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anti cd11b microbeads  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec anti cd11b microbeads
    Anti Cd11b Microbeads, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 85 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cd11b+microbeads/CD11b+MicroBeads+UltraPure%2C+mouse/pm42884680-126-38-41
    Average 95 stars, based on 85 article reviews
    anti cd11b microbeads - by Bioz Stars, 2026-11
    95/100 stars

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    Related Articles

    Isolation:

    Article Title: Temporary deterioration of health and behavior during pexidartinib-mediated microglia depletion and repopulation in progranulin-deficient mice
    Article Snippet: .. Primary microglia were isolated using the Miltenyi Adult Brain Dissociation Kit in combination with CD11b MicroBeads according to the manufacturer’s protocol. ..

    Single Cell:

    Article Title: Microglial SIRT6 confers protection against neuroinflammation-associated depression through NRF2-HO1 signaling
    Article Snippet: Tissue was enzymatically dissociated using the Neural Tissue Dissociation Kit (P) (130-092-628, Miltenyi Biotec) according to the manufacturer's protocol. .. Single-cell suspensions were incubated with CD11b MicroBeads (130-049-601, Miltenyi Biotec) for 15 min at 4 °C, followed by magnetic separation using MACS columns (130-042-401, Miltenyi Biotec). ..

    Incubation:

    Article Title: Microglial SIRT6 confers protection against neuroinflammation-associated depression through NRF2-HO1 signaling
    Article Snippet: Tissue was enzymatically dissociated using the Neural Tissue Dissociation Kit (P) (130-092-628, Miltenyi Biotec) according to the manufacturer's protocol. .. Single-cell suspensions were incubated with CD11b MicroBeads (130-049-601, Miltenyi Biotec) for 15 min at 4 °C, followed by magnetic separation using MACS columns (130-042-401, Miltenyi Biotec). ..

    Magnetic Cell Separation:

    Article Title: Microglial SIRT6 confers protection against neuroinflammation-associated depression through NRF2-HO1 signaling
    Article Snippet: Tissue was enzymatically dissociated using the Neural Tissue Dissociation Kit (P) (130-092-628, Miltenyi Biotec) according to the manufacturer's protocol. .. Single-cell suspensions were incubated with CD11b MicroBeads (130-049-601, Miltenyi Biotec) for 15 min at 4 °C, followed by magnetic separation using MACS columns (130-042-401, Miltenyi Biotec). ..

    other:

    Article Title: Epigenetic control of microglial mitochondrial immunity by KAT7 drives Alzheimer's disease pathogenesis.
    Article Snippet: The annealed crRNA and tracrRNA (IDT) were diluted in microinjection buffer (0.25 mM EDTA and 10 mM Tris-HCl, pH 7.4) and mixed with Cas9 protein (30 ng/μl; IDT) to obtain ctRNP complexes.

    Purification:

    Article Title: HIV transgenic mouse monocytes display increased in vivo migration across the blood-brain barrier associated with increased expression of genes associated with mononuclear leukocyte movement.
    Article Snippet: .. After highly purified monocytes (~98% CD11b+) from JRCCC mouse bone marrow leukocytes (BML) were obtained by immuno magnetic sorting using CD11b MicroBeads (Miltenyi Biotec), they were intravenously injected (20 × 106 cells/mouse) into B6 mice 4 h post-LPS or PBS treatment. ..

    Injection:

    Article Title: HIV transgenic mouse monocytes display increased in vivo migration across the blood-brain barrier associated with increased expression of genes associated with mononuclear leukocyte movement.
    Article Snippet: .. After highly purified monocytes (~98% CD11b+) from JRCCC mouse bone marrow leukocytes (BML) were obtained by immuno magnetic sorting using CD11b MicroBeads (Miltenyi Biotec), they were intravenously injected (20 × 106 cells/mouse) into B6 mice 4 h post-LPS or PBS treatment. ..



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    ( A ) Experimental timeline. ( B ) Representative confocal images at D4, D10, D30, and D45 showing that GFP is not co-labeled with TUJ1 or MAP2 in the brain. ( C ) Quantification of TUJ1 + GFP + double-positive cells among TUJ1 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( D ) Quantification of MAP2 + GFP + double-positive cells among MAP2 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( E ) Relative gene expression level at D18. N = 4 mice for each group. Data are presented as mean ± SD. Each data point represents one mouse.
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    ( A ) Experimental timeline. ( B ) Representative confocal images at D4, D10, D30, and D45 showing that GFP is not co-labeled with TUJ1 or MAP2 in the brain. ( C ) Quantification of TUJ1 + GFP + double-positive cells among TUJ1 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( D ) Quantification of MAP2 + GFP + double-positive cells among MAP2 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( E ) Relative gene expression level at D18. N = 4 mice for each group. Data are presented as mean ± SD. Each data point represents one mouse.
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    ( A ) Experimental timeline. ( B ) Representative confocal images at D4, D10, D30, and D45 showing that GFP is not co-labeled with TUJ1 or MAP2 in the brain. ( C ) Quantification of TUJ1 + GFP + double-positive cells among TUJ1 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( D ) Quantification of MAP2 + GFP + double-positive cells among MAP2 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( E ) Relative gene expression level at D18. N = 4 mice for each group. Data are presented as mean ± SD. Each data point represents one mouse.
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    ( A ) Experimental timeline. ( B ) Representative confocal images at D4, D10, D30, and D45 showing that GFP is not co-labeled with TUJ1 or MAP2 in the brain. ( C ) Quantification of TUJ1 + GFP + double-positive cells among TUJ1 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( D ) Quantification of MAP2 + GFP + double-positive cells among MAP2 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( E ) Relative gene expression level at D18. N = 4 mice for each group. Data are presented as mean ± SD. Each data point represents one mouse.
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    ( A ) Experimental timeline. ( B ) Representative confocal images at D4, D10, D30, and D45 showing that GFP is not co-labeled with TUJ1 or MAP2 in the brain. ( C ) Quantification of TUJ1 + GFP + double-positive cells among TUJ1 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( D ) Quantification of MAP2 + GFP + double-positive cells among MAP2 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( E ) Relative gene expression level at D18. N = 4 mice for each group. Data are presented as mean ± SD. Each data point represents one mouse.
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    ( A ) Experimental timeline. ( B ) Representative confocal images at D4, D10, D30, and D45 showing that GFP is not co-labeled with TUJ1 or MAP2 in the brain. ( C ) Quantification of TUJ1 + GFP + double-positive cells among TUJ1 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( D ) Quantification of MAP2 + GFP + double-positive cells among MAP2 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( E ) Relative gene expression level at D18. N = 4 mice for each group. Data are presented as mean ± SD. Each data point represents one mouse.
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    Image Search Results


    ( A ) Experimental timeline. ( B ) Representative confocal images at D4, D10, D30, and D45 showing that GFP is not co-labeled with TUJ1 or MAP2 in the brain. ( C ) Quantification of TUJ1 + GFP + double-positive cells among TUJ1 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( D ) Quantification of MAP2 + GFP + double-positive cells among MAP2 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( E ) Relative gene expression level at D18. N = 4 mice for each group. Data are presented as mean ± SD. Each data point represents one mouse.

    Journal: eLife

    Article Title: In vivo virus-free lineage tracing and live imaging reveal that NeuroD1 does not reprogram microglia into neurons

    doi: 10.7554/eLife.112083

    Figure Lengend Snippet: ( A ) Experimental timeline. ( B ) Representative confocal images at D4, D10, D30, and D45 showing that GFP is not co-labeled with TUJ1 or MAP2 in the brain. ( C ) Quantification of TUJ1 + GFP + double-positive cells among TUJ1 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( D ) Quantification of MAP2 + GFP + double-positive cells among MAP2 + cells at D4, D10, D30, and D45. N = 4 or 5 mice for each group. ( E ) Relative gene expression level at D18. N = 4 mice for each group. Data are presented as mean ± SD. Each data point represents one mouse.

    Article Snippet: The cell pellet was then resuspended in 90 μl of 0.5% BSA in DPBS and incubated with 10 μl of anti-CD11b magnetic beads (Miltenyi, Cat#: 130-097-142) for 30 min at 4°C.

    Techniques: Confocal, Labeling, Gene Expression, Magnetic Cell Separation, Real-time Polymerase Chain Reaction

    Using qPCR verify the relative expression of Neurod1 .

    Journal: eLife

    Article Title: In vivo virus-free lineage tracing and live imaging reveal that NeuroD1 does not reprogram microglia into neurons

    doi: 10.7554/eLife.112083

    Figure Lengend Snippet: Using qPCR verify the relative expression of Neurod1 .

    Article Snippet: The cell pellet was then resuspended in 90 μl of 0.5% BSA in DPBS and incubated with 10 μl of anti-CD11b magnetic beads (Miltenyi, Cat#: 130-097-142) for 30 min at 4°C.

    Techniques: Expressing, Gene Expression