R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
GluD1/GRID1 (E4Y3N) Rabbit mAb #71855
Filter:
- WB
Supporting Data
REACTIVITY | H M R |
SENSITIVITY | Endogenous |
MW (kDa) | 112 |
Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
Species Cross-Reactivity Key:
- H-Human
- M-Mouse
- R-Rat
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
GluD1/GRID1 (E4Y3N) Rabbit mAb recognizes endogenous levels of total GluD1/GRID1 protein.
Species Reactivity:
Human, Mouse, Rat
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Pro429 of human GluD1/GRID1 protein.
Background
Glutamate receptor ionotropic, delta-1 and delta-2 (GluD1 and GluD2, respectively) are part of the delta family of ionotropic glutamate receptors (iGluRs). Ionotropic receptors, which are typically cation-permeable ligand-gated ion channels, mediate most excitatory transmission in the brain (1). iGluR classes are defined based on sequence identity and pharmacological properties and include α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, kainate receptors, and N-methyl-D-aspartate (NMDA) receptors (2). Although GluDs were identified based on sequence identity and their structure is related to other iGluRs, GluDs do not bind glutamate and are unlikely to form ion channels like other iGluRs (3).
GluD1 and GluD2 share 56% sequence homology. While GluD2 expression is highest in the cerebellum and likely regulates motor function, GluD1 is expressed throughout the forebrain. While GluDs may not function like typical ligand-gated ion channels, they bind to other synaptic proteins and may function to alter subcellular expression of synaptic proteins, including other iGluRs as well as synaptic adhesion proteins. Genetic studies in mice suggest GluDs function in higher-order functions, including learning and memory, as well as addiction.
GluD1 and GluD2 share 56% sequence homology. While GluD2 expression is highest in the cerebellum and likely regulates motor function, GluD1 is expressed throughout the forebrain. While GluDs may not function like typical ligand-gated ion channels, they bind to other synaptic proteins and may function to alter subcellular expression of synaptic proteins, including other iGluRs as well as synaptic adhesion proteins. Genetic studies in mice suggest GluDs function in higher-order functions, including learning and memory, as well as addiction.
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For Research Use Only. Not For Use In Diagnostic Procedures.
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