AbPlus™ Anti-GRIA2 Magnetic Beads (VS-0724-YC1054)

CAT#: VS-0724-YC1054

The AbPlus Anti-GRIA2 Magnetic Beads (VS-0724-YC1054) is an innovative affinity resin which is bound with anti-GRIA2 specific antibody. The beads were designed for small-scale affinity purification and immunoprecipitation (IP) of GRIA2 protein under native and denaturing conditions.

Gene Expression
Figure 1 Cerebral cortex Figure 2 Hippocampus Figure 3 RNA cell line category: Cell line enriched (SCLC-21H)

Specifications

  • Applications
  • Immunoprecipitation, Protein Purification
  • Matrix
  • Magnetic bead
  • Bead Ligand
  • Anti-GRIA2 specific antibody
  • Target
  • GRIA2
  • Immunogen
  • Synthetic peptide corresponding to the center region of the human GRIA2/GLUR2.
  • Target Species
  • Human, Mouse, Rat
  • Bead Capacity
  • 40 mg/mL
  • Bead size
  • 25 μm
  • Format
  • Suspension
  • Concentration
  • 2 mg/mL
  • Buffer
  • PBS, pH 7.4
  • Preservative
  • 0.1% Sodium azide
  • Storage
  • Stored at 4°C, and is stable for up to 2 years. Do not centrifuge, dry or freeze the magnetic beads.

Applications

  • Application Notes
  • The beads are in suspension and will settle upon storage. Prior to use, mix the vial gently (do not vortex) to ensure delivery of proper bead volume.

Target

  • Introduction
  • Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to a family of glutamate receptors that are sensitive to alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA), and function as ligand-activated cation channels. These channels are assembled from 4 related subunits, GRIA1-4. The subunit encoded by this gene (GRIA2) is subject to RNA editing (CAG->CGG; Q->R) within the second transmembrane domain, which is thought to render the channel impermeable to Ca(2+). Human and animal studies suggest that pre-mRNA editing is essential for brain function, and defective GRIA2 RNA editing at the Q/R site may be relevant to amyotrophic lateral sclerosis (ALS) etiology.
  • Alternative Names
  • GLUR2; GLURB; GluA2; HBGR2; NEDLIB; gluR-2; gluR-B; GluR-K2
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