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GRIN1/NMDAR1 Products

NMDA receptors (NMDARs) are members of the glutamate-gated ion-channel family and function in synaptic plasticity, neuronal development and excitotoxicity. NMDARs are heteromeric complexes of multiple subunits: NR1, which occurs as eight distinct isoforms as the result of alternate splicing; NR2 (NR2A, B, C and D are encoded by four related genes, several of which also display multiple splice forms); and NR3 (NR3A and B also have several splice forms). The particular combination of subunits determines the functional characteristics of the receptor.

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32 results for "GRIN1/NMDAR1" in Products

32 results for "GRIN1/NMDAR1" in Products

GRIN1/NMDAR1 Products

NMDA receptors (NMDARs) are members of the glutamate-gated ion-channel family and function in synaptic plasticity, neuronal development and excitotoxicity. NMDARs are heteromeric complexes of multiple subunits: NR1, which occurs as eight distinct isoforms as the result of alternate splicing; NR2 (NR2A, B, C and D are encoded by four related genes, several of which also display multiple splice forms); and NR3 (NR3A and B also have several splice forms). The particular combination of subunits determines the functional characteristics of the receptor.

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Applications: WB, IHC
Reactivity: Human, Mouse, Rat
Applications: ICC, ICFlow
Reactivity: Mouse
Applications: WB, IHC
Reactivity: Mouse, Rat
Applications: WB, IP
Reactivity: Human, Mouse, Rat
Applications: ICFlow
Reactivity: Mouse
Applications: WB, IHC
Reactivity: Mouse, Rat
Applications: WB, IHC
Reactivity: Mouse, Rat
Applications: ICFlow
Reactivity: Mouse
Applications: ICFlow
Reactivity: Mouse
Applications: ICFlow
Reactivity: Mouse
Applications: ICFlow
Reactivity: Mouse
Applications: ICFlow
Reactivity: Mouse
Applications: ICFlow
Reactivity: Mouse

Potent and selective NMDA receptor antagonist; more active form of DL-AP5

Potent and selective NMDA antagonist

Non-competitive NMDA antagonist; acts at ion channel site

Broad spectrum glutamatergic antagonist

NMDA antagonist; antidepressant; may not display psychotomimetic or addictive side effects of (S)-ketamine

Potentiator of NMDA recepors; acts at glycine site

GluN1/GluN2A-selective NMDA antagonist

Potent NMDA antagonist; acts at glycine site

Potent and selective NMDA antagonist; acts at glycine site

Specific σ ligand, NMDA antagonist

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