<0.10 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Bioactivity
Theoretical MW
138 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
130-150 kDa, reducing conditions
Publications
Read Publication using 8207-CR in the following applications:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>90%, by SDS-PAGE with silver staining.
Reconstitution Instructions
Reconstitute at 250 μg/mL in PBS.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Caspr2 Protein, CF
AUTS15
Caspr2
CASPR2DKFZp781D1846
CDFE
Cell recognition molecule Caspr2
CNTNAP2
contactin associated protein-like 2
contactin-associated protein 2
contactin-associated protein-like 2
homolog of Drosophila neurexin IV
KIAA0868
NRXN4
NRXN4Caspr2
PTHSL1
Background
Contact-associated Protein-like 2 (Caspr2) is a type I transmembrane member of the neurexin family of adhesion molecules (1). Human Caspr2 is the vertebrate homolog to Drosophila Neurexin IV, and the human and mouse Caspr2 orthologs share 94% amino acid sequence identity. Human Caspr2 contains two EGF-like domains, one F5/8 type C domain, one fibrinogen C-terminal domain, and four laminin G-like domains. It is highly expressed in neuronal tissue where it is primarily localized to the juxtaparanodal region of the axonal membrane (1, 2). Caspr2 acts in conjunction with 4.1B and Tag-1 as a scaffold that clusters Kv1 potassium channels at the juxtaparanodal region and is critical for axo-glial contacts (1-6). Caspr2 interacts with carboxypeptidase E in Golgi bodies during intracellular trafficking to the cell membrane (7). Caspr2 is also required for dendrite arborization and the normal development of neural networks (8). Mutations in Caspr2 are associated with predisposition to autism spectrum disorders, epilepsy, attention-deficit hyperactive disorder, and schizophrenia (8-11). The presence of autoantibodies against Caspr2 is associated with encephalitis, epilepsy, dysarthria, and paroxysmal kinesigenic dystonia (12-14). R&D Systems in-house testing indicates that Caspr2 can enhance bovine corneal endothelial cell adhesion.
Poliak, S. et al. (1999) Neuron 24:1037.
Poliak, S. et al. (2001) J. Neurosci. 21:7568.
Horresh, I. et al. (2010) J. Neurosci. 30:2480.
Traka, M. et al. (2003) J. Cell Biol. 162:1161.
Denisenko-Nehrbass, N. et al. (2003) Eur. J. Neurosci. 17:411.
Poliak, S. et al. (2003) J. Cell Biol. 162:1149.
Oiso, S. et al. (2009) J. Neurochem. 109:158.
Anderson, G.R. et al. (2012) Proc. Natl. Acad. Sci. USA 109:18120.
Penagarikano, O. and D.H. Geschwind (2012) Trends Mol. Med. 18:156.
Friedman, J.I. et al. (2008) Mol. Psychiatry 13:261.
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