD. * P < 0.1, n.s. no significance. P values in ( b ): 2.0 × 10 – 2 , 2.1 × 10 – 2 , 1.8 × 10 – 1 and 2.3 × 10 – 2 , P values in ( c ): 3.4 × 10 – 2 , 2.9 × 10 – 2 , 2.6 × 10 – 1 and 5.6 × 10 – 2 ). d The survival rate of AKI mice treated with PBS and MF-0, respectively. e H&E <t>staining</t> of renal sections from each treatment group. Arrows indicated damaged tubules and asterisks indicated the formation of casts (a marker of more severe tubular damage). f DAPI (blue fluorescence indicating cell nuclei) and dihydroethidium (red fluorescence indicating ROS level) staining of <t>kidney</t> <t>tissues</t> from each treatment group. NAC used in ( b , c , e , f ) was a ROS inhibitor. The injection dosage of agents in different treatment groups was 200 μL: NAC (800 μg/mL), MF-0 (800 μg of Mo per mL). Significance was calculated by one-sided Student’s t -test. Source data are provided as a Source Data file.
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    Image Search Results


    a Timeline of AKI modeling and treatment with mice. CRE ( b ) and BUN ( c ) levels in the blood serum from each group after indicated treatments ( n = 3; Data are presented as means ± SD. * P < 0.1, n.s. no significance. P values in ( b ): 2.0 × 10 – 2 , 2.1 × 10 – 2 , 1.8 × 10 – 1 and 2.3 × 10 – 2 , P values in ( c ): 3.4 × 10 – 2 , 2.9 × 10 – 2 , 2.6 × 10 – 1 and 5.6 × 10 – 2 ). d The survival rate of AKI mice treated with PBS and MF-0, respectively. e H&E staining of renal sections from each treatment group. Arrows indicated damaged tubules and asterisks indicated the formation of casts (a marker of more severe tubular damage). f DAPI (blue fluorescence indicating cell nuclei) and dihydroethidium (red fluorescence indicating ROS level) staining of kidney tissues from each treatment group. NAC used in ( b , c , e , f ) was a ROS inhibitor. The injection dosage of agents in different treatment groups was 200 μL: NAC (800 μg/mL), MF-0 (800 μg of Mo per mL). Significance was calculated by one-sided Student’s t -test. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Valence-engineered catalysis-selectivity regulation of molybdenum oxide nanozyme for acute kidney injury therapy and post-cure assessment

    doi: 10.1038/s41467-024-53047-1

    Figure Lengend Snippet: a Timeline of AKI modeling and treatment with mice. CRE ( b ) and BUN ( c ) levels in the blood serum from each group after indicated treatments ( n = 3; Data are presented as means ± SD. * P < 0.1, n.s. no significance. P values in ( b ): 2.0 × 10 – 2 , 2.1 × 10 – 2 , 1.8 × 10 – 1 and 2.3 × 10 – 2 , P values in ( c ): 3.4 × 10 – 2 , 2.9 × 10 – 2 , 2.6 × 10 – 1 and 5.6 × 10 – 2 ). d The survival rate of AKI mice treated with PBS and MF-0, respectively. e H&E staining of renal sections from each treatment group. Arrows indicated damaged tubules and asterisks indicated the formation of casts (a marker of more severe tubular damage). f DAPI (blue fluorescence indicating cell nuclei) and dihydroethidium (red fluorescence indicating ROS level) staining of kidney tissues from each treatment group. NAC used in ( b , c , e , f ) was a ROS inhibitor. The injection dosage of agents in different treatment groups was 200 μL: NAC (800 μg/mL), MF-0 (800 μg of Mo per mL). Significance was calculated by one-sided Student’s t -test. Source data are provided as a Source Data file.

    Article Snippet: Photographs of cell imaging and kidney tissue section staining were obtained using a model eclipse Ti2-U inverted fluorescence microscope (Nikon).

    Techniques: Staining, Marker, Fluorescence, Injection