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Miltenyi Biotec cd117 pe
Cd117 Pe, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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(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.
Af1356, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems anti ckit
(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.
Anti Ckit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluidigm 3143001b
(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.
3143001b, supplied by fluidigm, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Novus Biologicals ckit
(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.
Ckit, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Miltenyi Biotec mouse cd117 conjugated microbeads
(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.
Mouse Cd117 Conjugated Microbeads, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Miltenyi Biotec 3c11
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 <t>3C11</t> 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).
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Bio X Cell anti mouse cd117 mabs
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 <t>3C11</t> 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).
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Miltenyi Biotec magnetic microbeads conjugated to c kit antibodies
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 <t>3C11</t> 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).
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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