18 results for "GPR55" in 产品

GPR55 Products

Members of the G protein-coupled receptor (GPCR) family, such as GPR55, play important roles in signal transduction from the external environment to the inside of the cell. GPR55 is a receptor for L-alpha-lysophosphatidylinositol (LPI). LPI induces Ca2+ release from intracellular stores via the heterotrimeric G protein GNA13 and RHOA. GPR55 is expressed in the caudate nucleus and putamen, but not detected in the hippocampus, thalamus, pons cerebellum, frontal cortex of the brain or in the liver. It is expressed in osteoclasts and osteoblasts. GPR55 may play a role in bone physiology by regulating osteoclast number and function. GPR55 may also be involved in hyperalgesia associated with inflammatory and neuropathic pain.

Reactivity: Human, Canine
Details: Rabbit IgG Polyclonal
Applications: IHC, WB
Immunohistochemistry: GPR55 Antibody - BSA Free [NB110-55498]
(6)
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Reactivity: Human
Details: Rabbit IgG Polyclonal
Applications: IHC
Immunohistochemistry-Paraffin: GPR55 Antibody - BSA Free [NLS6817]
(6)
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Reactivity: Human
Applications:
R&D Systems VersaClone cDNA Plasmids
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Reactivity: Mouse
Applications:
R&D Systems VersaClone cDNA Plasmids
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Reactivity: Mouse, Rat
Details: Rabbit IgG Polyclonal
Applications: WB, ELISA, ICC/IF
Western Blot: GPR55 AntibodyAzide and BSA Free [NBP3-04847]
(2)
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Reactivity: Human
Applications: WB
Western Blot: GPR55 Overexpression Lysate [NBL1-11284]
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Reactivity: Human
Details: Rabbit IgG Polyclonal
Applications: WB
Western Blot: GPR55 Antibody [NBP2-99403]
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Reactivity: Mouse, Rat
Details: Rabbit Polyclonal
Applications: WB
Novus Antibodies
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Potent CB1 antagonist; also GPR55 agonist

Chemical Name: N-(Piperidin-1-yl)-5-(4-iodophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide
Purity: ≥98%
Potent CB1 antagonist; also GPR55 agonist
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Selective GPR55 agonist. FAAH and PAA substrate

Alternate Names: PEA
Chemical Name: N-(2-Hydroxyethyl)hexadecanamide
Selective GPR55 agonist. FAAH and PAA substrate
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Potent GPR55 agonist

Chemical Name: 5-Methyl-4-[(1R,6R)-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-1,3-benzenediol
Purity: ≥97%
Potent GPR55 agonist
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Potent, selective GPR55 antagonist

Alternate Names: CID 1261822
Chemical Name: N-[4-[[(3,4-Dimethyl-5-isoxazolyl)amino]sulfonyl]phenyl]-6,8-dimethyl-2-(2-pyridinyl)-4-quinolinecarboxamide
Purity: ≥98%
Potent, selective GPR55 antagonist
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Selective GPR55 antagonist

Chemical Name: 4-[4,6-Dihydro-4-(3-hydroxyphenyl)-3-(4-methylphenyl)-6-oxopyrrolo[3,4-c]pyrazol-5(1H)-yl]benzoic acid
Purity: ≥98%
Selective GPR55 antagonist
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Lipid mediator, anorexic actions; also GPR55 and PPARα agonist

Chemical Name: (9Z)-N-(2-Hydroxyethyl)-9-octadecenamide
Purity: ≥99%
Lipid mediator, anorexic actions; also GPR55 and PPARα agonist
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Selective GPR55 agonist; also promotes NSC proliferation and differentiation

Alternate Names: CID 20440433
Chemical Name: 3-[[4-(2,3-Dimethylphenyl)-1-piperazinyl]carbonyl]-N,N-dimethyl-4-(1-pyrrolidinyl)benzenesulfonamide
Purity: ≥98%
Selective GPR55 agonist; also promotes NSC proliferation and differentiation
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Natural cannabinoid; GPR55 antagonist, weak CB1 antagonist, CB2 inverse agonist and AMT inhibitor

Alternate Names: CBD
Chemical Name: 2-[(1R,6R)-3-Methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol
Purity: ≥98%
Natural cannabinoid; GPR55 antagonist, weak CB1 antagonist, CB2 inverse agonist and AMT inhibitor
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Endogenous and non-selective CB agonist; potent GPR55 agonist

Alternate Names: 2-AG,Arachidonoylglycerol
Chemical Name: (5Z,8Z,11Z,14Z)-5,8,11,14-Eicosatetraenoic acid, 2-hydroxy-1-(hydroxymethyl)ethyl ester
Endogenous and non-selective CB agonist; potent GPR55 agonist
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Endogenous and non-selective CB agonist

Alternate Names: Arachidonylethanolamide,AEA
Chemical Name: N-(2-Hydroxyethyl)-5Z,8Z,11Z,14Z-eicosatetraenamide
Purity: ≥98%
Endogenous and non-selective CB agonist
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