Phospho-NMDAR2B (Ser1303) Rabbit pAb
Cat#:DPA05414应用:WB,ICC/IF
Product Name: | Phospho-NMDAR2B (Ser1303) Rabbit pAb |
Cat No.: | DPA05414 |
Clonality: | Polyclonal |
Species Reactivity: | Human, Mouse, Rat |
Tested Applications: | WB,ICC/IF |
Recommended Dilution: | WB: 1:1000 ICC/IF: 1:20 |
Size: | 30ul 50ul 100uL |
Format: | Liquid |
Source: | Rabbit |
Purification Method: | Affinity Purification |
Isotype: | IgG |
Conjugate: | Un-conjugated |
Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
Immunogen: | A synthetic phosphopeptide corresponding to residues surrounding Ser1303 of human NMDAR2B |
Calculated Molecular Weight: | 166 kDa |
Observed Molecular Weight: | 200 kDa |
GenBank Accession Number: | Q13224 |
Gene ID (NCBI): | 2904 |
Synonyms: | NR3; MRD6; NR2B; hNR3; EIEE27; GluN2B; NMDAR2B |
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. [provided by RefSeq, Aug 2017] |
Category: | Primary Ab |