Recombinant Mouse Netrin-G2a Fc Chimera Protein, CF Summary
Product Specifications
Mouse Netrin-G2a (Asp18 - Arg504) Accession # NP_598007 |
IEGRMDP | Mouse IgG2A (Glu98 - Lys330) |
N-terminus | C-terminus | |
Analysis
Product Datasheets
Carrier Free
CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.
In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.
2744-NG
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
Reconstitution | Reconstitute at 400 μg/mL in PBS. |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Reconstitution Calculator
Background: Netrin-G2a
Netrin-G2a (netr: Sanskrit for "one who guides") is a 60 ‑ 75 kDa glycoprotein member of the netrin‑G/laminet subfamily, UNC-6/netrin family of axon guidance molecules (1, 2, 3). The two members of the netrin‑G subfamily (G1 and G2) are GPI‑linked and found only in vertebrates. They do not bind to either DCC or UNC5, but regulate synaptic interactions by binding to NGL-1 and NGL-2. Mouse Netrin-G2a (also called laminet-2 and NTNG2) is the shortest of three netrin‑G2 gene products (2). It is synthesized as a 530 amino acid (aa) preprocursor that contains a 17 aa signal sequence, a 490 aa mature region, and a 23 aa C‑terminal prosegment that is cleaved to give rise to a GPI‑linkage site (Gly507). The mature molecule contains one N‑terminal laminin type VI domain (aa 60 ‑ 285), plus three consecutive laminin EGF‑like regions (aa 287 ‑ 453). There are at least two splice variants, each of which show insertions after Gly352. The first (netrin‑G2b) shows a 60 aa substitution for Asn353, while the second (netrin‑G2c) shows a 35 aa substitution for Asn353. Mature mouse Netrin‑G2a shares 99% and 96% aa identity with rat and human Netrin‑G2a, respectively. Netrin‑G2a is principally expressed in neurons, including granule cells of the dentate gyrus, pyramidal cells of the hippocampus (CA1, CA3, CA4) and cells of the cerebral cortex (4, 5, 6). It appears to be a presynaptic molecule that is associated with excitatory intracortical tracts (6 ‑ 9). The ligand for Netrin‑G2a is NGL‑2/netrin‑G ligand #2, a postsynaptic 100 kDa member of the NGL family of synaptic cell adhesion molecules (8, 10). Netrin‑G2a:NGL‑2 binding is of high affinity (KD = 2.5 nM), and appears to influence the stability of NMDA‑type glutamatergic receptors on postsynaptic membranes (4, 11). Although the exact mechanism is unclear, Netrin‑G2a ligation of NGL‑2 promotes NGL-2 interaction with PSD95 and NR1 and NR2B in the postsynaptic membrane. This leads to an association of both neuroligin‑1/2 and NMDA subunits, and the formation of functional, fixed glutamatergic receptors (5, 6, 8).
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Yin, Y. et al. (2002) Mol. Cell. Neurosci. 19:344.
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Nakashiba, T. et al. (2002) Mech. Dev. 111:47.
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Meerabux, J. et al. (2005) Genomics 86:112.
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Eastwood, S.L. & P.J. Harrison (2008) Neuropsychpharmacology 33:933.
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Pan, Y. et al. (2010) Exp. Neurol. Apr. 9 [Epub ahead of print].
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Nishimura-Akiyoshi, S. et al. (2007) Proc. Natl. Acad. Sci. USA 104:14801.
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Miyashita, T. et al. (2005) Neuroscience 136:487.
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Kim, S. et al. (2006) Nat. Neurosci. 9:1294.
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Niimi, K. et al. (2007) J. Neuroimmunol. 192:99.
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Woo, J. et al. (2009) Mol. Cell. Neurosci. 42:1.
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Zhang, W. et al. (2008) Genes Brain Behav. 7:385.
Citation for Recombinant Mouse Netrin-G2a Fc Chimera Protein, CF
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
1 Citation: Showing 1 - 1
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The Spinal Transcriptome after Cortical Stroke: In Search of Molecular Factors Regulating Spontaneous Recovery in the Spinal Cord
Authors: J Kaiser, M Maibach, I Salpeter, N Hagenbuch, VBC de Souza, MD Robinson, ME Schwab
J. Neurosci., 2019-04-08;39(24):4714-4726.
Species: Rat
Sample Types: Whole Cells
Applications: Bioassay
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