GRIK2 anticorps (C-Term, Intracellular)
Aperçu rapide pour GRIK2 anticorps (C-Term, Intracellular) (ABIN7043238)
Antigène
Voir toutes GRIK2 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- C-Term, Intracellular
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Fonction
- A Rabbit Polyclonal Antibody to Kainate Receptor GluK2
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Réactivité croisée
- Humain, Souris, Rat
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Homologie
- Human,mouse,dog - identical
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Attributs du produit
- Anti-GRIK2 (GluK2) Antibody (ABIN7043238, ABIN7044336 and ABIN7044337) is directed against the intracellular C-terminus domain of the rat kainate receptor GluK2. The antibody can be used in western blot and immunofluorescence applications and will recognize GluR6 from rat, human and mouse origins.
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Purification
- Affinity purified on immobilized antigen.
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Immunogène
- CSAMVEELRMSLK, corresponding to amino acid residues 858-870 of rat kainate receptor GluK2
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Isotype
- IgG
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Indications d'application
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WB: 1:400
FC: The optimal concentration should be determined by the user
ICC: 1:400
IHC: The optimal concentration should be determined by the user
IP: The optimal concentration should be determined by the user
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Commentaires
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Negative Control: (ABIN7235657)
Blocking Peptide: (ABIN7235657)
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- 25 μL, 50 μL or 0.2 mL double distilled water (DDW), depending on the sample size.
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Concentration
- 0.8 mg/mL
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Buffer
- PBS pH 7.4, 1 % BSA with 0.05 % sodium azide
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C
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- GRIK2 (Glutamate Receptor, Ionotropic, Kainate 2 (GRIK2))
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Autre désignation
- GRIK2
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Sujet
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Synonyms: Glutamate receptor ionotropic kainate 2, Glutamate receptor 6, GluR6, GLUK6
Description: L-Glutamate, the major excitatory neurotransmitter in the central nervous system (CNS), operates through several receptors that are categorized as ionotropic (ligand-gated cation channels) or metabotropic (G-protein-coupled receptors).The ligand-gated ion channel family consists of fifteen members that have been subdivided into three families based upon their pharmacological profile: the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-preferring receptors, the N-methyl-D-aspartate (NMDA)-preferring receptors, and the kainate-preferring receptors.The kainate receptor subfamily consists of five members that have been further subdivided into two classes based upon structural homology and functional characteristics. GluR5, GluR6, and GluR7 receptor subunits share a high degree of homology and are able to form functional channels when expressed in heterologous systems. The KA-1 and KA-2 receptors are unable to form functional channels on their own, but when coexpressed with GluR5-7 receptor subunits, they form channels with high affinity for kainate.1,2Like AMPA receptors, the functional unit of endogenous kainate receptors is believed to be a tetramer, which can be either homomeric or heteromeric. Kainate receptors GluR5 and GluR6 (but not GluR7, KA-1, or KA-2) can undergo RNA editing, as in the AMPA receptor GluR2, a glutamine (Q) residue in the channel pore is edited to encode arginine (R) in the mature protein. Substitution of Q with R modulates the properties of the channel, producing channels with reduced single channel conductance and lower permeability to Ca2+.1,2GluR6 is expressed in the CNS in basal ganglia, cerebellum, and hipoccampus, as well as in the spinal cord. The exact physiological role of GluR6 is unclear, but a role in controlling neuronal excitability, synaptic integration, and synaptic plasticity has been proposed.
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ID gène
- 54257
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NCBI Accession
- NM_001166247
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UniProt
- P42260
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Pathways
- Synaptic Membrane, Regulation of long-term Neuronal Synaptic Plasticity
Antigène
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