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kidney tissue sections  (Proteintech)


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    Structured Review

    Proteintech kidney tissue sections
    Kidney Tissue Sections, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/kidney+tissue+sections/ACSF2+Antibody/pm38676722-59-4-13
    Average 93 stars, based on 11 article reviews
    kidney tissue sections - by Bioz Stars, 2026-10
    93/100 stars

    Images

    Related Articles

    Immunohistochemical staining:

    Article Title: ACSF2 and lysine lactylation contribute to renal tubule injury in diabetes.
    Article Snippet: Aims Lactate accumulation is reported to be a biomarker for diabetic nephropathy progression.. Lactate drives lysine lactylation, a newly discovered post-translational modification that is involved in the pathogenesis of cancers and metabolic and inflammatory disease.. Here, we aimed to determine whether lysine lactylation is involved in the pathogenesis of diabetic nephropathy.

    Immunohistochemistry:

    Article Title: ACSF2 and lysine lactylation contribute to renal tubule injury in diabetes.
    Article Snippet: Aims Lactate accumulation is reported to be a biomarker for diabetic nephropathy progression.. Lactate drives lysine lactylation, a newly discovered post-translational modification that is involved in the pathogenesis of cancers and metabolic and inflammatory disease.. Here, we aimed to determine whether lysine lactylation is involved in the pathogenesis of diabetic nephropathy.

    Article Title: Proteomic analysis of mitochondria associated membranes in renal ischemic reperfusion injury
    Article Snippet: .. For the IHC analysis, the kidney tissue sections were incubated with specific antibodies as follows: MFN2 polyclonal antibody (1:200,12186-1-AP, Proteintech, China) and BNIP3 monoclonal antibody (1:200,68091-1-Ig,Protintech,China). ..

    Staining:

    Article Title: ACSF2 and lysine lactylation contribute to renal tubule injury in diabetes.
    Article Snippet: Aims Lactate accumulation is reported to be a biomarker for diabetic nephropathy progression.. Lactate drives lysine lactylation, a newly discovered post-translational modification that is involved in the pathogenesis of cancers and metabolic and inflammatory disease.. Here, we aimed to determine whether lysine lactylation is involved in the pathogenesis of diabetic nephropathy.

    Incubation:

    Article Title: ACSF2 and lysine lactylation contribute to renal tubule injury in diabetes.
    Article Snippet: Aims Lactate accumulation is reported to be a biomarker for diabetic nephropathy progression.. Lactate drives lysine lactylation, a newly discovered post-translational modification that is involved in the pathogenesis of cancers and metabolic and inflammatory disease.. Here, we aimed to determine whether lysine lactylation is involved in the pathogenesis of diabetic nephropathy.

    Article Title: Mannan-binding lectin ameliorates renal fibrosis by suppressing macrophage-to-myofibroblast transition
    Article Snippet: .. The tissue slides were placed in an antigen retrieval unit with pH 8.0 EDTA, then incubated in 10 % normal goat serum for 1 h. Kidney tissue sections were incubated with primary antibody (α-SMA polyclonal antibody, 14395-1-AP, proteintech) at 4 °C for overnight and then incubated with secondary antibody (CoraLite488-conjugated Goat Anti-Rabbit IgG(H + L), SA00013-2; proteintech). ..

    Article Title: Proteomic analysis of mitochondria associated membranes in renal ischemic reperfusion injury
    Article Snippet: .. For the IHC analysis, the kidney tissue sections were incubated with specific antibodies as follows: MFN2 polyclonal antibody (1:200,12186-1-AP, Proteintech, China) and BNIP3 monoclonal antibody (1:200,68091-1-Ig,Protintech,China). ..

    Blocking Assay:

    Article Title: ACSF2 and lysine lactylation contribute to renal tubule injury in diabetes.
    Article Snippet: Aims Lactate accumulation is reported to be a biomarker for diabetic nephropathy progression.. Lactate drives lysine lactylation, a newly discovered post-translational modification that is involved in the pathogenesis of cancers and metabolic and inflammatory disease.. Here, we aimed to determine whether lysine lactylation is involved in the pathogenesis of diabetic nephropathy.



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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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    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