Recombinant Human DSCAM Protein, CF Summary
Details of Functionality |
Measured by its ability to bind biotinylated rhDSCAM in a functional ELISA with an apparent KD <10 nM. |
Source |
Mouse myeloma cell line, NS0-derived human DSCAM protein Glu18-Met1595 |
Accession # |
|
N-terminal Sequence |
Glu18 |
Protein/Peptide Type |
Recombinant Proteins |
Gene |
DSCAM |
Purity |
>90%, by SDS-PAGE under reducing conditions and visualized by silver stain |
Endotoxin Note |
<1.0 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
175 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 |
180-195 kDa, reducing conditions |
Packaging, Storage & Formulations
Storage |
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 under reducing conditions and visualized by silver stain |
Reconstitution Instructions |
Reconstitute at 400 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 DSCAM Protein, CF
Background
Down syndrome cell adhesion molecule (DSCAM) is a 220 kDa type I transmembrane glycoprotein and member of the immunoglobulin superfamily (1). Human DSCAM, which maps to a Down syndrome region of chromosome 21q22.2-22.3, is synthesized as a 2012 amino acid (aa) precursor that contains a 17 aa signal sequence, a 1578 aa extracellular domain (ECD), a 21 aa transmembrane segment, and a 396 aa cytoplasmic tail (SwissProt #: O60469). The ECD contains ten Ig-like C2-type domains, six fibronectin type-III domains, and 16 potential sites for N-linked glycosylation. Splicing variants lead to a second, shorter isoform, which has a ten aa substitution for aa 1562 - 1571 in the longer isoform, and a deletion of residues corresponding to aa 1572 - 2012 in the longer isoform. Human mature DSCAM is 98% aa identical to mature mouse and rat DSCAM. Studies on mice have shown that DSCAM is expressed widely in the developing nervous system (1 - 2). More recent studies indicate that DSCAM plays an important role in neurite arborization, cell body spacing, and lamina-specific synaptic targeting in vertebrate retina (2 - 4). DSCAM signaling in vertebrates is not well understood, but it has been shown that DSCAM directly binds to Pak1 and stimulates Pak1 phosphorylation and activity (5). In addition, DSCAM activates both JNK and p38 MAP kinases, and expression of the cytoplasmic domain of DSCAM induces a morphological change in cultured cells that is JNK-dependent (5). Thus, it appears that DSCAM signals through Pak1 and functions in axon guidance. Furthermore, DSCAM, in collaboration with DCC, interacts with netrin-1, and is a receptor required for netrin-dependent commissural axon outgrowth and pathfinding (2, 6).
- Yamakawa, K. et al. (1998) Hum. Mol. Genet. 7:227.
- Liu, G. et al. (2009) Proc. Natl. Acad. Sci. U.S.A. 106:2951.
- Fuerst, P.G. et al. (2008) Nature 451:470.
- Yamagata, M. and J.R. Sanes, 2008, Nature 451:465.
- Li, W. and K.-L. Guan (2004) J. Biol. Chem. 279:32824.
- Ly, A. et al. (2008) Cell 133:11241.
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