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Thermo Fisher Scientific Phospho-NMDAR2B (Ser1303) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-NMDAR2B (Ser1303) Polyclonal Antibody

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Phospho-NMDAR2B (Ser1303) 폴리클로날 항체로 인간, 마우스, 랫트 시료에 반응. Western blot에 적합하며, 신경계 관련 단백질 인산화 연구에 활용. 고순도 친화 크로마토그래피 정제, PBS/glycerol 저장용액, -20°C 보관.

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마지막 업데이트 2025. 08. 02. 오후 02:11
Thermo Fisher Scientific PA537590 Phospho-NMDAR2B (Ser1303) Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-NMDAR2B (Ser1303) Polyclonal Antibody

Thermo Fisher Scientific Phospho-NMDAR2B (Ser1303) Polyclonal Antibody

Applications

  • Western Blot (WB)

Tested Dilution: 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Peptide sequence around phosphorylation site of Serine 1303 (Q-H-S(p)-Y-D) derived from Human GRIN2B
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2554198

Product Specific Information

A suggested positive control for Western blot is mouse brain cells.

Target Information

NMDAR2B is a member of the N-methyl-D-aspartate (NMDA) class of ionotropic glutamate receptors. NMDA receptors (NMDAR) are involved in long-term potentiation, an activity-dependent increase in synaptic transmission efficiency that underlies memory and learning.
NMDAR2B plays a role in neuronal development and has been implicated in central nervous system disorders such as Alzheimer’s disease, epilepsy, and ischemic neuronal cell death.
Overexpression of the NR2B subunit is associated with enhanced learning and memory, while reduced expression is observed in aged, memory-impaired animals. Phosphorylation at Tyr1472 may increase NMDAR expression at synapses, contributing to synaptic plasticity.
NMDAR2B forms a heterotrimeric complex with NR1, NR2, and NR3 subunits. Dysfunction is linked to epileptic encephalopathy and autosomal dominant mental retardation.

Usage Note

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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