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Thermo Fisher pe-cyanine5 cd135 (flt3) monoclonal antibody (a2f10)
Cleavage under targets and tagmentation sequencing of IRF4 binding in intestinal ILC3 subsets (A) Heatmap showing the genome-wide distribution of IRF4-binding signals at peak centers in ILC3 subsets sorted from Irf4 f/f and Irf4 f/f Rorc cre mice by CUT&Tag. (B) Occupancy of IRF4 at all gene promoter regions (±5 kb of TSS). (C) Donut chart showing the percentages of IRF4 binding at exon regions, intron regions, or intergenic regions. (D) Venn plot displaying the overlap of the IRF4-regulated genes from pairwise comparisons of NKp46 + ILC3s, NKp46 − CCR6 − ILC3s, and CCR6 + ILC3s. (E) Gene set enrichment analysis (GSEA) of NKp46 + ILC3 signature gene sets enriched in shared IRF4-modified genes. (F and G) IGV visualizes the indicated gene locus containing ATAC-seq and IRF4-binding peaks in ILC3 subsets. IRF4 CUT&Tag sequencing data are from two independent replicates. (H–K) Rescue experiments. Retroviruses were generated by transfection of pMX-IRES-GFP plasmids containing the indicated genes into Plat-E cells using PolyJet. CLPs (Lin − CD127 + c-Kit int Sca-1 int <t>Flt3</t> + ) were sorted from the bone marrow from Irf4 f/f and Irf4f/f Rorc cre mice and transfected with retroviral supernatants. Retrovirus-transfected CLPs were then collected and adoptively transferred into sublethally irradiated CD45.1 + wild-type recipient mice through intravenous tail vein injection. Transduced cells were transferred with CD45.1 + wild-type bone marrow cells to help the engraftment of the CLPs. After 2 weeks, recipient mice were sacrificed, and organs were collected for analysis. (H) Flow cytometry of CD45.2 + GFP + ILC3 subsets isolated from the siLP in the indicated recipient mice (upper). MHC class II expression of CD45.2 + GFP + ILC3 subsets isolated from the siLP in the indicated recipient mice (lower). (I) Cytokine production in siLP CD45.2 + GFP + ILC3s from the indicated recipient mice. (J) The percentages of the indicated subsets were compared. (K) The percentages of MHC class II + ILC3s, IL-17A + ILC3s, and IL-22 + ILC3s were compared. Bar graphs are presented as mean ± SEM. A two-tailed Student’s t test was performed for comparisons. The data are representative of at least three independent experiments. See also .
Pe Cyanine5 Cd135 (Flt3) Monoclonal Antibody (A2f10), supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cd135+a2f10/pmc12205599-33-0-7?v=Thermo+Fisher
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pe-cyanine5 cd135 (flt3) monoclonal antibody (a2f10) - by Bioz Stars, 2026-07
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Thermo Fisher cd135 a2f10
Cleavage under targets and tagmentation sequencing of IRF4 binding in intestinal ILC3 subsets (A) Heatmap showing the genome-wide distribution of IRF4-binding signals at peak centers in ILC3 subsets sorted from Irf4 f/f and Irf4 f/f Rorc cre mice by CUT&Tag. (B) Occupancy of IRF4 at all gene promoter regions (±5 kb of TSS). (C) Donut chart showing the percentages of IRF4 binding at exon regions, intron regions, or intergenic regions. (D) Venn plot displaying the overlap of the IRF4-regulated genes from pairwise comparisons of NKp46 + ILC3s, NKp46 − CCR6 − ILC3s, and CCR6 + ILC3s. (E) Gene set enrichment analysis (GSEA) of NKp46 + ILC3 signature gene sets enriched in shared IRF4-modified genes. (F and G) IGV visualizes the indicated gene locus containing ATAC-seq and IRF4-binding peaks in ILC3 subsets. IRF4 CUT&Tag sequencing data are from two independent replicates. (H–K) Rescue experiments. Retroviruses were generated by transfection of pMX-IRES-GFP plasmids containing the indicated genes into Plat-E cells using PolyJet. CLPs (Lin − CD127 + c-Kit int Sca-1 int <t>Flt3</t> + ) were sorted from the bone marrow from Irf4 f/f and Irf4f/f Rorc cre mice and transfected with retroviral supernatants. Retrovirus-transfected CLPs were then collected and adoptively transferred into sublethally irradiated CD45.1 + wild-type recipient mice through intravenous tail vein injection. Transduced cells were transferred with CD45.1 + wild-type bone marrow cells to help the engraftment of the CLPs. After 2 weeks, recipient mice were sacrificed, and organs were collected for analysis. (H) Flow cytometry of CD45.2 + GFP + ILC3 subsets isolated from the siLP in the indicated recipient mice (upper). MHC class II expression of CD45.2 + GFP + ILC3 subsets isolated from the siLP in the indicated recipient mice (lower). (I) Cytokine production in siLP CD45.2 + GFP + ILC3s from the indicated recipient mice. (J) The percentages of the indicated subsets were compared. (K) The percentages of MHC class II + ILC3s, IL-17A + ILC3s, and IL-22 + ILC3s were compared. Bar graphs are presented as mean ± SEM. A two-tailed Student’s t test was performed for comparisons. The data are representative of at least three independent experiments. See also .
Cd135 A2f10, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cd135+a2f10/bio_rxiv__2024__09__13__612924-91-14-22?v=Thermo+Fisher
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cd135 a2f10 - by Bioz Stars, 2026-07
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Thermo Fisher pe - cd135 (flt3) monoclonal antibody (a2f10)
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Pe Cd135 (Flt3) Monoclonal Antibody (A2f10), supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson anti-cd135 a2f10
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Dakewe Biotech Co pe-anti-mouse cd135 (flt3, catalogue number 135306; clone name, a2f10; 1:100)
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Pe Anti Mouse Cd135 (Flt3, Catalogue Number 135306; Clone Name, A2f10; 1:100), supplied by Dakewe Biotech Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher anti-cd135 (clone a2f10)

Anti Cd135 (Clone A2f10), supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher anti cd135 (clone a2f10)

Anti Cd135 (Clone A2f10), supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher flt3 (cd135) a2f10
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Flt3 (Cd135) A2f10, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher cd135 (flt3) percp-cy5.5 (a2f10) antibody
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Cd135 (Flt3) Percp Cy5.5 (A2f10) Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher cd135 (flt3) monoclonal antibody (a2f10), percp-efluor 710
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Cd135 (Flt3) Monoclonal Antibody (A2f10), Percp Efluor 710, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cleavage under targets and tagmentation sequencing of IRF4 binding in intestinal ILC3 subsets (A) Heatmap showing the genome-wide distribution of IRF4-binding signals at peak centers in ILC3 subsets sorted from Irf4 f/f and Irf4 f/f Rorc cre mice by CUT&Tag. (B) Occupancy of IRF4 at all gene promoter regions (±5 kb of TSS). (C) Donut chart showing the percentages of IRF4 binding at exon regions, intron regions, or intergenic regions. (D) Venn plot displaying the overlap of the IRF4-regulated genes from pairwise comparisons of NKp46 + ILC3s, NKp46 − CCR6 − ILC3s, and CCR6 + ILC3s. (E) Gene set enrichment analysis (GSEA) of NKp46 + ILC3 signature gene sets enriched in shared IRF4-modified genes. (F and G) IGV visualizes the indicated gene locus containing ATAC-seq and IRF4-binding peaks in ILC3 subsets. IRF4 CUT&Tag sequencing data are from two independent replicates. (H–K) Rescue experiments. Retroviruses were generated by transfection of pMX-IRES-GFP plasmids containing the indicated genes into Plat-E cells using PolyJet. CLPs (Lin − CD127 + c-Kit int Sca-1 int Flt3 + ) were sorted from the bone marrow from Irf4 f/f and Irf4f/f Rorc cre mice and transfected with retroviral supernatants. Retrovirus-transfected CLPs were then collected and adoptively transferred into sublethally irradiated CD45.1 + wild-type recipient mice through intravenous tail vein injection. Transduced cells were transferred with CD45.1 + wild-type bone marrow cells to help the engraftment of the CLPs. After 2 weeks, recipient mice were sacrificed, and organs were collected for analysis. (H) Flow cytometry of CD45.2 + GFP + ILC3 subsets isolated from the siLP in the indicated recipient mice (upper). MHC class II expression of CD45.2 + GFP + ILC3 subsets isolated from the siLP in the indicated recipient mice (lower). (I) Cytokine production in siLP CD45.2 + GFP + ILC3s from the indicated recipient mice. (J) The percentages of the indicated subsets were compared. (K) The percentages of MHC class II + ILC3s, IL-17A + ILC3s, and IL-22 + ILC3s were compared. Bar graphs are presented as mean ± SEM. A two-tailed Student’s t test was performed for comparisons. The data are representative of at least three independent experiments. See also .

Journal: iScience

Article Title: The transcription factor IRF4 regulates the homeostasis and function of intestinal ILC3s

doi: 10.1016/j.isci.2025.112800

Figure Lengend Snippet: Cleavage under targets and tagmentation sequencing of IRF4 binding in intestinal ILC3 subsets (A) Heatmap showing the genome-wide distribution of IRF4-binding signals at peak centers in ILC3 subsets sorted from Irf4 f/f and Irf4 f/f Rorc cre mice by CUT&Tag. (B) Occupancy of IRF4 at all gene promoter regions (±5 kb of TSS). (C) Donut chart showing the percentages of IRF4 binding at exon regions, intron regions, or intergenic regions. (D) Venn plot displaying the overlap of the IRF4-regulated genes from pairwise comparisons of NKp46 + ILC3s, NKp46 − CCR6 − ILC3s, and CCR6 + ILC3s. (E) Gene set enrichment analysis (GSEA) of NKp46 + ILC3 signature gene sets enriched in shared IRF4-modified genes. (F and G) IGV visualizes the indicated gene locus containing ATAC-seq and IRF4-binding peaks in ILC3 subsets. IRF4 CUT&Tag sequencing data are from two independent replicates. (H–K) Rescue experiments. Retroviruses were generated by transfection of pMX-IRES-GFP plasmids containing the indicated genes into Plat-E cells using PolyJet. CLPs (Lin − CD127 + c-Kit int Sca-1 int Flt3 + ) were sorted from the bone marrow from Irf4 f/f and Irf4f/f Rorc cre mice and transfected with retroviral supernatants. Retrovirus-transfected CLPs were then collected and adoptively transferred into sublethally irradiated CD45.1 + wild-type recipient mice through intravenous tail vein injection. Transduced cells were transferred with CD45.1 + wild-type bone marrow cells to help the engraftment of the CLPs. After 2 weeks, recipient mice were sacrificed, and organs were collected for analysis. (H) Flow cytometry of CD45.2 + GFP + ILC3 subsets isolated from the siLP in the indicated recipient mice (upper). MHC class II expression of CD45.2 + GFP + ILC3 subsets isolated from the siLP in the indicated recipient mice (lower). (I) Cytokine production in siLP CD45.2 + GFP + ILC3s from the indicated recipient mice. (J) The percentages of the indicated subsets were compared. (K) The percentages of MHC class II + ILC3s, IL-17A + ILC3s, and IL-22 + ILC3s were compared. Bar graphs are presented as mean ± SEM. A two-tailed Student’s t test was performed for comparisons. The data are representative of at least three independent experiments. See also .

Article Snippet: PE-Cyanine5 CD135 (Flt3) Monoclonal Antibody (A2F10) , eBioscience , Cat# 15-1351-82; RRID: AB_494219.

Techniques: Sequencing, Binding Assay, Genome Wide, Modification, Generated, Transfection, Retroviral, Irradiation, Injection, Flow Cytometry, Isolation, Expressing, Two Tailed Test

KEY RESOURCES TABLE

Journal: Cell reports

Article Title: G2 arrest primes hematopoietic stem cells for megakaryopoiesis

doi: 10.1016/j.celrep.2024.114388

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: PE - CD135 (Flt3) Monoclonal Antibody (A2F10) , Thermo Fisher Scientific , Cat# 12-1351-82; RRID: AB_465859.

Techniques: Recombinant, Adhesive, Purification, Blocking Assay, Amplification, Random Hexamer, Reverse Transcription, SYBR Green Assay, Sterility, Imaging, Software

Journal: Cell Reports Medicine

Article Title: FLT3L-dependent dendritic cells control tumor immunity by modulating Treg and NK cell homeostasis

doi: 10.1016/j.xcrm.2023.101256

Figure Lengend Snippet:

Article Snippet: Anti-CD135 (clone A2F10) , eBioscience , Cat# 13-1351-85; RRID: AB_466600.

Techniques: Control, Recombinant, Staining, Cell Isolation, Software

Journal: Cell Reports Medicine

Article Title: FLT3L-dependent dendritic cells control tumor immunity by modulating Treg and NK cell homeostasis

doi: 10.1016/j.xcrm.2023.101256

Figure Lengend Snippet:

Article Snippet: Anti CD135 (clone A2F10) , eBioscience , Cat# 15-1351-82; RRID: AB_494219.

Techniques: Control, Recombinant, Staining, Cell Isolation, Software

Reagents.

Journal: eLife

Article Title: Regulation of pDC fate determination by histone deacetylase 3

doi: 10.7554/eLife.80477

Figure Lengend Snippet: Reagents.

Article Snippet: FLT3 (CD135) , A2F10 , eBioscience.

Techniques:

Reagents, antibodies, chemicals, and solutions

Journal: European journal of immunology

Article Title: Guidelines for mouse and human DC generation

doi: 10.1002/eji.202249816

Figure Lengend Snippet: Reagents, antibodies, chemicals, and solutions

Article Snippet: CD135 (Flt3) PerCP-Cy5.5 (A2F10) , eBioscience , 46-1351-82.

Techniques: Recombinant, Saline

Representative flow cytometry analysis of HoxB8 MPP differentiation into CDP and DC subsets. (A) HoxB8 MPP are cultured in HoxB8 growth medium without E2 for 3 days and analyzed by flow cytometry ( , step 5). MPP: Gr1 − CD117 + CD135 − ; CDP: Gr1 − CD117 int/low CD135 + CD115 + . (B) HoxB8 MPP are cultured in HoxB8 growth medium without E2 for 8 days and analyzed by flow cytometry (see below , step 7). cDC1: Gr1 − CD11c + CD11b low/− XCR1 + ; cDC2: Gr1 − CD11c + CD11b + XCR1 − ; pDC: Gr1 − CD11c + CD11b − B220 + .

Journal: European journal of immunology

Article Title: Guidelines for mouse and human DC generation

doi: 10.1002/eji.202249816

Figure Lengend Snippet: Representative flow cytometry analysis of HoxB8 MPP differentiation into CDP and DC subsets. (A) HoxB8 MPP are cultured in HoxB8 growth medium without E2 for 3 days and analyzed by flow cytometry ( , step 5). MPP: Gr1 − CD117 + CD135 − ; CDP: Gr1 − CD117 int/low CD135 + CD115 + . (B) HoxB8 MPP are cultured in HoxB8 growth medium without E2 for 8 days and analyzed by flow cytometry (see below , step 7). cDC1: Gr1 − CD11c + CD11b low/− XCR1 + ; cDC2: Gr1 − CD11c + CD11b + XCR1 − ; pDC: Gr1 − CD11c + CD11b − B220 + .

Article Snippet: CD135 (Flt3) PerCP-Cy5.5 (A2F10) , eBioscience , 46-1351-82.

Techniques: Flow Cytometry, Cell Culture

Reagents, enzymes, chemicals, and solutions <xref ref-type= a) " width="100%" height="100%">

Journal: European journal of immunology

Article Title: Guidelines for mouse and human DC generation

doi: 10.1002/eji.202249816

Figure Lengend Snippet: Reagents, enzymes, chemicals, and solutions a)

Article Snippet: CD135 (Flt3) PerCP-Cy5.5 (A2F10) , eBioscience , 46-1351-82.

Techniques: Modification, Saline, Recombinant

Proposed guidelines to ensure of the identity of the DC types generated in vitro, as compared to cells of the monocyte/macrophage lineages

Journal: European journal of immunology

Article Title: Guidelines for mouse and human DC generation

doi: 10.1002/eji.202249816

Figure Lengend Snippet: Proposed guidelines to ensure of the identity of the DC types generated in vitro, as compared to cells of the monocyte/macrophage lineages

Article Snippet: CD135 (Flt3) PerCP-Cy5.5 (A2F10) , eBioscience , 46-1351-82.

Techniques: Generated, In Vitro, Functional Assay, Expressing, Immunopeptidomics, Infection, Cell Stimulation