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anti mouse cd103 pe  (Elabscience Biotechnology)


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    Elabscience Biotechnology anti mouse cd103 pe
    Anti Mouse Cd103 Pe, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+mouse+cd103+pe/PE+Anti-Mouse+CD103+Antibody/pm41286853-95-18-21
    Average 93 stars, based on 5 article reviews
    anti mouse cd103 pe - by Bioz Stars, 2026-10
    93/100 stars

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    other:

    Article Title: Butyrate ameliorates ulcerative colitis through targeting STING-dependent ER stress signaling and limiting CD4 + TRM T cells accumulation
    Article Snippet: The following antibodies were used: (1) anti-Mouse CD4-PerCP-Cy5.5 (E-AB-F1353J, Elabscience, China), (2) anti-Mouse CD69-APC (E-AB-F1187E, Elabscience, China), (3) anti-Mouse CD103-PE (E-AB-F1090D, Elabscience, China).

    Article Title: Butyrate ameliorates ulcerative colitis through targeting STING-dependent ER stress signaling and limiting CD4 + TRM T cells accumulation.
    Article Snippet: The following antibodies were used: (1) anti-Mouse CD4-PerCP-Cy5.5 (E-AB-F1353J, Elabscience, China), (2) anti-Mouse CD69-APC (E-AB-F1187E, Elabscience, China), (3) anti-Mouse CD103-PE (E-AB-F1090D, Elabscience, China).



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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