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| Overview |
| The Anti-PSA-NCAM antibodies can be used for the identification and enumeration of human, mouse, and rat PSA-NCAM+ cells by flow cytometry, fluorescence microscopy, or immunohistochemistry. |
| Details |
Background information
Anti-PSA-NCAM MicroBeads recognize polysialic acid (PSA), which is linked to the extracellular domain of the neural cell adhesion molecule (NCAM, CD56).1 PSA-NCAM, the highly polysialated form of NCAM, is predominantly expressed in embryonic and neonatal neural tissue.2 In adult mammalian brain PSA-NCAM expression is restricted mainly to areas that retain neurogenic potential, such as the subventricular zone (SVZ)3 and the dentate gyrus of the hippocampus.4 PSA-NCAM is a marker for immature neuronal-committed progenitors that are permanently generated in the SVZ and migrate along a well-defined pathway, the rostral migratory stream, into the olfactory bulb where they differentiate into GABAergic and dopaminergic interneurons.3,5 PSA-NCAM positive neuronal precursors have been isolated from rat forebrain and from mouse SVZ tissue in conjunction with prior depletion of A2B5+ glial progenitor cells.6-10 |
| Clone | Isotype |
| 2-2B | Mouse IgM |
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| Figure 1 |
| Mouse brain tissue postnatal day 1 was dissociated using the Neural Tissue Dissociation Kit (T). Brain cells were stained with Anti-PSA-NCAM-PE (A) or Anti-PSA-NCAM-APC (B). Cells were analyzed by flow cytometry. |
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| B |
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| Favorites / Prices |
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| Details |
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| Products |
| Anti-PSA-NCAM-PE, human, mouse, rat |
- for 100 tests (1)
Download datasheet
130-093-274
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| Anti-PSA-NCAM-APC, human, mouse, rat |
- for 100 tests (1)
Download datasheet
130-093-273
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| (1) One test corresponds to fluorescent labeling of up to 106 cells in a total volume of 100 µL. |
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| References |
| 1. Rougon, G. and Marshak, D.R. (1986) J. Biol. Chem. 261: 3396–3401. |
| 2. Kiss, J.Z. and Muller, D. (2001) Rev. Neurosci. 12: 297–310. |
| 3. Doetsch et al. (1997) J. Neurosci. 17: 5046–5061. |
| 4. Seki (2002) J. Neurosci. Res. 70: 327–334. |
| 5. Pennartz et al. (2004) Mol. Cell. Neurosci. 25: 692–706. |
| 6. Seidenfaden et al. (2006) Mol. Cell. Neurosci. 32: 187–98. |
| 7. Seidenfaden et al. (2006) MACS&more 10(1): 4–6. |
| 8. Marmur et al. (1998) J. Neurosci. 18: 9800–9811. |
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