Grin2b Antibody

Code CSB-PA191146
Size US$297
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  • Western blot analysis of extract from T98G cells using NMDANR2B Subunit Antibody
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Product Details

Full Product Name
Rabbit anti-Rattus norvegicus (Rat) Grin2b Polyclonal antibody
Uniprot No.
Target Names
Grin2b
Alternative Names
Grin2bGlutamate receptor ionotropic antibody; NMDA 2B antibody; GluN2B antibody; Glutamate [NMDA] receptor subunit epsilon-2 antibody; N-methyl D-aspartate receptor subtype 2B antibody; NMDAR2B antibody; NR2B antibody
Raised in
Rabbit
Species Reactivity
Human,Mouse,Rat
Immunogen
Peptide sequence around aa.1250-1254(N-L-Y-D-I) derived from Human NMDANR2B Subunit.
Immunogen Species
Rattus norvegicus (Rat)
Clonality
Polyclonal
Purification Method
Antibodies were produced by immunizing rabbits with synthetic peptide and KLH conjugates. Antibodies were purified by affinity-chromatography using epitope-specific peptide.
Concentration
It differs from different batches. Please contact us to confirm it.
Form
Supplied at 1.0mg/mL in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Tested Applications
ELISA,WB
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:1000
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Component of NMDA receptor complexes that function as heterotetrameric, ligand-gated ion channels with high calcium permeability and voltage-dependent sensitivity to magnesium. Channel activation requires binding of the neurotransmitter glutamate to the epsilon subunit, glycine binding to the zeta subunit, plus membrane depolarization to eliminate channel inhibition by Mg(2+). Sensitivity to glutamate and channel kinetics depend on the subunit composition (Probable). In concert with DAPK1 at extrasynaptic sites, acts as a central mediator for stroke damage. Its phosphorylation at Ser-1303 by DAPK1 enhances synaptic NMDA receptor channel activity inducing injurious Ca2+ influx through them, resulting in an irreversible neuronal death. Contributes to neural pattern formation in the developing brain. Plays a role in long-term depression (LTD) of hippocampus membrane currents and in synaptic plasticity.
Gene References into Functions
  1. CaMKIIa-GluN2B interaction had an important role in the development of L-dopa-induced dyskinesia. PMID: 30142538
  2. Peptides specifically disrupting the interaction between GluN2B and AP-2 complex not only blocked endocytosis of GluN2B induced by NMDA treatment but also abolished NMDA-induced excitotoxicity PMID: 28326942
  3. the BDNF-Fyn-GluN2B signaling cascade in the spinal dorsal horn may constitute a key mechanism underlying central sensitization and neuropathic pain development after peripheral nerve injury PMID: 28497343
  4. Pharmacological inactivation and antagonism study suggests that oflactory span capacity in rats depends on GluN2B-containing NMDA receptor-dependent interactions between the medial prefrontal cortex and dorsomedial striatum. PMID: 28916627
  5. APP intracellular domain increase in mature neurons, as reported in Alzheimer's disease, alters synaptic NMDAR composition to an immature-like GluN2B-rich profile. This disrupts synaptic signal integration, via over-activation of SK channels, and synapse plasticity. PMID: 28682239
  6. Findings provide a new insight for the role of GluN2B in memory storage in adult hippocampus. The unique mechanism, by which GluN2B is training-strength-dependently involved in memory formation, suggests that GluN2B can flexibly participate in memory formation through a rapid change in its membrane expression following individual experience. PMID: 27487820
  7. An appetitive experience after fear memory destabilization attenuates fear retention. Blocking GluN2B-NMDA receptors in basolateral amygdala, prevented the fear reduction caused by the appetitive experience. Results suggest that the expression of a fear memory can be dampened by an unrelated appetitive experience, as long as memory destabilization is achieved during reactivation. PMID: 27531837
  8. This study demonstrated that high anxiety restraint rats had decreased GR/GluN2B density in cortical areas and basolateral amygdala. PMID: 27865917
  9. Transgenic rats with over-expressed GluN2B-subunits in the forebrain exhibited a relatively higher susceptibility to morphine-induced conditioned place preference (CPP) and naloxone-induced place aversion than their wild-type littermates did, while they retained the similar sensitivity as wild-type rats to CPP induced by natural reinforcers (food and sucrose). PMID: 27217103
  10. Overexpression of EphB2 also rescued the ADDLs-induced depletion of the expression of EphB2 and GluN2B-containing NMDA receptors trafficking in cultured hippocampal neurons. PMID: 28358367
  11. Results are consistent with a role of GluN2B diheretomers in long-term depression, a role of both GluN2B- and GluN2D- containing NMDARs in short-term potentiation and a role of GluN2A/B triheteromers in long-term potentiation. PMID: 27523302
  12. single nucleotide polymorphism (SNP) sites in the rat GRIN2B promoter region were screened. PMID: 25917873
  13. While low-frequency stimulation -depotentiation clearly required N-Methyl-D-aspartate (NMDA) receptor activation, GluN2B-containing NMDA receptors were not involved in this form of depotentiation. PMID: 26881126
  14. Data show that 17beta estradiol recruits a causal role for GluN2B-containing NMDARs and ERK signaling in the induction of long-term potentiation PMID: 26190171
  15. activity-dependent regulation of STEP61 and its substrates GluN2B and GluA2 may contribute to homeostatic stabilization of excitatory synapses. PMID: 26391783
  16. Results show that monomeric Abeta1-42 application induces an increase of the Ca2+-response and of the membrane expression of the extrasynaptic subunit of the NMDA receptor GluN2B in PC12 cells, while the opposite effects were observed in cultured neurons PMID: 26401567
  17. The NR2B-CREB-CRTC1 signaling pathway may play a crucial role in circadian rhythm of pain PMID: 26440419
  18. The pronociception induced by systemic cholecystokinin, which is vagal afferent-dependent, requires activation of central amygdala NR2B-containing N-methyl-d-aspartate receptors. PMID: 26197883
  19. The adaptive changes in AMPAR and NMDAR subunit mRNA might dictate the regenerative fate of FMNs in response to the peripheral axotomy and thereby play a unique role in the pathogenesis of facial nerve injury and regeneration. PMID: 26343542
  20. Study reported that in the developing rat cortex, migration of presumptive layer II/III neurons to their deserved destination was regulated by NMDA receptors with GluN2B subunit PMID: 25838242
  21. Auditory cortex NR2B mRNA and protein were upregulated in salicylate-treated rats. expression returning to normal levels 14 days after cessation of treatment or after GM1 administration. PMID: 26554229
  22. results revealed that the phosphorylation change of GluN2B at Tyr-1070 accompanied the Tyr-1472 phosphorylation and Fyn associated with GluN2B in synaptic plasticity induced by both chemical and contextual fear learning. PMID: 26229100
  23. Results suggest that the pre-synaptic facilitator NR2B subunit may contribute to epileptogenesis by triggering hyper-excitability and, in general, NMDARs containing NR2B may modulate an ERK 1/2-mediated NR2A over-expression PMID: 22824136
  24. Lovastatin downregulates excessive NR2B expression accompanied by increased expression of ERK signaling cascade. The effect of NR2B in upregulating pERK1/2 maybe due, at least in part, to inactivation of CaMKII/SAP102/SynGAP signaling cascade. PMID: 24718106
  25. increased after stress, and decreased in the CLF. NMDAR2B were increased in the hippocampus of CLF and CHF. In the amygdala, there was a decrease in the NMDAR2B for stress in the CLF and CHF. PMID: 25772108
  26. Here we have used single molecule fluorescence resonance energy transfer (smFRET) to investigate the cleft closure conformational states that the glycine-binding domain of the NMDA receptors PMID: 25404733
  27. Study demonstrates that hippocampal NR2B receptors play an important role in the enhanced LTP and visceral hypersensitivity in irritable bowel syndrome-like rats and that activities of NR2B-NMDARs are mainly regulated by tyrosine kinase PMID: 24824341
  28. the late adolescent acquisition of GluN2B function provides a mechanism for dopamine D1-mediated regulation of PFC responses in an input-specific manner. PMID: 24041503
  29. GluN2B subunits are moderately expressed at primary afferent synapses on lamina I NK1R+ neurons, but play more important roles for polysynaptic NMDA EPSCs driven by primary afferents following disinhibition PMID: 25122884
  30. In addition, PNS significantly increased the levels of GSK-3alpha, beta and NR2B, but reduced hippocampal cell proliferation during fear extinction. PMID: 24631206
  31. The specific temporospatial distribution pattern of CaMKII with NR2B might be related to the different physiological functions during postnatal development PMID: 22906554
  32. the developmental increase in synaptic expression of PSD95 obstructs the synaptic clustering of NR2B-NMDARs, and thereby restricts reactivation of dendritic branching. PMID: 24705401
  33. GluN2B receptor subtype decreases in the perirhinal cortex of methamphetamine induced-memory deficit animals. PMID: 24120858
  34. gp120 injures neurons via an increase of NR2B and a decrease of PSD-95 expressions PMID: 24491052
  35. Authors uncover a non-canonical mechanism by which GluN2B-NMDAR surface dynamics plays a critical role in the plasticity of maturing synapses through a direct interplay with CaMKII. PMID: 24591565
  36. Released Ca(2+) dissociates preformed CaMKIIalpha from mGluR5 and meanwhile promotes active CaMKIIalpha to bind to the adjacent NMDAR GluN2B subunit, which enables CaMKIIalpha to phosphorylate GluN2B at a CaMKIIalpha-sensitive site. PMID: 24032403
  37. Disrupting NR2B-Cdk5 interaction via a small interfering peptide (siP) increases NR2B surface levels, facilitates synaptic transmission, and improves memory formation in vivo. PMID: 24607229
  38. Data indicate that Wnt-5a signaling is related to nitric oxide (NO) production, which in turn increases the the GluN2B subunit of the NMDA receptor (NMDAR) trafficking to the cell surface. PMID: 24440698
  39. we used immunoblotting to investigate the role of an NMDAR subpopulation on the phosphorylation level of the GluN2B subunit at the Y1336 and Y1472 sites in rat brain slices after NMDA treatment. PMID: 23585298
  40. Prenatal activation of maternal TLR3 receptors by viral-mimetic poly(I:C) modifies GluN2B expression in embryos and sonic hedgehog in offspring in the absence of kynurenine pathway activation. PMID: 23981041
  41. Activation of NR2B receptors increases excitatory postsynaptic potentials in glycoprotein (gp)120-treated macrophages. PMID: 23660833
  42. increased expression as a key mechanisms for long-term synaptic plasticity in visceral pain hypersensitivity rats PMID: 24487031
  43. Increased expression of NR2B in the hippocampus is associated with amelioration of impaired fear extinction in stressed rats. PMID: 23584669
  44. Serine residue (Ser1166) in the carboxy-terminal tail Of GluN2B is a functional target of protein kinase A phosphorylation. PMID: 24431445
  45. Artificial food colors and additives led to an increase in NR2B and nAChR beta2 receptor subunits in male rats and led to decrease in NR2B subunits in female rats. PMID: 23429044
  46. NR2B-specific small interfering (si)RNA was neuroprotective against an animal model of Parkinson's disease. PMID: 22377595
  47. We find that synaptic N-methyl-D-aspartate receptor stimulation in neurons leads to activation of PP1 through a mechanism involving inhibitory phosphorylation at Thr320 by Cdk5. PMID: 24189275
  48. results implied that NR2B-, not NR2A-, containing NMDARs showed pathological high expression in AD-like rat hippocampus PMID: 22359056
  49. In the dyskinetic striatum, striatal GluN2B subunits tonically inhibit striato-nigral projections. PMID: 23611155
  50. synapses in chronically epileptic tissue can undergo an long-term potentiation enhancement due to an NR2B up-regulation in CA1 pyramidal neurons PMID: 23313317

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Subcellular Location
Cell membrane; Multi-pass membrane protein. Cell junction, synapse, postsynaptic cell membrane; Multi-pass membrane protein. Late endosome. Lysosome. Cytoplasm, cytoskeleton.
Protein Families
Glutamate-gated ion channel (TC 1.A.10.1) family, NR2B/GRIN2B subfamily
Tissue Specificity
Expressed in the hippocampus including the dentate gyrus (at protein level). Detected in adult olfactory bulb, brain cortex, hippocampus, striatum, thalamus, superior colliculus, with much lower levels in inferior colliculus, midbrain and cerebellum.
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