Revision 1

#38554Store at -20C

1 Kit

(6 x 20 microliters)

Cell Signaling Technology

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For Research Use Only. Not for Use in Diagnostic Procedures.
Product Includes Product # Quantity Mol. Wt Isotype/Source
Doublecortin (E6O6A) Rabbit mAb 91954 20 µl 45 kDa Rabbit IgG
NCAM1 (CD56) (E7X9M) XP® Rabbit mAb 99746 20 µl 120 to 220 kDa Rabbit IgG
NeuroD1 (D90G12) Rabbit mAb 7019 20 µl 49 kDa Rabbit IgG
β3-Tubulin (D71G9) XP® Rabbit mAb 5568 20 µl 55 kDa Rabbit IgG
TBR1 (D6C6X) Rabbit mAb 49661 20 µl 74 kDa Rabbit IgG
Stathmin (D1Y5A) Rabbit mAb 13655 20 µl 19 kDa Rabbit IgG
Anti-rabbit IgG, HRP-linked Antibody 7074 100 µl Goat 

Please visit cellsignal.com for individual component applications, species cross-reactivity, dilutions, protocols, and additional product information.

Description

The Immature Neuron Marker Antibody Sampler Kit provides an economical means for detecting immature neuron proteins by western blot. The kit includes enough antibodies to perform two western blot experiments with each primary antibody.

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

Background

The antibodies in this kit serve to characterize and identify immature neurons. During development, radial glia (RG) cells located in the ventricular zone (VZ) of the brain divide asymmetrically, each producing a neuronal and RG daughter cell. The daughter RG cell is also known as a neural progenitor cell (NPC) or an intermediate progenitor cell (IPC). Newly formed IPCs migrate to the subventricular zone (SVZ) where they divide symmetrically, each giving rise to two post-mitotic neurons that can then migrate to their final destination. In adulthood, NPCs reside within the subgranular zone (SGZ) of the dentate gyrus, and the adult SVZ, which surrounds the lateral ventricles of the cerebral cortex. NPCs within the SGZ and SVZ divide and give rise to immature neurons (1). The cytoskeleton of these cells plays an important role in generating neuronal processes. The cytoskeleton consists of three types of cytosolic fibers: actin microfilaments, intermediate filaments, and microtubules. β3-tubulin is one of six β-tubulin isoforms that make up the building blocks of microtubules (2). Stathmin is a tubulin binding protein that regulates microtubule dynamics in a phosphorylation dependent manner. Stathmin is heavily expressed during neuronal development, mediating differentiation and synaptic plasticity (3,4). Doublecortin is a microtubule-associated protein that facilitates neurite outgrowth and cell migration (5). The dual expression of doublecortin and NCAM (neural cell adhesion molecule, CD56), combined with the lack of expression of mature neuronal markers, is evidence of an immature neuronal phenotype (6). NCAM mediates neuronal attachment, neurite extension, and cell to cell interactions through homo and heterophilic interactions. Polysialic acid (PSA) post-translational modification of NCAM disrupts cell to cell adhesion, promoting axonal growth, cell migration, and synaptic plasticity during neurogenesis (7-9).

Transcription factors also play a key role in immature neuron growth and differentiation. NeuroD1 is a member of the basic helix-loop-helix (bHLH) family of transcription factors. These proteins function by forming heterodimers with E-proteins and binding to the canonical E-box sequence CANNTG (10,11). Neuronal activity results in CaMKII-mediated phosphorylation of NeuroD1 at Ser336, which is necessary for the formation and growth of dendrites (12,13). T-box, brain, 1 (TBR1) is a transcription factor important in vertebrate embryo development. As a member of the T-Box family of transcription factors, TBR1 is expressed in postmitotic glutamatergic projection neurons (14). During cortical neurogenesis, sequential expression of transcription factors Pax6, TBR2, and TBR1 regulates discrete steps in projection neuron differentiation (15).

  1. Martínez-Cerdeño, V. and Noctor, S.C. (2018) Front Neuroanat 12, 104.
  2. Jiang, Y.Q. and Oblinger, M.M. (1992) J Cell Sci 103 (Pt 3), 643-51.
  3. Chauvin, S. and Sobel, A. (2015) Prog Neurobiol 126, 1-18.
  4. Uchida, S. et al. (2014) Nat Commun 5, 4389.
  5. Reiner, O. et al. (2004) Cell Cycle 3, 747-51.
  6. Coviello, S. et al. (2022) Front Neuroanat 16, 851432.
  7. Seidenfaden, R. et al. (2003) Mol Cell Biol 23, 5908-18.
  8. Bonfanti, L. and Seki, T. (2021) Cells 10, 2542.
  9. Wędzony, K. et al. (2013) Pharmacol Rep 65, 1471-8.
  10. Schonhoff, S.E. et al. (2004) Endocrinology 145, 2639-44.
  11. Sharma, A. et al. (1999) Mol Cell Biol 19, 704-13.
  12. Chae, J.H. et al. (2004) Mol Cells 18, 271-88.
  13. Gaudillière, B. et al. (2004) Neuron 41, 229-41.
  14. Hevner, R.F. et al. (2001) Neuron 29, 353-66.
  15. Englund, C. et al. (2005) J Neurosci 25, 247-51.

Background References

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    Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
    XP is a registered trademark of Cell Signaling Technology, Inc.
    KARPAS cell line source: Dr. Abraham Karpas at the University of Cambridge.
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