GABA-A R beta 2 C-Terminus Antibody Summary
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of GABAAR beta 2 C-Terminus by Western Blot. Western blot of 5 - 7 μg rat brain (cerebellum) lysates. The blot was incubated overnight at 2 - 8° C with anti-GABAAR beta 2 subunit, C-Terminus diluted 1:1000. The antibody labeled the ~50 - 56 kDa beta 2 subunit of the GABAAR.
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Preparation and Storage
Background: GABA-A R beta 2
GABAA ( gamma -aminobutyric acid-type A) receptors are members of the cysteine-loop family of neurotransmitter-gated ion channels. GABA binding to A-type receptors induces anion-selective ion channel opening. These receptors are the principal fast inhibitory neurotransmitter receptors in the CNS. GABAA receptors are heteropentamer combinations of seven subunit types; alpha, beta, gamma, δ, epsilon, theta, and π. Three subunits, alpha, beta, and gamma, have at least three separate gene products in mammals, and typical GABAA receptors have some combination of alpha, beta and gamma subunits. The rat beta 2 isoform is a 55 kDa, 450 amino acid (aa), 4 transmembrane protein with two terminal extracellular regions. The ligand-binding region is in the N-terminus (aa 13 - 218). The beta 2 subunit is part of the most common GABAA receptor combination in the mammalian brain ( alpha 1 beta 2 gamma 2). Like the other two beta subunits, beta 2 is phosphorylated on a consensus phosphorylation site (S410 of the precursor) that exists in the second cytoplasmic domain. In contrast to the other beta sub-units, only PKC is capable of this modification. However, tyrosine phosphorylation of beta 2 is known, and this apparently increases GABAA current amplitude.
- Darlison, M.G. et al. (2005) Cell. Mol. Neurobiol. 25:607.
- Akabas, M.H. (2004) Int. Rev. Neurobiol. 62:1.
- Song, M. and R.O. Messing (2005) Cell. Mol. Life Sci. 62:119.
- Brandon, N.J. et al. (2002) J. Neurosci. 22:6353.
- McDonald, B.J. et al. (1998) Nat. Neurosci. 1:23.
- Wan, Q. et al. (1997) J. Neurosci. 17:5062.
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