Human Glutamate Receptor, Ionotropic, N-Methyl-D-Aspartate 2C (GRIN2C) ELISA Kit (96T)

Human Glutamate Receptor, Ionotropic, N-Methyl-D-Aspartate 2C (GRIN2C) ELISA Kit (96T)

Catalog #: TD3625
Availability: In Stock
¥649.00
Detection range: 0.312-20ng/mL    
Sensitivity: 0.118ng/mL    
Type: Traditional GRIN2C ELISA kit    
Synonyms: NMDAR2C; NR2C; Glutamate [NMDA] receptor subunit epsilon-3; N-methyl D-aspartate receptor subtype 2C
Species: Human
Sample type: tissue homogenates or other biological fluids.
Experimental method: Sandwich
Shelf life: 12 months
Gene ID: 2905
UniProt ID: Q14957
Components: 1. Pre-coated, ready to use 96-well strip plate 1
2. Plate sealer for 96 wells 2
3. Standard 2
4. Diluents buffer: 1×45 mL
5. Detection Reagent A: 1×120 μL
6. Detection Reagent B: 1×120 μL
7. TMB Substrate: 1×9 mL
8. Stop Solution: 1×6 mL
9. Wash Buffer (30× concentrate): 1×20 mL




Background

This gene encodes a member of the N-methyl-D-aspartate (NMDA) receptor family within the ionotropic glutamate receptor superfamily. The encoded protein is a subunit of the NMDA receptor ion channel which acts as an agonist binding site for glutamate. The NMDA receptors mediate a slow calcium-permeable component of excitatory synaptic transmission in the central nervous system. The NMDA receptors are heterotetramers of seven genetically encoded, differentially expressed subunits including NR1 (GRIN1), NR2 (GRIN2A, GRIN2B, GRIN2C, or GRIN2D) and NR3 (GRIN3A or GRIN3B). The early expression of this gene in development suggests a role in brain development, circuit formation, synaptic plasticity, and cellular migration and differentiation. Naturally occurring mutations within this gene are associated with neurodevelopmental disorders including autism spectrum disorder, attention deficit hyperactivity disorder, epilepsy, and schizophrenia.

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GRIN2C