Phospho-GluR1 (S845) Antibody Summary
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of Phospho-GluR1 (S845) by Western Blot. Western blot of rat hippocampal lysate showing specific immunolabeling of the ~100 kDa GluR1 protein phosphorylated at S845 (Control). The phosphospecificity of this labeling is demonstrated by treatment with 1200 U of lambda Phosphatase ( lambda -PPase) for 30 minutes before being exposed to the Anti-Phospho-GluR1 (S845). The immunolabeling is completely eliminated by treatment with lambda -PPase.
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Preparation and Storage
Background: GluR1
Rat GluR1 is a 907 amino acid, 4-transmembrane protein that belongs to the glutamate-gated ion channel family. It is one of four AMPA receptor subunits that form a functional heterotetrameric glutamate receptor. GluR1 only interacts with GluR2. GluR1 has two key serine residues in the C-terminal extracellular region. Serine 831 is constitutively unphosphorylated. Upon exposure to a neurotransmitter, it is phosphorylated by CaMKII leading to a potentiation of glutamate-mediated current. Serine 845 is constitutively phosphorylated by Protein Kinase A (PKA). The presence of the phosphate insures membrane localization of the subunit. Following NMDA receptor activation, S845 is dephosphorylated with subsequent subunit internalization.
Product Datasheets
Citations for Phospho-GluR1 (S845) Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Dopamine dependent effects on basal and glutamate stimulated network dynamics in cultured hippocampal neurons
Authors: Yan Li
J. Neurochem, 2017-01-12;0(0):.
Species: Mouse
Sample Types: Cell Lysates
Applications: Western Blot -
Soluble ICAM-5, a Product of Activity Dependent Proteolysis, Increases mEPSC Frequency and Dendritic Expression of GluA1
Authors: Irina Lonskaya, John Partridge, Rupa R. Lalchandani, Andrew Chung, Taehee Lee, Stefano Vicini et al.
PLoS ONE
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