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anti human straightfrom whole blood cd66b microbeads  (Miltenyi Biotec)


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    Miltenyi Biotec anti human straightfrom whole blood cd66b microbeads
    Anti Human Straightfrom Whole Blood Cd66b Microbeads, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cd66b+microbeads/StraightFrom+Whole+Blood+CD66b+MicroBeads%2C+human/pm41999502-33-5-11
    Average 94 stars, based on 17 article reviews
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    Purification:

    Article Title: Ferroptotic Neutrophils Induce Immunosuppression and Chemoresistance in Breast Cancer
    Article Snippet: 1 Ferroptotic Neutrophils Induce Immunosuppression and 1 Chemoresistance in Breast Cancer 2 Running Title: Ferroptotic neutrophils drive breast cancer chemoresistance 3 4 Wenfeng Zeng1, 2, #, Ruihua Zhang1, 2, #, Penghan Huang1, 2, #, Minxia Chen1, 2, Houying 5 Chen1, 2, Xin Zeng1, Jiang Liu1, 2, Jiahui Zhang1, 2, *, Di Huang1, 2, *, Liyan Lao1, 2, * 6 7 1Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene 8 Regulation, Medical Research Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen 9 University, Guangzhou 510120, China 10 2Breast Tumor Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, 11 Guangzhou 510120, China 12 13 # These authors contributed equally to the manuscript.. 14 15 *Corresponding authors: 16 Liyan Lao, 107 Yanjiang West Road, Guangzhou 510120, China; 86-20-87332022; 17 laoly3@mail.sysu.edu.cn 18 Di Huang, 107 Yanjiang West Road, Guangzhou 510120, China; 86-20-87332022; 19 huangd63@mail.sysu.edu.cn 20 Jiahui Zhang, 107 Yanjiang West Road, Guangzhou 510120, China; 86-20-87332022; 21 D ow nloaded from http://aacrjournals.org/cancerres/article-pdf/doi/10.1158/0008-5472.C AN -24-1941/3517591/can-24-1941.pdf by guest on 08 D ecem ber 2024 2 zhangjh28@mail2.sysu.edu.cn 22 23 Conflict of interest: The authors declare no competing interests.. 24 25 Significance 26 In chemoresistant breast cancer, IL-1+CXCL3+CD4+ T cells mediate neutrophil 27 ferroptosis that suppresses antitumor immunity, indicating that interfering with this 28 intercellular crosstalk could be an attractive strategy to reverse chemoresistance.

    Cytometry:

    Article Title: Ferroptotic Neutrophils Induce Immunosuppression and Chemoresistance in Breast Cancer
    Article Snippet: 1 Ferroptotic Neutrophils Induce Immunosuppression and 1 Chemoresistance in Breast Cancer 2 Running Title: Ferroptotic neutrophils drive breast cancer chemoresistance 3 4 Wenfeng Zeng1, 2, #, Ruihua Zhang1, 2, #, Penghan Huang1, 2, #, Minxia Chen1, 2, Houying 5 Chen1, 2, Xin Zeng1, Jiang Liu1, 2, Jiahui Zhang1, 2, *, Di Huang1, 2, *, Liyan Lao1, 2, * 6 7 1Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene 8 Regulation, Medical Research Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen 9 University, Guangzhou 510120, China 10 2Breast Tumor Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, 11 Guangzhou 510120, China 12 13 # These authors contributed equally to the manuscript.. 14 15 *Corresponding authors: 16 Liyan Lao, 107 Yanjiang West Road, Guangzhou 510120, China; 86-20-87332022; 17 laoly3@mail.sysu.edu.cn 18 Di Huang, 107 Yanjiang West Road, Guangzhou 510120, China; 86-20-87332022; 19 huangd63@mail.sysu.edu.cn 20 Jiahui Zhang, 107 Yanjiang West Road, Guangzhou 510120, China; 86-20-87332022; 21 D ow nloaded from http://aacrjournals.org/cancerres/article-pdf/doi/10.1158/0008-5472.C AN -24-1941/3517591/can-24-1941.pdf by guest on 08 D ecem ber 2024 2 zhangjh28@mail2.sysu.edu.cn 22 23 Conflict of interest: The authors declare no competing interests.. 24 25 Significance 26 In chemoresistant breast cancer, IL-1+CXCL3+CD4+ T cells mediate neutrophil 27 ferroptosis that suppresses antitumor immunity, indicating that interfering with this 28 intercellular crosstalk could be an attractive strategy to reverse chemoresistance.

    Isolation:

    Article Title: NK Cells and PMN-MDSCs in the Graft From G-CSF Mobilized Haploidentical Donors Display Distinct Gene Expression Profiles From Those of the Non-Mobilized Counterpart
    Article Snippet: .. NK cells and PMN-MDSCs were isolated from PBMCs of mobilized and non-mobilized donors using NK isolation kit and CD66b + microbeads (purity >98%, data not shown) following manufacturer’s instruction (Miltenyi Biotec, Bergisch Gladbach, Germany). .. Before starting any experiment, we determined the purity of isolated cells by flow cytometry using anti-CD3-APC, anti-CD19-ECD, and CD56-PC7 (Beckman Coulter, Brea, CA) for NK cells.

    Flow Cytometry:

    Article Title: Ferroptotic Neutrophils Induce Immunosuppression and Chemoresistance in Breast Cancer
    Article Snippet: Erythrocytes were removed from neutrophils with RBC lysis buffer (eBioscience, #00-4333-57). .. Peripheral neutrophils were purified with CD66b microbeads (Miltenyi Biotec, #130-104-913) and confirmed by flow cytometry. ..



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    Immunophenotypic analysis of peripheral blood neutrophil granulocytes from axiom mission 3 (Ax-3) crew (A) A schematic illustrating the time points of blood draw and layout of the 18 days long (18days) Ax-3 mission to International Space Station (ISS). Preflight blood samples were collected on one day before the launch (L-1d) and postflight blood samples were collected on one day after the return (R+1day). (B) Peripheral blood was subjected to density gradient centrifugation and normal-density neutrophils (NDN, >1.077 g/mL)) and low-density neutrophils (LDN, <1.077 g/mL) were isolated. This figure was created in BioRender (Esendagli, G. (2025) https://BioRender.com/a4m1kdr ). (C) Representative flow cytometry dot-plots of the <1.077 g/mL blood fraction are shown from an astronaut. Red population depicts the LDN cells determined after back gating the CD11b + HLA-DR - <t>CD66b</t> + cells found among the peripheral blood mononuclear cells (PBMC). (D) Percentage of LDN determined at preflight and postflight analyses. Each dot represents a member of the Ax-3 crew. (E) Granularity (SSC) and size (FSC) values of NDN and LDN were quantified by flow cytometry. (F) Flow cytometry offset histograms of neutrophil cell surface markers associated with cellular activation are demonstrated for a representative astronaut. Autofluorescence (AF) values were taken as technical control. (G) Percentage of NDN and LDN populations positive for CD11b, CD33, CD62L, CD80, CD86, and CD69 markers. (H) Expression levels of the neutrophil surface molecules was calculated by normalizing the median fluorescence intensity (MFI) to AF for each marker and a comparative heatmap was prepared (A.U., arbitrary units). Statistical analyses were performed with paired t test (∗ p ≤ 0.05, ∗∗ p ≤ 0.01, ∗∗∗ p ≤ 0.001). The p values calculated to be > 0.05 were not indicated. The data are presented as mean with standard error of mean (SEM).
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    Immunophenotypic analysis of peripheral blood neutrophil granulocytes from axiom mission 3 (Ax-3) crew (A) A schematic illustrating the time points of blood draw and layout of the 18 days long (18days) Ax-3 mission to International Space Station (ISS). Preflight blood samples were collected on one day before the launch (L-1d) and postflight blood samples were collected on one day after the return (R+1day). (B) Peripheral blood was subjected to density gradient centrifugation and normal-density neutrophils (NDN, >1.077 g/mL)) and low-density neutrophils (LDN, <1.077 g/mL) were isolated. This figure was created in BioRender (Esendagli, G. (2025) https://BioRender.com/a4m1kdr ). (C) Representative flow cytometry dot-plots of the <1.077 g/mL blood fraction are shown from an astronaut. Red population depicts the LDN cells determined after back gating the CD11b + HLA-DR - <t>CD66b</t> + cells found among the peripheral blood mononuclear cells (PBMC). (D) Percentage of LDN determined at preflight and postflight analyses. Each dot represents a member of the Ax-3 crew. (E) Granularity (SSC) and size (FSC) values of NDN and LDN were quantified by flow cytometry. (F) Flow cytometry offset histograms of neutrophil cell surface markers associated with cellular activation are demonstrated for a representative astronaut. Autofluorescence (AF) values were taken as technical control. (G) Percentage of NDN and LDN populations positive for CD11b, CD33, CD62L, CD80, CD86, and CD69 markers. (H) Expression levels of the neutrophil surface molecules was calculated by normalizing the median fluorescence intensity (MFI) to AF for each marker and a comparative heatmap was prepared (A.U., arbitrary units). Statistical analyses were performed with paired t test (∗ p ≤ 0.05, ∗∗ p ≤ 0.01, ∗∗∗ p ≤ 0.001). The p values calculated to be > 0.05 were not indicated. The data are presented as mean with standard error of mean (SEM).
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    Immunophenotypic analysis of peripheral blood neutrophil granulocytes from axiom mission 3 (Ax-3) crew (A) A schematic illustrating the time points of blood draw and layout of the 18 days long (18days) Ax-3 mission to International Space Station (ISS). Preflight blood samples were collected on one day before the launch (L-1d) and postflight blood samples were collected on one day after the return (R+1day). (B) Peripheral blood was subjected to density gradient centrifugation and normal-density neutrophils (NDN, >1.077 g/mL)) and low-density neutrophils (LDN, <1.077 g/mL) were isolated. This figure was created in BioRender (Esendagli, G. (2025) https://BioRender.com/a4m1kdr ). (C) Representative flow cytometry dot-plots of the <1.077 g/mL blood fraction are shown from an astronaut. Red population depicts the LDN cells determined after back gating the CD11b + HLA-DR - <t>CD66b</t> + cells found among the peripheral blood mononuclear cells (PBMC). (D) Percentage of LDN determined at preflight and postflight analyses. Each dot represents a member of the Ax-3 crew. (E) Granularity (SSC) and size (FSC) values of NDN and LDN were quantified by flow cytometry. (F) Flow cytometry offset histograms of neutrophil cell surface markers associated with cellular activation are demonstrated for a representative astronaut. Autofluorescence (AF) values were taken as technical control. (G) Percentage of NDN and LDN populations positive for CD11b, CD33, CD62L, CD80, CD86, and CD69 markers. (H) Expression levels of the neutrophil surface molecules was calculated by normalizing the median fluorescence intensity (MFI) to AF for each marker and a comparative heatmap was prepared (A.U., arbitrary units). Statistical analyses were performed with paired t test (∗ p ≤ 0.05, ∗∗ p ≤ 0.01, ∗∗∗ p ≤ 0.001). The p values calculated to be > 0.05 were not indicated. The data are presented as mean with standard error of mean (SEM).
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    Immunophenotypic analysis of peripheral blood neutrophil granulocytes from axiom mission 3 (Ax-3) crew (A) A schematic illustrating the time points of blood draw and layout of the 18 days long (18days) Ax-3 mission to International Space Station (ISS). Preflight blood samples were collected on one day before the launch (L-1d) and postflight blood samples were collected on one day after the return (R+1day). (B) Peripheral blood was subjected to density gradient centrifugation and normal-density neutrophils (NDN, >1.077 g/mL)) and low-density neutrophils (LDN, <1.077 g/mL) were isolated. This figure was created in BioRender (Esendagli, G. (2025) https://BioRender.com/a4m1kdr ). (C) Representative flow cytometry dot-plots of the <1.077 g/mL blood fraction are shown from an astronaut. Red population depicts the LDN cells determined after back gating the CD11b + HLA-DR - <t>CD66b</t> + cells found among the peripheral blood mononuclear cells (PBMC). (D) Percentage of LDN determined at preflight and postflight analyses. Each dot represents a member of the Ax-3 crew. (E) Granularity (SSC) and size (FSC) values of NDN and LDN were quantified by flow cytometry. (F) Flow cytometry offset histograms of neutrophil cell surface markers associated with cellular activation are demonstrated for a representative astronaut. Autofluorescence (AF) values were taken as technical control. (G) Percentage of NDN and LDN populations positive for CD11b, CD33, CD62L, CD80, CD86, and CD69 markers. (H) Expression levels of the neutrophil surface molecules was calculated by normalizing the median fluorescence intensity (MFI) to AF for each marker and a comparative heatmap was prepared (A.U., arbitrary units). Statistical analyses were performed with paired t test (∗ p ≤ 0.05, ∗∗ p ≤ 0.01, ∗∗∗ p ≤ 0.001). The p values calculated to be > 0.05 were not indicated. The data are presented as mean with standard error of mean (SEM).
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    Immunophenotypic analysis of peripheral blood neutrophil granulocytes from axiom mission 3 (Ax-3) crew (A) A schematic illustrating the time points of blood draw and layout of the 18 days long (18days) Ax-3 mission to International Space Station (ISS). Preflight blood samples were collected on one day before the launch (L-1d) and postflight blood samples were collected on one day after the return (R+1day). (B) Peripheral blood was subjected to density gradient centrifugation and normal-density neutrophils (NDN, >1.077 g/mL)) and low-density neutrophils (LDN, <1.077 g/mL) were isolated. This figure was created in BioRender (Esendagli, G. (2025) https://BioRender.com/a4m1kdr ). (C) Representative flow cytometry dot-plots of the <1.077 g/mL blood fraction are shown from an astronaut. Red population depicts the LDN cells determined after back gating the CD11b + HLA-DR - <t>CD66b</t> + cells found among the peripheral blood mononuclear cells (PBMC). (D) Percentage of LDN determined at preflight and postflight analyses. Each dot represents a member of the Ax-3 crew. (E) Granularity (SSC) and size (FSC) values of NDN and LDN were quantified by flow cytometry. (F) Flow cytometry offset histograms of neutrophil cell surface markers associated with cellular activation are demonstrated for a representative astronaut. Autofluorescence (AF) values were taken as technical control. (G) Percentage of NDN and LDN populations positive for CD11b, CD33, CD62L, CD80, CD86, and CD69 markers. (H) Expression levels of the neutrophil surface molecules was calculated by normalizing the median fluorescence intensity (MFI) to AF for each marker and a comparative heatmap was prepared (A.U., arbitrary units). Statistical analyses were performed with paired t test (∗ p ≤ 0.05, ∗∗ p ≤ 0.01, ∗∗∗ p ≤ 0.001). The p values calculated to be > 0.05 were not indicated. The data are presented as mean with standard error of mean (SEM).
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    Immunophenotypic analysis of peripheral blood neutrophil granulocytes from axiom mission 3 (Ax-3) crew (A) A schematic illustrating the time points of blood draw and layout of the 18 days long (18days) Ax-3 mission to International Space Station (ISS). Preflight blood samples were collected on one day before the launch (L-1d) and postflight blood samples were collected on one day after the return (R+1day). (B) Peripheral blood was subjected to density gradient centrifugation and normal-density neutrophils (NDN, >1.077 g/mL)) and low-density neutrophils (LDN, <1.077 g/mL) were isolated. This figure was created in BioRender (Esendagli, G. (2025) https://BioRender.com/a4m1kdr ). (C) Representative flow cytometry dot-plots of the <1.077 g/mL blood fraction are shown from an astronaut. Red population depicts the LDN cells determined after back gating the CD11b + HLA-DR - <t>CD66b</t> + cells found among the peripheral blood mononuclear cells (PBMC). (D) Percentage of LDN determined at preflight and postflight analyses. Each dot represents a member of the Ax-3 crew. (E) Granularity (SSC) and size (FSC) values of NDN and LDN were quantified by flow cytometry. (F) Flow cytometry offset histograms of neutrophil cell surface markers associated with cellular activation are demonstrated for a representative astronaut. Autofluorescence (AF) values were taken as technical control. (G) Percentage of NDN and LDN populations positive for CD11b, CD33, CD62L, CD80, CD86, and CD69 markers. (H) Expression levels of the neutrophil surface molecules was calculated by normalizing the median fluorescence intensity (MFI) to AF for each marker and a comparative heatmap was prepared (A.U., arbitrary units). Statistical analyses were performed with paired t test (∗ p ≤ 0.05, ∗∗ p ≤ 0.01, ∗∗∗ p ≤ 0.001). The p values calculated to be > 0.05 were not indicated. The data are presented as mean with standard error of mean (SEM).
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    Immunophenotypic analysis of peripheral blood neutrophil granulocytes from axiom mission 3 (Ax-3) crew (A) A schematic illustrating the time points of blood draw and layout of the 18 days long (18days) Ax-3 mission to International Space Station (ISS). Preflight blood samples were collected on one day before the launch (L-1d) and postflight blood samples were collected on one day after the return (R+1day). (B) Peripheral blood was subjected to density gradient centrifugation and normal-density neutrophils (NDN, >1.077 g/mL)) and low-density neutrophils (LDN, <1.077 g/mL) were isolated. This figure was created in BioRender (Esendagli, G. (2025) https://BioRender.com/a4m1kdr ). (C) Representative flow cytometry dot-plots of the <1.077 g/mL blood fraction are shown from an astronaut. Red population depicts the LDN cells determined after back gating the CD11b + HLA-DR - <t>CD66b</t> + cells found among the peripheral blood mononuclear cells (PBMC). (D) Percentage of LDN determined at preflight and postflight analyses. Each dot represents a member of the Ax-3 crew. (E) Granularity (SSC) and size (FSC) values of NDN and LDN were quantified by flow cytometry. (F) Flow cytometry offset histograms of neutrophil cell surface markers associated with cellular activation are demonstrated for a representative astronaut. Autofluorescence (AF) values were taken as technical control. (G) Percentage of NDN and LDN populations positive for CD11b, CD33, CD62L, CD80, CD86, and CD69 markers. (H) Expression levels of the neutrophil surface molecules was calculated by normalizing the median fluorescence intensity (MFI) to AF for each marker and a comparative heatmap was prepared (A.U., arbitrary units). Statistical analyses were performed with paired t test (∗ p ≤ 0.05, ∗∗ p ≤ 0.01, ∗∗∗ p ≤ 0.001). The p values calculated to be > 0.05 were not indicated. The data are presented as mean with standard error of mean (SEM).
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    Immunophenotypic analysis of peripheral blood neutrophil granulocytes from axiom mission 3 (Ax-3) crew (A) A schematic illustrating the time points of blood draw and layout of the 18 days long (18days) Ax-3 mission to International Space Station (ISS). Preflight blood samples were collected on one day before the launch (L-1d) and postflight blood samples were collected on one day after the return (R+1day). (B) Peripheral blood was subjected to density gradient centrifugation and normal-density neutrophils (NDN, >1.077 g/mL)) and low-density neutrophils (LDN, <1.077 g/mL) were isolated. This figure was created in BioRender (Esendagli, G. (2025) https://BioRender.com/a4m1kdr ). (C) Representative flow cytometry dot-plots of the <1.077 g/mL blood fraction are shown from an astronaut. Red population depicts the LDN cells determined after back gating the CD11b + HLA-DR - CD66b + cells found among the peripheral blood mononuclear cells (PBMC). (D) Percentage of LDN determined at preflight and postflight analyses. Each dot represents a member of the Ax-3 crew. (E) Granularity (SSC) and size (FSC) values of NDN and LDN were quantified by flow cytometry. (F) Flow cytometry offset histograms of neutrophil cell surface markers associated with cellular activation are demonstrated for a representative astronaut. Autofluorescence (AF) values were taken as technical control. (G) Percentage of NDN and LDN populations positive for CD11b, CD33, CD62L, CD80, CD86, and CD69 markers. (H) Expression levels of the neutrophil surface molecules was calculated by normalizing the median fluorescence intensity (MFI) to AF for each marker and a comparative heatmap was prepared (A.U., arbitrary units). Statistical analyses were performed with paired t test (∗ p ≤ 0.05, ∗∗ p ≤ 0.01, ∗∗∗ p ≤ 0.001). The p values calculated to be > 0.05 were not indicated. The data are presented as mean with standard error of mean (SEM).

    Journal: iScience

    Article Title: Spaceflight alters the immune regulatory functions of neutrophil granulocytes on T lymphocytes

    doi: 10.1016/j.isci.2025.114380

    Figure Lengend Snippet: Immunophenotypic analysis of peripheral blood neutrophil granulocytes from axiom mission 3 (Ax-3) crew (A) A schematic illustrating the time points of blood draw and layout of the 18 days long (18days) Ax-3 mission to International Space Station (ISS). Preflight blood samples were collected on one day before the launch (L-1d) and postflight blood samples were collected on one day after the return (R+1day). (B) Peripheral blood was subjected to density gradient centrifugation and normal-density neutrophils (NDN, >1.077 g/mL)) and low-density neutrophils (LDN, <1.077 g/mL) were isolated. This figure was created in BioRender (Esendagli, G. (2025) https://BioRender.com/a4m1kdr ). (C) Representative flow cytometry dot-plots of the <1.077 g/mL blood fraction are shown from an astronaut. Red population depicts the LDN cells determined after back gating the CD11b + HLA-DR - CD66b + cells found among the peripheral blood mononuclear cells (PBMC). (D) Percentage of LDN determined at preflight and postflight analyses. Each dot represents a member of the Ax-3 crew. (E) Granularity (SSC) and size (FSC) values of NDN and LDN were quantified by flow cytometry. (F) Flow cytometry offset histograms of neutrophil cell surface markers associated with cellular activation are demonstrated for a representative astronaut. Autofluorescence (AF) values were taken as technical control. (G) Percentage of NDN and LDN populations positive for CD11b, CD33, CD62L, CD80, CD86, and CD69 markers. (H) Expression levels of the neutrophil surface molecules was calculated by normalizing the median fluorescence intensity (MFI) to AF for each marker and a comparative heatmap was prepared (A.U., arbitrary units). Statistical analyses were performed with paired t test (∗ p ≤ 0.05, ∗∗ p ≤ 0.01, ∗∗∗ p ≤ 0.001). The p values calculated to be > 0.05 were not indicated. The data are presented as mean with standard error of mean (SEM).

    Article Snippet: StraightFrom® Whole Blood CD66b MicroBeads, human , Miltenyi , Cat # 130-104-913.

    Techniques: Gradient Centrifugation, Isolation, Flow Cytometry, Activation Assay, Control, Expressing, Fluorescence, Marker