
Thermo Fisher Scientific NMDAR2B Polyclonal Antibody
Rabbit 폴리클로날 항체로 NMDAR2B 단백질을 검출. Western blot, IHC, ICC/IF에 사용 가능. Mouse와 Rat에 반응하며, 학습 및 기억 관련 신경 연구에 적합. 고순도 친화성 크로마토그래피 정제, 냉동 보관 권장.
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:1,000 |
| Immunohistochemistry (IHC) | 1:500 |
| Immunocytochemistry (ICC/IF) | 1:400 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Synthetic peptide corresponding to the N-terminal region of the NR2B subunit of rat GRIN2B conjugated to KLH |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification | Affinity chromatography |
| Storage Buffer | 0.01M HEPES, pH 7.5, with 0.15M NaCl, 100µg/mL BSA, 50% glycerol |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| RRID | AB_10986289 |
Product Specific Information
This antibody is predicted to react with bovine, canine, chicken, human, mouse, and non-human primate based on 100% sequence homology.
Target Information
NMDAR2B is a member of the N-methyl-D-aspartate (NMDA) class of ionotropic glutamate receptors. NMDA receptors (NMDAR) are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie memory and learning processes.
NMDARs play a role in neuronal development and have been implicated in several central nervous system disorders such as Alzheimer’s disease, epilepsy, and ischemic neuronal cell death. Overexpression of the NR2B subunit is associated with enhanced learning and memory, whereas reduced NR2B expression is observed in aged or memory-impaired animals.
Phosphorylation at Tyr1472 on NR2B may increase NMDAR expression at the synapse, contributing to synaptic plasticity. NMDAR2B forms a heterotrimer composed of seven genetically encoded and differentially expressed subunits, including NR1, NR2, and NR3. Dysfunction of NMDAR2B is associated with epileptic encephalopathy and autosomal dominant mental retardation.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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