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  • 产品名称：anti-GluN2B(AA42-60)antibody

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  • 产品厂商：SYSY
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简单介绍：
anti-GluN2B(AA42-60)antibody
详情介绍：
Immunogen Synthetic peptide (aa 42-60 of rat GluN 2B) coupled to key-hole limpet hemocyanin via an added N-terminal cysteine residue.
Specificity Specific for GluN 2B
Cross-Reactivity (Details) no cross-reactivity to GluN 2A.
Purification Affinity purified with the immunogen. Rabbit serum albumin was added for stabilization.
Background Synonyms: NMDA-receptor 2B
Application Notes WB: 1 : 1000 (AP staining)
ICC: not tested yet
IHC: not tested yet
Comment

IP: For most effective IP use the solubilization protocol described in the ELISA protocol. Consider that protein-protein interaction may be affected.
Restrictions For Research Use only
Format Lyophilized
Reconstitution For reconstitution add 50 μL H2O to get a 1mg/ml solution of antibody in PBS. Then aliquot and store at -20 °C until use.
Buffer PBS
Handling Advice Affinity purified antibodies are less robust than antisera, since protease inhibitors are also removed during purification. Hence, storage at 4?°C for prolonged periods (i.e. several weeks), is not recommended.
Storage -20 °C
Storage Comment Unlabeled lyophilized antibodies are stable in this form without loss of quality at ambient temperatures for several weeks or even months. They can be stored at 4°C for several years. Lyophilized antibodies must not be stored in the freezer, they may be destroyed!
Supplier Images
Western Blotting (WB) image for anti-GluN 2B (AA 42-60) antibody (ABIN1742497) anti-GluN 2B (AA 42-60) antibody
Product cited in: Szutorisz, DiNieri, Sweet, Egervari, Michaelides, Carter, Ren, Miller, Blitzer, Hurd: "Parental THC exposure leads to compulsive heroin-seeking and altered striatal synaptic plasticity in the subsequent generation." in: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, Vol. 39, Issue 6, pp. 1315-23, 2014 (PubMed).

Gut, Beske, Hubbard, Lyman, Hamilton, McNutt: "Novel application of stem cell-derived neurons to evaluate the time- and dose-dependent progression of excitotoxic injury." in: PLoS ONE, Vol. 8, Issue 5, pp. e64423, 2013 (PubMed).