GRIN3A Antibody (C-term) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q8TCU5 |
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Clone Names | 91013076 |
Gene ID | 116443 |
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Other Names | Glutamate receptor ionotropic, NMDA 3A, GluN3A, N-methyl-D-aspartate receptor subtype 3A, NMDAR3A, NR3A, NMDAR-L, GRIN3A, KIAA1973 |
Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Name | GRIN3A |
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Synonyms | KIAA1973 |
Function | NMDA receptor subtype of glutamate-gated ion channels with reduced single-channel conductance, low calcium permeability and low voltage-dependent sensitivity to magnesium. Mediated by glycine. During the development of neural circuits, plays a role in the synaptic refinement period, restricting spine maturation and growth. By competing with GIT1 interaction with ARHGEF7/beta-PIX, may reduce GIT1/ARHGEF7-regulated local activation of RAC1, hence affecting signaling and limiting the maturation and growth of inactive synapses. May also play a role in PPP2CB-NMDAR mediated signaling mechanism. |
Cellular Location | Cell membrane {ECO:0000250|UniProtKB:Q9R1M7}; Multi-pass membrane protein. Postsynaptic cell membrane. Postsynaptic density. Note=Enriched in postsynaptic plasma membrane and postsynaptic densities. Requires the presence of GRIN1 to be targeted at the plasma membrane (By similarity). |
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Background
This gene encodes a subunit of the N-methyl-D-aspartate(NMDA) receptors, which belong to the superfamily ofglutamate-regulated ion channels, and function in physiological andpathological processes in the central nervous system. This subunitshows greater than 90% identity to the corresponding subunit inrat. Studies in the knockout mouse deficient in this subunitsuggest that this gene may be involved in the development ofsynaptic elements by modulating NMDA receptor activity. [providedby RefSeq].
References
Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010)Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :Ma, J.Z., et al. Hum. Genet. 127(5):503-512(2010)Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009)Liu, H.P., et al. Dement Geriatr Cogn Disord 28(6):521-527(2009)
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