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GluR1 (phospho Ser845) Antibody

Product Specifications

Background

The ion channels activated by glutamate are typically divided into two classes. Those that are sensitive to N-methyl-D-aspartate (NMDA) are designated NMDA receptors (NMDAR) while those activated by alpha-amino-3-hydroxy-5-methyl-4-isoxalone propionic acid (AMPA) are known as AMPA receptors (AMPAR) . The AMPAR are comprised of 4 distinct subunits (GluR1-4) and they play key roles in virtually all excitatory neurotransmission in the brain. The GluR1 subunit is widely expressed throughout the nervous system. GluR1 is also potentiated by phosphorylation at Ser845. In addition, phosphorylation of this site has been linked to synaptic plasticity as well and learning and memory.

NCBI Gene ID

50592

Swiss Prot

P19490

Accession Number

P19490

Host

Rabbit

Reactivity

Human, Mouse, Rat

Immunogen

GluR1 (Ser845) polyclonal antibody was raised against a synthetic phosphopeptide corresponding to amino acids residues surrounding the phospho-Ser845 of rat GluR1.

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Neuroscience, Phospho-Specific

Purification

Affinity Purified

Concentration

Batch dependent

Modification

Phospho-Specific

Shipping Conditions

Blue Ice

Storage Conditions

For long term storage –80˚ C is recommended, but shorter term storage at –20˚ C is also acceptable as aliquots may be taken without freeze/thawing due to the presence of 50% glycerol. Stable for one year.

Calculated Molecular Weight

100

Specificity

GluR1 antibody is specific for GluR1 phosphorylated at Ser845.

Applications Notes

Immunolabeling of the GluR1 protein in western blots of rat brain is blocked by the Ser845 phosphopeptide used as antigen but not by the corresponding non-phosphopeptide. The antibody is purified by sequential chromatography on phospho- and non-phosphopeptide affinity columns. Antibody dilutions and tissue load should be based on tissue type and expected phosphorylation state. Initial recommended range of dilutions: 1:500 to 1:2000. Applications include Immunofluorescence (IF), Immunohistochemistry (IHC) and Western Blots (WB) . Immunohistochemistry (IHC) has not yet been determined. Human, mouse and rat have 100% amino acid sequence identity with the antigen used to raise the antibody. When internally tested under ideal conditions the working dilutions were 1:1000 for IF, IHC and WB.

Symbol

Gria1

NCBI Official Name

Glutamate receptor, ionotropic, AMPA 1

NCBI Organism

Rattus norvegicus

Background Reference 01

Roche, K.W., O'Brien, R.J., Mammen, A.L., Bernhardt, J., and Huganir, R.L., "Characterization of multiple phosphorylation sites on the AMPA receptor GluR1 subunit, " Neuron, 16 (1996) 1179 - 1188.

Background Reference 02

Blackstone, C.D., Moss, S.J., Martin, L.J., Levey, A.I., Price, D.L. and Huganir, R.L., "Biochemical characterization and localization of a non-N- methyl-D-aspartate glutamate receptor in rat brain, " J. Neurochem. 58 (1992) 1118 - 1126.

Background Reference 03

McGlade-Mcculloh, E., Yamamoto, H., Tan, S.-E., Brickey, D.A. and Soderling, T.R. "Phosphorylation and regulation of glutamate receptors by calcium/calmodulin-dependent protein kinase II, " Nature (London) 362 (1993) 640 - 642.

Background Reference 04

Barria, A., Muller, D., Derkach, V., Griffith, L.C. and Soderling, T.R., "Regulatory phosphorylation of AMPA-type glutamate receptors by CaM-KII during long-term potentiation, " Science 276 (1997) 2042 - 2045.

Tested Applications

WB, IF, IHC

Protein ID

97536283

Physical Properties

Liquid

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