Immunological Sciences

Phospho-NMDAR1-S890

Western blot analysis of extracts of C6 cells, using Phospho-GRIN1-S890 antibody at 1:1000 dilution. C6 cells were treated by PMA/TPA (200nM) for 30 minutes after serumstarvation overnight. Secondary antibody: HRP Goat Anti- Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA. Detection: ECL Basic Kit. Exposure time: 90s.

Western blot analysis of extracts of C6 cells, using Phospho-GRIN1-S890 antibody at 1:1000 dilution. C6 cells were treated by PMA/TPA (200nM) for 30 minutes after serumstarvation overnight. Secondary antibody: HRP Goat Anti- Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA. Detection: ECL Basic Kit. Exposure time: 90s.

Catalog Number:ABP-0826
Conjugate:Unconjugated
Size:100 ug
Concentration:1mg/ml
Host:Rb
Isotype:IgG
Clone:Poly
Immunogen:A phospho specific peptide corresponding to residues surrounding S890 of human GRIN1.
Reactivity:Hu, Rt
Applications:WB 1.1000
Molecular Weight:Observed MW: 140kDaCalculated MW: 99kDa/101kDa/103kDa/105kDa/106kDa/107kDa
Purification:Affinity purification
Form:liquid
Synonyms:GluN1,MRD8,NMD-R1,NMDA1,NMDAR1,NR1

Applications

WB 1.1000

Immunogen

A phospho specific peptide corresponding to residues surrounding S890 of human GRIN1.

Target Background

The protein encoded by this gene is a critical subunit of N-methyl-D-aspartate receptors, members of the glutamate receptor channel superfamily which are heteromeric protein complexes with multiple subunits arranged to form a ligandgated ion channel. These subunits play a key role in the plasticity of synapses, which is believed to underlie memory and learning. Cell-specific factors are thought to control expression of different isoforms, possibly contributing to the functional diversity of the subunits. Alternatively spliced transcript variants have been described.

Synonyms:GluN1,MRD8,NMD-R1,NMDA1,NMDAR1,NR1

Storage

Store at -20℃. Avoid freeze / thaw cycles.

Buffer

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Western blot analysis of extracts of C6 cells, using Phospho-GRIN1-S890 antibody at 1:1000 dilution. C6 cells were treated by PMA/TPA (200nM) for 30 minutes after serumstarvation overnight. Secondary antibody: HRP Goat Anti- Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA. Detection: ECL Basic Kit. Exposure time: 90s.

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