Skip to main content

GABA-A R beta 1 Products

GABA A (γ-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. GABA A receptors are heteropentamer combinations of seven subunit types; α, β, γ, δ, ε, θ, and π. Three subunits, α, β, and γ, have at least three separate gene products in mammals, and typical GABA A receptors have some combination of α, β, and γ subunits.

The rat β1 isoform is a 58 - 60 kDa, 449 amino acid (aa), 4 transmembrane protein with two terminal extracellular regions. The ligand-binding region is in the N-terminus (aa 13 - 218). The β1 subunit is known to be phosphorylated on a consensus phosphorylation site (S409 of the precursor) that exists in the cytoplasmic domain between transmembrane segments 3 and 4. PKA or PKC βII-induced phosphorylation decreases GABA A receptor activity.

Show More

18 results for "GABA-A R beta 1" in Products

18 results for "GABA-A R beta 1" in Products

GABA-A R beta 1 Products

GABA A (γ-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. GABA A receptors are heteropentamer combinations of seven subunit types; α, β, γ, δ, ε, θ, and π. Three subunits, α, β, and γ, have at least three separate gene products in mammals, and typical GABA A receptors have some combination of α, β, and γ subunits.

The rat β1 isoform is a 58 - 60 kDa, 449 amino acid (aa), 4 transmembrane protein with two terminal extracellular regions. The ligand-binding region is in the N-terminus (aa 13 - 218). The β1 subunit is known to be phosphorylated on a consensus phosphorylation site (S409 of the precursor) that exists in the cytoplasmic domain between transmembrane segments 3 and 4. PKA or PKC βII-induced phosphorylation decreases GABA A receptor activity.

Show More

Recombinant Monoclonal Antibody

Reactivity: Human, Mouse, Rat
Details: Rabbit IgG Monoclonal Clone #SR1833
Applications: WB
Reactivity: Mouse, Rat
Details: Rabbit IgG Polyclonal
Applications: IHC, WB
Western Blot: GABA-A R beta 1 Antibody [NB300-197]
(2)
Reactivity: Human
Details: Rabbit IgG Polyclonal
Applications: IHC
Immunohistochemistry-Paraffin: GABA-A R beta 1 Antibody [NBP2-14034]
Applications: WB, ELISA, MA, AP

Recombinant Monoclonal Antibody

Reactivity: Human, Mouse, Rat
Details: Rabbit IgG Monoclonal Clone #1Q3A9
Applications: WB
Western Blot: GABA-A R beta 1 Antibody (1Q3A9) [NBP3-15857]
Applications: WB
Western Blot: GABA-A R beta 1 Overexpression Lysate [NBL1-10920]
Applications: AC

Competitive and selective GABAA antagonist

Alternate Names: Gabazine
Chemical Name: 6-Imino-3-(4-methoxyphenyl)-1(6H)-pyridazinebutanoic acid hydrobromide
Purity: ≥98% (HPLC)
Competitive and selective GABAA antagonist

Positive allosteric modulator of GABAA receptors

Alternate Names: 3a,5a-THPROG
Chemical Name: (3α,5α)-3-Hydroxy-pregnan-20-one
Positive allosteric modulator of GABAA receptors

GABAA agonist

Alternate Names: Gaboxadol
Chemical Name: 4,5,6,7-Tetrahydroisoxazolo[5,4-c]pyridin-3-ol hydrochloride
Purity: ≥98% (HPLC)
GABAA agonist

Benzodiazepine inverse agonist

Chemical Name: N-Methyl-β-carboline-3-carboxamide
Purity: ≥99% (HPLC)
Benzodiazepine inverse agonist

GABAA partial agonist; displays subtype selectivity

Chemical Name: 3-(2,5-Difluorophenyl)-7-(1,1-dimethylethyl)-6-[(1-methyl-1H-1,2,4-triazol-5-yl)methoxy]-1,2,4-triazolo[4,3-b]pyridazine
Purity: ≥98% (HPLC)
GABAA partial agonist; displays subtype selectivity

Postitive allosteric modulator of GABAA receptors

Chemical Name: (3α,5β)-3-Hydroxy-pregnan-20-one
Postitive allosteric modulator of GABAA receptors

α5-selective GABAA inverse agonist

Chemical Name: 3-(1,1-Dimethylethyl)-7-(5-methyl-3-isoxazolyl)-2-[(1-methyl-1H-1,2,4-triazol-5-yl)methoxy]-pyrazolo[1,5-d][1,2,4]triazine
Purity: ≥98% (HPLC)
α5-selective GABAA inverse agonist

Benzodiazepine antagonist

Alternate Names: Ro 15-1788
Chemical Name: 8-Fluoro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid, ethyl ester
Purity: ≥99% (HPLC)
Benzodiazepine antagonist

Potent and selective postitive allosteric modulator of GABAB receptors

Chemical Name: 5,7-Bis(1,1-dimethylethyl)-3-hydroxy-3(trifluoromethyl)-2(3H)-benzofuranone
Purity: ≥98% (HPLC)
Potent and selective postitive allosteric modulator of  GABAB receptors

Active metabolite of oxcarbazepine (Cat. No. 3864)

Alternate Names: GP 47779
Chemical Name: 10,11-Dihydro-10-hydroxy-5H-dibenz(Z)[b,f]azepin-5-carboxamide
Purity: ≥98% (HPLC)
Active metabolite of oxcarbazepine (Cat. No. 3864)
Results Per Page
5 10 25 50
/ 1