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pe anti cd103 rea789  (Miltenyi Biotec)


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    Miltenyi Biotec pe anti cd103 rea789
    Pe Anti Cd103 Rea789, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pe+anti+mouse+cd103/CD103+Antibody%2C+anti-mouse%2C+REAfinity/pmc12461889-28-0-5
    Average 93 stars, based on 15 article reviews
    pe anti cd103 rea789 - by Bioz Stars, 2026-09
    93/100 stars

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    Immunopeptidomics:

    Article Title: NR4A3 deficiency ameliorates contact hypersensitivity and exacerbates psoriasis by regulating gene expression in dendritic cells
    Article Snippet: DMSO (07-4860-5, Sigma Aldrich), LPS (L3024, Wako), and R848 (AG-CR1-3582-M005, AdipoGen) were purchased from the indicated sources. .. The following antibodies were used in flowcytometry, which were obtained from indicated sources: APC anti-mouse I-A/I-E (MHC II) (clone M5/114.15.2, BioLegend, 1:500), FITC anti-mouse I-A/I-E (MHC II) (clone M5/114.15.2, BioLegend, 1:500), PerCP anti-mouse I-A/I-E (MHC II) (clone M5/114.15.2, BioLegend, 1:250), PerCP anti-mouse CD3ε (clone 145-2C11, BioLegend, 1:100), FITC anti-mouse CD4 (clone GK1.5, BioLegend, 1:400), PECy7 anti-mouse CD4 (clone GK1.5, Tonbo Biosciences, 1:1000), VioGreen anti-mouse CD8a (clone 53-6-7, Myltenyi Biotec, 1:20), APCCy7 anti-human/mouse CD11b (clone M1/70, Tonbo Biosciences, 1:2000), PECy7 anti-mouse CD11c (clone N418, Tonbo Biosciences, 1:1000), PerPC/Cy5.5 anti-mouse CD24 (clone M1/69, BioLegend, 1:500), FITC anti-human/mouse CD44 (clone IM7, BioLegend, 1:100), FITC anti-mouse/human CD45R/B220 (clone RA3-6B2, BioLegend, 1:100), PE anti-mouse CD62L (clone MEL-14, Tonbo Biosciences, 1:100), FITC anti-mouse CD86 (clone GL-1, BioLegend, 1:100), PE anti-mouse CD103 (clone 2E7, Myltenyi Biotec, 1:20), APC anti-mouse CD172a/SIRPα (clone P84, BioLegend, 1:100), PE anti-mouse CD197/CCR7 (clone 4B12, BioLegend, 1:100), FITC anti-mouse CD207/Langerin (clone caa8-28H10, Myltenyi Biotec, 1:20), PE anti-mouse CD287/TLR7 (clone A94B10, BioLegend, 1:100), APC anti-mouse CD326/EpCAM (clone caa7-9G8, Myltenyi Biotec, 1:100), FITC anti-mouse TCRγδ (clone UC7-1305, BioLegend, 1:1000), PE/Cyanine7 anti-mouse IFN-γ (clone XMG1.2, BioLegend, 1:1000), PE anti-mouse IL-4 (clone 11B11, BioLegend, 1:100), PE anti-mouse IL-17A (TC11-18H10.1, BioLegend, 1:1000). ..



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    Fig. 3 The expression of CD31 and α-SMA in clinical samples and the anti-angiogenic therapy promotes infiltration of <t>CD103+CD8+</t> TRMs in tumor. A The expression of CD31 and α-SMA in CRC and CRC liver metastasis tissue. B The infiltra- tion level of CD103+CD8+ TRMs in the α-SMA high and low groups. C Comparison of median number and interquar- tile range of CD103+CD8+ TRMs. D The relationship of CD103+CD8+ TRMs and α-SMA+ vessel. E–F The infil- tration level of CD103+CD8+ TRMs in CRC patients who responded and non-respond to bevacizumab treatment. G Average tumor growth curves showing tumor volume in mice treated with either control or the Bevacizumab (n = 5 mice per group). H–K Representative flow cytometry plots (H) and the percentage of CD103+CD8+ TRMs (I) and representative flow cytometry plots (J) and the percentage of IFN-γ+ CD103+CD8+ TRMs (K) isolated from mice on day 21 (n = 5 mice per group). (Immunofluorescent staining, × 400, The white triangle in the tissue is CD103+CD8+ TRMs). CRC, colorectal cancer; TRM, tissue-resident memory T cell. α-SMA, alpha-smooth muscle actin. *p < 0.05; **p < 0.01; ***p < 0.001
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    Fig. 3 The expression of CD31 and α-SMA in clinical samples and the anti-angiogenic therapy promotes infiltration of <t>CD103+CD8+</t> TRMs in tumor. A The expression of CD31 and α-SMA in CRC and CRC liver metastasis tissue. B The infiltra- tion level of CD103+CD8+ TRMs in the α-SMA high and low groups. C Comparison of median number and interquar- tile range of CD103+CD8+ TRMs. D The relationship of CD103+CD8+ TRMs and α-SMA+ vessel. E–F The infil- tration level of CD103+CD8+ TRMs in CRC patients who responded and non-respond to bevacizumab treatment. G Average tumor growth curves showing tumor volume in mice treated with either control or the Bevacizumab (n = 5 mice per group). H–K Representative flow cytometry plots (H) and the percentage of CD103+CD8+ TRMs (I) and representative flow cytometry plots (J) and the percentage of IFN-γ+ CD103+CD8+ TRMs (K) isolated from mice on day 21 (n = 5 mice per group). (Immunofluorescent staining, × 400, The white triangle in the tissue is CD103+CD8+ TRMs). CRC, colorectal cancer; TRM, tissue-resident memory T cell. α-SMA, alpha-smooth muscle actin. *p < 0.05; **p < 0.01; ***p < 0.001
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    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: Inhibition of HCK in myeloid cells restricts pancreatic tumor growth and metastasis

    doi: 10.1016/j.celrep.2022.111479

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: PE hamster anti-mouse CD103 (Clone 2E7) , eBioscience , Cat#12–1031-82.

    Techniques: Blocking Assay, Avidin-Biotin Assay, Plasmid Preparation, RNA Sequencing, Software

    Fig. 3 The expression of CD31 and α-SMA in clinical samples and the anti-angiogenic therapy promotes infiltration of CD103+CD8+ TRMs in tumor. A The expression of CD31 and α-SMA in CRC and CRC liver metastasis tissue. B The infiltra- tion level of CD103+CD8+ TRMs in the α-SMA high and low groups. C Comparison of median number and interquar- tile range of CD103+CD8+ TRMs. D The relationship of CD103+CD8+ TRMs and α-SMA+ vessel. E–F The infil- tration level of CD103+CD8+ TRMs in CRC patients who responded and non-respond to bevacizumab treatment. G Average tumor growth curves showing tumor volume in mice treated with either control or the Bevacizumab (n = 5 mice per group). H–K Representative flow cytometry plots (H) and the percentage of CD103+CD8+ TRMs (I) and representative flow cytometry plots (J) and the percentage of IFN-γ+ CD103+CD8+ TRMs (K) isolated from mice on day 21 (n = 5 mice per group). (Immunofluorescent staining, × 400, The white triangle in the tissue is CD103+CD8+ TRMs). CRC, colorectal cancer; TRM, tissue-resident memory T cell. α-SMA, alpha-smooth muscle actin. *p < 0.05; **p < 0.01; ***p < 0.001

    Journal: Cancer immunology, immunotherapy : CII

    Article Title: Tissue-resident memory CD103+CD8+ T cells in colorectal cancer: its implication as a prognostic and predictive liver metastasis biomarker.

    doi: 10.1007/s00262-024-03709-2

    Figure Lengend Snippet: Fig. 3 The expression of CD31 and α-SMA in clinical samples and the anti-angiogenic therapy promotes infiltration of CD103+CD8+ TRMs in tumor. A The expression of CD31 and α-SMA in CRC and CRC liver metastasis tissue. B The infiltra- tion level of CD103+CD8+ TRMs in the α-SMA high and low groups. C Comparison of median number and interquar- tile range of CD103+CD8+ TRMs. D The relationship of CD103+CD8+ TRMs and α-SMA+ vessel. E–F The infil- tration level of CD103+CD8+ TRMs in CRC patients who responded and non-respond to bevacizumab treatment. G Average tumor growth curves showing tumor volume in mice treated with either control or the Bevacizumab (n = 5 mice per group). H–K Representative flow cytometry plots (H) and the percentage of CD103+CD8+ TRMs (I) and representative flow cytometry plots (J) and the percentage of IFN-γ+ CD103+CD8+ TRMs (K) isolated from mice on day 21 (n = 5 mice per group). (Immunofluorescent staining, × 400, The white triangle in the tissue is CD103+CD8+ TRMs). CRC, colorectal cancer; TRM, tissue-resident memory T cell. α-SMA, alpha-smooth muscle actin. *p < 0.05; **p < 0.01; ***p < 0.001

    Article Snippet: And 1 μl of fluorescein isothiocyanate (FITC) anti-mouse CD8 (cat. 11-0081-81, eBioScience), phycoerythrin (PE) anti-mouse CD103 (cat. E-AB-F1090D, Elabscience), and APC anti-mouse IFN-γ (cat. E-AB-F1101UE, Elabscience) were added to the tube, respectively.

    Techniques: Expressing, Comparison, Control, Flow Cytometry, Isolation, Staining