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CD271 (LNGFR) MicroBead Kit
Description
The CD271 (LNGFR) MicroBead Kit is an indirect labeling system for the immunomagnetic isolation of CD271 (LNGFR)+ cells. The kit includes all necessary reagents for fluorescent labeling (CD271 (LNGFR)-PE or -APC) and indirect magnetic labeling (Anti-PE or -APC MicroBeads) of CD271 (LNGFR)+ cells, as well as FcR Blocking Reagent for the prevention of unspecific labeling via Fc receptors.
CD271, also known as LNGFR (low-affinity nerve growth factor
receptor), NGFR (nerve growth factor receptor), or p75NTR
(neurotrophin receptor), belongs to the tumor necrosis factor
receptor superfamily. CD271 (LNGFR) was initially described to be
expressed on cells of the nervous system and was suggested to be
involved in the development, survival and differentiation of neural
cells.¹ CD271 (LNGFR) can be found in the central and peripheral
nervous system on autonomic and sensory neurons² as well as
on glial cells, including oligodendrocytes³, astrocytes⁓, Schwann
cells5,6, and neural crest precursors7.
Applications
  • Positive selection or depletion of cells expressing human CD271 (LNGFR).
    Positive selection of neural cells, including neural crest cells, motor neurons, and Schwann cells.
  • Columns
    MS, LS, XS, or autoMACSā„¢ Columns.
    Further information
    CD271_poster
    [PDF; 235,9 KB]
    Schwann cell isolation
    [PDF; 185 KB]
     
    Figure
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    Products
    CD271 MicroBead Kit (APC), human
    for 1Ɨ109 total cells
    Download data sheet
    130-092-283
    Qty:
     

    CD271 MicroBead Kit (PE), human
    for 1Ɨ109 total cells
    Download data sheet
    130-092-819
    Qty:
     

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    MACS References
    1. Thomson, T. M. et al. (1988) Exp. Cell Res. 174 (2): 533–539.
    2. Kashiba, H. et al. (1995) Brain Res. Mol. Brain
    Res. 30 (1): 158–164.
    3. Casaccia-Bonnefil, P. et al. (1996) Nature 383 (6602): 716–
    719.
    4. Rudge, J. S. et al. (1994) Eur J. Neurosci. 6 (5): 693–705.
    5. DiStefano, P. S. and Johnson, E. M. Jr. (1988) Proc. Natl. Acad. Sci. USA 85 (1): 270–274.
    6. Vroemen, M. and Weidner, N. (2003) J. Neuroscience Methods 124 (2): 135–143.
    7. Chalazonitis, A. et al. (1998) Dev Biol. 204 (2): 385–406.
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