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cd117  (R&D Systems)


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    R&D Systems cd117
    (A-B) H&E staining of primary TC tissue and corresponding 3DP organoids.Scale bars: 50 μm (C) Immunofluorescence images of TC organoids stained for DAPI, CD56, <t>CD117,</t> and pan-CK. Scale bars: 50 μm (D-E) H&E staining of primary THYM tissue and corresponding 3DP organoids. Scale bars: 50 μm (F) Immunofluorescence images of THYM organoids stained for DAPI, P63, pan-CK, and TdT.Scale bars: 100 μm. (G) CNV profiles of TC-Tumor. (H)TC-3DP organoids (I) TC-Matrigel organoids. (J) CNV profiles of THYM-Tumor. (K) THYM-3DP organoids. (L)THYM-Matrigel organoids.
    Cd117, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 183 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cd117/product/R&D Systems
    Average 94 stars, based on 183 article reviews
    cd117 - by Bioz Stars, 2026-04
    94/100 stars

    Images

    1) Product Images from "Biomimetic 3D-Bioprinted organoids of thymic epithelial tumors for translational drug screening and biomarker identification"

    Article Title: Biomimetic 3D-Bioprinted organoids of thymic epithelial tumors for translational drug screening and biomarker identification

    Journal: Materials Today Bio

    doi: 10.1016/j.mtbio.2026.102878

    (A-B) H&E staining of primary TC tissue and corresponding 3DP organoids.Scale bars: 50 μm (C) Immunofluorescence images of TC organoids stained for DAPI, CD56, CD117, and pan-CK. Scale bars: 50 μm (D-E) H&E staining of primary THYM tissue and corresponding 3DP organoids. Scale bars: 50 μm (F) Immunofluorescence images of THYM organoids stained for DAPI, P63, pan-CK, and TdT.Scale bars: 100 μm. (G) CNV profiles of TC-Tumor. (H)TC-3DP organoids (I) TC-Matrigel organoids. (J) CNV profiles of THYM-Tumor. (K) THYM-3DP organoids. (L)THYM-Matrigel organoids.
    Figure Legend Snippet: (A-B) H&E staining of primary TC tissue and corresponding 3DP organoids.Scale bars: 50 μm (C) Immunofluorescence images of TC organoids stained for DAPI, CD56, CD117, and pan-CK. Scale bars: 50 μm (D-E) H&E staining of primary THYM tissue and corresponding 3DP organoids. Scale bars: 50 μm (F) Immunofluorescence images of THYM organoids stained for DAPI, P63, pan-CK, and TdT.Scale bars: 100 μm. (G) CNV profiles of TC-Tumor. (H)TC-3DP organoids (I) TC-Matrigel organoids. (J) CNV profiles of THYM-Tumor. (K) THYM-3DP organoids. (L)THYM-Matrigel organoids.

    Techniques Used: Staining, Immunofluorescence



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    Image Search Results


    (A-B) H&E staining of primary TC tissue and corresponding 3DP organoids.Scale bars: 50 μm (C) Immunofluorescence images of TC organoids stained for DAPI, CD56, CD117, and pan-CK. Scale bars: 50 μm (D-E) H&E staining of primary THYM tissue and corresponding 3DP organoids. Scale bars: 50 μm (F) Immunofluorescence images of THYM organoids stained for DAPI, P63, pan-CK, and TdT.Scale bars: 100 μm. (G) CNV profiles of TC-Tumor. (H)TC-3DP organoids (I) TC-Matrigel organoids. (J) CNV profiles of THYM-Tumor. (K) THYM-3DP organoids. (L)THYM-Matrigel organoids.

    Journal: Materials Today Bio

    Article Title: Biomimetic 3D-Bioprinted organoids of thymic epithelial tumors for translational drug screening and biomarker identification

    doi: 10.1016/j.mtbio.2026.102878

    Figure Lengend Snippet: (A-B) H&E staining of primary TC tissue and corresponding 3DP organoids.Scale bars: 50 μm (C) Immunofluorescence images of TC organoids stained for DAPI, CD56, CD117, and pan-CK. Scale bars: 50 μm (D-E) H&E staining of primary THYM tissue and corresponding 3DP organoids. Scale bars: 50 μm (F) Immunofluorescence images of THYM organoids stained for DAPI, P63, pan-CK, and TdT.Scale bars: 100 μm. (G) CNV profiles of TC-Tumor. (H)TC-3DP organoids (I) TC-Matrigel organoids. (J) CNV profiles of THYM-Tumor. (K) THYM-3DP organoids. (L)THYM-Matrigel organoids.

    Article Snippet: The following primary antibodies were used: Pan-CK (# MA513203 , invitrogen) at a dilution of 1:100, CD117 (AF1356-SP, R&D system) at a dilution of 1:100, CD56/NACM1 (#ab313779, abcam) at a dilution of 1:100, p63 (#ab124762, abcam) at a dilution of 1:100, TdT (#TB4932S, abmart) at a dilution of 1:100, and Anti-gamma H2A.X (phospho S139) antibody (#ab2893, abcam) at a dilution of 1:100.

    Techniques: Staining, Immunofluorescence

    ACK2 antibody clearance from circulation and depletion of BM HSPCs. (A) Experimental design: C57BL/6 mice were injected i.p. with PBS or 500 μg of purified ACK2 antibody and peripheral blood was collected at days 3, 4, and 5 post-injection for the detection of ACK2 antibody in serum. Representative dot plots showing competition of serum-ACK2 with fluorescently labeled anti-c-Kit clone ACK2 for binding to Lin – c-Kit + BM cells, and corresponding boxplots showing median cell percentages and IQR with whiskers representing the lowest and highest values. (B) Experimental design: C57BL/6 mice were injected i.p. with PBS or 500 μg of purified ACK2 antibody and BM was collected at days 3, 4, and 5 post-injection for the detection of BM HSPCs. Representative dot plots showing Lin – c-Kit + cells labeled with anti-c-Kit clones 2B8 or 3C11 in PBS- and ACK2-injected mice, with boxplots showing median cell percentages and IQR with whiskers representing the lowest and highest values. Statistical significance was determined by non-parametric Kruskal-Wallis test with Dunn’s post hoc multiple comparisons (* P < 0.05; ** P < 0.01; *** P < 0.001). Dot plots shown are representative of individual samples. Data is a pool of two independent experiments from two independent ACK2 production batches. n = 3–8 mice per condition. Figure partially created in BioRender.com . Guiu, (A) (2026).

    Journal: Frontiers in Immunology

    Article Title: ACK2 antibody conditioning enhances adoptive transfer of hematopoietic progenitors to study central trained immunity in mice

    doi: 10.3389/fimmu.2026.1735878

    Figure Lengend Snippet: ACK2 antibody clearance from circulation and depletion of BM HSPCs. (A) Experimental design: C57BL/6 mice were injected i.p. with PBS or 500 μg of purified ACK2 antibody and peripheral blood was collected at days 3, 4, and 5 post-injection for the detection of ACK2 antibody in serum. Representative dot plots showing competition of serum-ACK2 with fluorescently labeled anti-c-Kit clone ACK2 for binding to Lin – c-Kit + BM cells, and corresponding boxplots showing median cell percentages and IQR with whiskers representing the lowest and highest values. (B) Experimental design: C57BL/6 mice were injected i.p. with PBS or 500 μg of purified ACK2 antibody and BM was collected at days 3, 4, and 5 post-injection for the detection of BM HSPCs. Representative dot plots showing Lin – c-Kit + cells labeled with anti-c-Kit clones 2B8 or 3C11 in PBS- and ACK2-injected mice, with boxplots showing median cell percentages and IQR with whiskers representing the lowest and highest values. Statistical significance was determined by non-parametric Kruskal-Wallis test with Dunn’s post hoc multiple comparisons (* P < 0.05; ** P < 0.01; *** P < 0.001). Dot plots shown are representative of individual samples. Data is a pool of two independent experiments from two independent ACK2 production batches. n = 3–8 mice per condition. Figure partially created in BioRender.com . Guiu, (A) (2026).

    Article Snippet: c-Kit (CD117) , PE-Vio770 , 3C11 , 1:50 , Miltenyi Biotec , 130-125-226.

    Techniques: Injection, Purification, Labeling, Binding Assay, Clone Assay