CD11b (Microglia) MicroBeads, human and mouse

Name: CD11b (Microglia) MicroBeads, human and mouse
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CD11b (Microglia) MicroBeads, human and mouse

Product overview

CD11b (Microglia) MicroBeads have been developed for the positive isolation of primary mouse and human CD11b

⁺

microglia. The purification protocol takes approx. one hour.

Product data and images for CD11b (Microglia) MicroBeads, human and mouse

Figures

Figure 1

Whole-brain tissue from P1 mice was first dissociated to single cells using the Neural Tissue Dissociation Kit (T) and then microglia were isolated using CD11b (Microglia) MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells are fluorescently stained with CD11b-APC and CD45-FITC.

Before separation	Microglia CD11b ⁺ fraction
View details Figure 1 Whole-brain tissue from P1 mice was first dissociated to single cells using the Neural Tissue Dissociation Kit (T) and then microglia were isolated using CD11b (Microglia) MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells are fluorescently stained with CD11b-APC and CD45-FITC.	View details Figure 1 Whole-brain tissue from P1 mice was first dissociated to single cells using the Neural Tissue Dissociation Kit (T) and then microglia were isolated using CD11b (Microglia) MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells are fluorescently stained with CD11b-APC and CD45-FITC.

Specifications for CD11b (Microglia) MicroBeads, human and mouse

Overview

CD11b (Microglia) MicroBeads have been developed for the positive isolation of primary mouse and human CD11b

⁺

microglia. The purification protocol takes approx. one hour.

Detailed product information

Background information

Microglia, often called brain macrophages, are the resident immune effector cells in the central nervous system (CNS). In addition, activated microglia serve as the major antigen-presenting cells in the CNS. They are morphologically, immunophenotypically, and functionally related to cells of the monocyte/macrophage lineage.

This detailed protocol using CD11b (Microglia) MicroBeads allows the fast isolation of primary microglia within 1 hour. The use of the MACS Neural Tissue Dissociation Kit (P) prior to the purification leads to highest yield and viability.

For the isolation of microglia from myelin-containing tissue samples (human tissue or adult mouse or rat), the use of Myelin Removal Beads II is highly recommended.

Downstream applications

CD11b (Microglia) MicroBeads have been used to isolate CD11b

⁺

cells from single-cell suspensions of brain tissue

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Columns

MS, LS, XS, or autoMACS

^®

Columns.

Resources for CD11b (Microglia) MicroBeads, human and mouse

Documents and Protocols

Brochures/posters

Neuroscience - Inspiring technologies for creative scientists

Scientific posters

Efficient isolation of viable primary neural cells from adult murine brain tissue based on a novel automated tissue dissociation protocol. Zhang, H. et al. SfN (2016)

Scientific posters

Semi-automated tissue dissociation and preserved epitope integrity optimize immunomagnetic sorting of neural cells

Protocols

Isolation of microglia from adult mouse or rat brain

Reviews for CD11b (Microglia) MicroBeads, human and mouse

Easy to Use Microglia Purification

CD11b (Microglia) MicroBeads, human and mouse, small size (130-093-636)

This kit provides clear instructions and good yield (~90%) of microglia purification with CD11b+ selection.

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References for CD11b (Microglia) MicroBeads, human and mouse

Publications

Justin, A. et al. (2012) The Ifng gene is essential for Vdr gene expression and vitamin D3-mediated reduction of the pathogenic T cell burden in the central nervous system in experimental autoimmune encephalomyelitis, a multiple sclerosis model. J. Immunol. 189: 3188-3197
Lauren, L. et al. (2011) Microglia and memory: modulation by early-life infection. J. Neurosci. 31: 15511-15521
Kremer, M. et al. (2010) Reduced immunoproteasome formation and accumulation of immunoproteasomal precursors in the brains of lymphocytic choriomeningitis virus-Infected mice. J. Immunol. 185: 5549-5560
Lee, J. K. et al. (2008) Regulator of G-protein signaling 10 promotes dopaminergic neuron survival via regulation of the microglial inflammatory response. J. Neurosci. 28: 8517-8528
Su, W. et al. (2014) The p53 transcription factor modulates microglia behavior through microRNA-dependent regulation of c-maf. J. Immunol. 192: 358-366
Zhang, X. et al. (2014) Peripheral role of cathepsin S in Tʜ1 cell-dependent transition of nerve injury-induced acute pain to a chronic pain state. J. Neurosci. 34: 3013-3022
Woodling, N. S. et al. (2014) Suppression of alzheimer-associated inflammation by microglial prostaglandin-E2 EP4 receptor signaling. J. Neurosci. 34: 5882-5894
Kleinberger, G. et al. (2014) TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis. Sci Transl Med 6: 243ra86
Cho, S.-H. et al. (2015) SIRT1 deficiency in microglia contributes to cognitive decline in aging and neurodegeneration via epigenetic regulation of IL-1β. J. Neurosci. 35: 807-818
Zeiner, P. S. et al. (2014) MIF receptor CD74 is restricted to microglia/macrophages, associated with a M1-polarized immune milieu and prolonged patient survival in gliomas. Brain Pathol. 25: 491-504
Kiris, E. et al. (2015) Dysregulation of glutamine transporter SNAT1 in rett syndrome microglia: a mechanism for mitochondrial dysfunction and neurotoxicity. J. Neurosci. 35: 2516-2529

Data and images