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mouse anti kim 1 antibody  (R&D Systems)


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    Structured Review

    R&D Systems mouse anti kim 1 antibody
    Mouse Anti Kim 1 Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 99/100, based on 74 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti kim 1 antibody/product/R&D Systems
    Average 99 stars, based on 74 article reviews
    mouse anti kim 1 antibody - by Bioz Stars, 2026-04
    99/100 stars

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    Characterization of altered proximal tubule cells (A) UMAP representation of the PT compartment from AKI and control patients. (B) Relative abundance of PT1 and PT2 clusters in AKI and control patients. (C) Expression of known injury marker genes in PT1 and PT2 clusters. (D and E) Gene-weighted density of <t>HAVCR1</t> and VCAM1. (F) Enrichment score calculated by gene set enrichment analysis using Reactome pathway database (positive enrichment means an enrichment in PT2 cluster). (G) Pathway activity in PT1 and PT2 clusters (inferred from PROGENy). (H) Collagen, extracellular matrix (ecm) proteoglycan (pg) and glycoprotein (gp) scores in PT1 and PT2 clusters. (I) Potential of heat-diffusion for affinity-based trajectory embedding (PHATE) dimension reduction projecting pathway enrichment estimated by GSVA for each cell type. (J and K) Representative immunostainings of HAVCR1 (J) and VCAM-1 (K) proteins in fibrotic area. ∗∗∗p < 0.001 ∗∗∗∗p < 0.0001.
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    Characterization of altered proximal tubule cells (A) UMAP representation of the PT compartment from AKI and control patients. (B) Relative abundance of PT1 and PT2 clusters in AKI and control patients. (C) Expression of known injury marker genes in PT1 and PT2 clusters. (D and E) Gene-weighted density of <t>HAVCR1</t> and VCAM1. (F) Enrichment score calculated by gene set enrichment analysis using Reactome pathway database (positive enrichment means an enrichment in PT2 cluster). (G) Pathway activity in PT1 and PT2 clusters (inferred from PROGENy). (H) Collagen, extracellular matrix (ecm) proteoglycan (pg) and glycoprotein (gp) scores in PT1 and PT2 clusters. (I) Potential of heat-diffusion for affinity-based trajectory embedding (PHATE) dimension reduction projecting pathway enrichment estimated by GSVA for each cell type. (J and K) Representative immunostainings of HAVCR1 (J) and VCAM-1 (K) proteins in fibrotic area. ∗∗∗p < 0.001 ∗∗∗∗p < 0.0001.
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    Image Search Results


    Journal: Cell Reports Medicine

    Article Title: Chimeric antigen receptor-induced antigen loss protects CD5.CART cells from fratricide without compromising on-target cytotoxicity

    doi: 10.1016/j.xcrm.2024.101628

    Figure Lengend Snippet:

    Article Snippet: Mouse anti-human CD366 (TIM-3) BV421 (clone 7D3) , BD Biosciences , Cat#565562; RRID: AB_2744369.

    Techniques: Enzyme-linked Immunosorbent Assay, Antibody Labeling, Western Blot, Sequencing, CRISPR, Software

    Journal: Cell Reports Methods

    Article Title: An autologous ex vivo model for exploring patient-specific responses to viro-immunotherapy in glioblastoma

    doi: 10.1016/j.crmeth.2024.100716

    Figure Lengend Snippet:

    Article Snippet: Viobright FITC conjugated mouse anti-human Tim-3 , Miltenyi Biotec , Cat#130-126-004; clone F38-2E2; RRID: AB_2889789.

    Techniques: Staining, Virus, Recombinant, Gene Expression, Enzyme-linked Immunosorbent Assay, Cell Viability Assay, Software

    Characterization of altered proximal tubule cells (A) UMAP representation of the PT compartment from AKI and control patients. (B) Relative abundance of PT1 and PT2 clusters in AKI and control patients. (C) Expression of known injury marker genes in PT1 and PT2 clusters. (D and E) Gene-weighted density of HAVCR1 and VCAM1. (F) Enrichment score calculated by gene set enrichment analysis using Reactome pathway database (positive enrichment means an enrichment in PT2 cluster). (G) Pathway activity in PT1 and PT2 clusters (inferred from PROGENy). (H) Collagen, extracellular matrix (ecm) proteoglycan (pg) and glycoprotein (gp) scores in PT1 and PT2 clusters. (I) Potential of heat-diffusion for affinity-based trajectory embedding (PHATE) dimension reduction projecting pathway enrichment estimated by GSVA for each cell type. (J and K) Representative immunostainings of HAVCR1 (J) and VCAM-1 (K) proteins in fibrotic area. ∗∗∗p < 0.001 ∗∗∗∗p < 0.0001.

    Journal: iScience

    Article Title: A transfer learning framework to elucidate the clinical relevance of altered proximal tubule cell states in kidney disease

    doi: 10.1016/j.isci.2024.109271

    Figure Lengend Snippet: Characterization of altered proximal tubule cells (A) UMAP representation of the PT compartment from AKI and control patients. (B) Relative abundance of PT1 and PT2 clusters in AKI and control patients. (C) Expression of known injury marker genes in PT1 and PT2 clusters. (D and E) Gene-weighted density of HAVCR1 and VCAM1. (F) Enrichment score calculated by gene set enrichment analysis using Reactome pathway database (positive enrichment means an enrichment in PT2 cluster). (G) Pathway activity in PT1 and PT2 clusters (inferred from PROGENy). (H) Collagen, extracellular matrix (ecm) proteoglycan (pg) and glycoprotein (gp) scores in PT1 and PT2 clusters. (I) Potential of heat-diffusion for affinity-based trajectory embedding (PHATE) dimension reduction projecting pathway enrichment estimated by GSVA for each cell type. (J and K) Representative immunostainings of HAVCR1 (J) and VCAM-1 (K) proteins in fibrotic area. ∗∗∗p < 0.001 ∗∗∗∗p < 0.0001.

    Article Snippet: mouse monoclonal anti-human HAVCR1 , clone 219211 , MAB1750; RRID: AB_2116559 ; RD Systems.

    Techniques: Control, Expressing, Marker, Activity Assay, Diffusion-based Assay

    Journal: iScience

    Article Title: A transfer learning framework to elucidate the clinical relevance of altered proximal tubule cell states in kidney disease

    doi: 10.1016/j.isci.2024.109271

    Figure Lengend Snippet:

    Article Snippet: mouse monoclonal anti-human HAVCR1 , clone 219211 , MAB1750; RRID: AB_2116559 ; RD Systems.

    Techniques: Control, Software

    Characterization of altered proximal tubule cells (A) UMAP representation of the PT compartment from AKI and control patients. (B) Relative abundance of PT1 and PT2 clusters in AKI and control patients. (C) Expression of known injury marker genes in PT1 and PT2 clusters. (D and E) Gene-weighted density of HAVCR1 and VCAM1. (F) Enrichment score calculated by gene set enrichment analysis using Reactome pathway database (positive enrichment means an enrichment in PT2 cluster). (G) Pathway activity in PT1 and PT2 clusters (inferred from PROGENy). (H) Collagen, extracellular matrix (ecm) proteoglycan (pg) and glycoprotein (gp) scores in PT1 and PT2 clusters. (I) Potential of heat-diffusion for affinity-based trajectory embedding (PHATE) dimension reduction projecting pathway enrichment estimated by GSVA for each cell type. (J and K) Representative immunostainings of HAVCR1 (J) and VCAM-1 (K) proteins in fibrotic area. ∗∗∗p < 0.001 ∗∗∗∗p < 0.0001.

    Journal: iScience

    Article Title: A transfer learning framework to elucidate the clinical relevance of altered proximal tubule cell states in kidney disease

    doi: 10.1016/j.isci.2024.109271

    Figure Lengend Snippet: Characterization of altered proximal tubule cells (A) UMAP representation of the PT compartment from AKI and control patients. (B) Relative abundance of PT1 and PT2 clusters in AKI and control patients. (C) Expression of known injury marker genes in PT1 and PT2 clusters. (D and E) Gene-weighted density of HAVCR1 and VCAM1. (F) Enrichment score calculated by gene set enrichment analysis using Reactome pathway database (positive enrichment means an enrichment in PT2 cluster). (G) Pathway activity in PT1 and PT2 clusters (inferred from PROGENy). (H) Collagen, extracellular matrix (ecm) proteoglycan (pg) and glycoprotein (gp) scores in PT1 and PT2 clusters. (I) Potential of heat-diffusion for affinity-based trajectory embedding (PHATE) dimension reduction projecting pathway enrichment estimated by GSVA for each cell type. (J and K) Representative immunostainings of HAVCR1 (J) and VCAM-1 (K) proteins in fibrotic area. ∗∗∗p < 0.001 ∗∗∗∗p < 0.0001.

    Article Snippet: Immunochemistry staining were performed as followed: after antigen retrieval with pressurized heating chamber in citrate buffer pH7 or tris-EDTA pH9, 5μm tissue sections were incubated with antibodies mouse monoclonal anti-human HAVCR1 (dilution 1:250, clone 219211, RD Systems) and mouse monoclonal anti-human VCAM1 (dilution 1:25, clone 1.4C3, Invitrogen) for 1h at room temperature.

    Techniques: Control, Expressing, Marker, Activity Assay, Diffusion-based Assay

    Journal: iScience

    Article Title: A transfer learning framework to elucidate the clinical relevance of altered proximal tubule cell states in kidney disease

    doi: 10.1016/j.isci.2024.109271

    Figure Lengend Snippet:

    Article Snippet: Immunochemistry staining were performed as followed: after antigen retrieval with pressurized heating chamber in citrate buffer pH7 or tris-EDTA pH9, 5μm tissue sections were incubated with antibodies mouse monoclonal anti-human HAVCR1 (dilution 1:250, clone 219211, RD Systems) and mouse monoclonal anti-human VCAM1 (dilution 1:25, clone 1.4C3, Invitrogen) for 1h at room temperature.

    Techniques: Control, Software