NMDA Receptor 1 (NMDAR1) (pTyr1336), (NR2B Subunit) antibody

Details for Product No. ABIN361484
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Antigen
Synonyms CG2902, DMNMDAR1, DNMDAR-I, DNmdar, DmelNmdar1, Dmel\\CG2902, DrNR1, NMDA, NMDA R1, NMDAR1, NMdar1, NR1, NRI, Nmdar, dNR1, dnmdar-I, nmr
Epitope
pTyr1336, NR2B Subunit
(6), (4), (4), (3), (3), (2), (2), (2), (1), (1), (1), (1), (1), (1)
Reactivity
Rat (Rattus)
(17), (2)
Host
Rabbit
(17)
Clonality
Polyclonal
Application
Western Blotting (WB), Immunohistochemistry (IHC)
(17), (5), (3), (2)
Pubmed 1 reference available
Quantity 100 μL
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Catalog No. ABIN361484
379.50 $
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Specificity Specific for ~180k NMDAR NR2B subunit protein phosphorylated at Tyr1336. Immunolabeling of the NMDAR NR2B subunit band is blocked by (-phosphatase treatment.
Purification Affinity-purified
Alternative Name NMDA Receptor
Background The NMDAR plays an essential role in memory, neuronal development and it has also been implicated in several disorders of the central nervous system including Alzheimer?s, epilepsy and ischemic neuronal cell death (Grosshans et al., 2002, Wenthold et al., 2003, Carroll and Zukin, 2002). The rat NMDAR1 (NR1) was the first subunit of the NMDAR to be cloned. The NR1 protein can form NMDA activated channels when expressed in Xenopus oocytes but the currents in such channels are much smaller than those seen in situ. Channels with more physiological characteristics are produced when the NR1 subunit is combined with one or more of the NMDAR2 (NR2 A-D) subunits (Ishii et al., 1993). Phosphorylation of Tyr1336 is thought to potentiate NMDA receptor-dependent influx of calcium (Takasu et al., 2002) and ischemia may also increase the phosphorylation of this site (Takagi et al., 2003). Anti-Phospho-Tyr1336 NMDA Receptor NR2B Subunit Western blot of rat hippocampal lysate showing specific immunolabeling of the ~180k NR2B subunit of the NMDAR phosphorylated at Tyr1336 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: (-Ptase). The blot is identical to the control except that it was incubated in (-Ptase (1200 units for 30 min) before being exposed to the phospho-Tyr1336 NMDA NR2B antibody. The immunolabeling is completely eliminated by treatment with (-Ptase.
Application Notes Recommended Dilution: WB: 1:1000 IHC: 1:400 Quality Control: Western blots performed on each lot.
Restrictions For Research Use only
Format Liquid
Storage -20 °C
Supplier Images
anti-NMDA Receptor 1 (NMDAR1) (pTyr1336), (NR2B Subunit) antibody Western blots of rat hippocampal lysate showing specific immunolabeling of the ~180k NR2B subunit of the NMDAR phosphorylated at Tyr1336 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: (-Ptase). The blot is identical to the control except that it was incubated in (-Ptase (1200 units for 30 min) before being exposed to the phospho-Tyr1336 NMDA NR2B antibody. The immunolabeling is completely eliminated by treatment with (-Ptase.
Product cited in: Jiang, Knox, Pathipati et al.: "Developmental localization of NMDA receptors, Src and MAP kinases in mouse brain." in: Neuroscience letters, Vol. 503, Issue 3, pp. 215-9, 2011 (PubMed).

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